Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:The candidate would be expected to assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients. The candidate would be required to stay current on air quality regulations. This position is in Shaw?s Environmental and Infrastructure division, air quality consulting group. The hired person will work closely with mangers at their office location and Shaw?s National Practice Leader for Air Quality Consulting.Responsibilities:•The candidate will assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients.•The candidate will be required to stay current on air quality regulations.•Work activities will include developing emission calculations (criteria pollutants, hazardous air pollutants and greenhouse gases), gathering technical data from clients and through independent research, determining regulatory requirements (e.g. NSPS, NESHAP, and NSR/PSD) for emission sources, and assisting in preparing compliance and permitting documents.•Additional responsibilities will include calculating emissions to determine health risk impacts using various emission models and documenting the results in a technical report.• Candidate may be located at client sites for extended period of time•Candidate will work closely with Project Managers in implementing project tasks.•Candidate must be flexible and willing to support other non-air related projects as needed.Qualifications/Competencies/Experience:•The required/minimum qualifications MUST be demonstrated/documented on the resume submitted to Shaw.•Must have BS degree in chemical, petroleum, environmental, or mechanical engineering and 3 years of environmental work experience,•Must have at least 2 years of air permitting & compliance experience, including direct technical work on at least one PSD/Title V air permit application.•Must have proficiency in Microsoft Office: Word, Excel, and PowerPoint.•Must have effective written and verbal communication skills.•Must have knowledge and understanding of local, state, and federal air quality regulations (Texas experience preferred).•Ability to work independently as well as in a team environment, strict attention to detail.•Excellent time management skills to manage multiple activities on an on-going basis within provided deadlines.•Must be authorized to work in the United States.•Preference will be given to candidates with Air Quality experience in Oil and Gas Upstream and Midstream operations.
Monday, 30 July 2012
Environmental Engineer / Scientist
Details: Conestoga-Rovers & Associates (CRA) provides comprehensive engineering, environmental consulting, construction, and information technology solutions for our clients. With more than 30 years of experience in providing high quality and responsive services, CRA has grown to over 90 offices and 3,000 employees working on projects worldwide.Conestoga-Rovers & Associates has an opening in our Baton Rouge, LA for an Environmental Engineer or Scientist, who aspires to become an active employee in a vibrant, well-established company. If you’re driven, fast track your career here. Responsibilities include• Data compilation, reduction, interpretation, evaluation/comparison to environmental regulatory standards. Preparation of emissions calculations using standard factors or operational data• Interpretation and implementation of environmental regulations, including: Title V, NSPS/NESHAPs, NPDES, UIC, and RCRA• Active participation in business development activities, including client meetings, preparation of business development material, training and professional organizations• Projects may include:• NNSR and PSD Air Permitting• Title V and State Air Permitting and Compliance• Compliance Assurance and auditing• Regulatory Applicability Analysis• Emissions Inventory• Compliance Database Development, Design, and Implementation• LPDES Permitting• RCRA Permitting • Spill Prevention Control and Countermeasures Plans (SPCC)• Facility Response Plans• Storm Water Pollution Plans (SWPPP)
LAB TECHNICIAN
Details: Position 1--Conducts chemical and physical laboratory tests of solid materials, liquids, and gases, and analyzes test data for variety of purposes, such as research, product development, quality control, criminal investigation, and establishing standards, involving experimental, theoretical, or practical application of chemistry and related sciences: Sets up laboratory equipment and instrumentation required for tests, research, or process control. Tests and analyzes products to determine strength, stability, purity, chemical content, and other characteristics. Documents results of tests and analyses.Pay rate is at $11/hour
Radiological Engineer
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:Performs a variety of technical work on all phases of projects, specifically in the areas of radiation protection and radiological operations.Responsibilities:Work activities include, but are not limited to, the following:Collection and interpretation/evaluation of scientific dataDevelopment of plans, specifications, analyses, evaluations, maps, position papers, procedures and reports. Communication of technical concepts, evaluation results, plans, reports, etc. via oral presentations; and ensures conformance to applicable technical standards as well as company policies and procedures. All scientific disciplines outside of engineering are included in this job family. In E&I, encouraged to apply for and become a Senior Technical Leader in the Technical Leadership programQualifications/Competencies/Experience:Background in Health Physics preferred. CHP not required but a plusStrong technical writing skills a must. Candidates will be asked to provide a 1st draft writing sampleIs recognized as an expert in own area within the organizationProvides leadership, mentoring and guidance to othersIs a lead contributor; may participate in development of business strategyProgression to this level is typically restricted based on business requirementsHas developed depth of expertise in own discipline and broad knowledge of other disciplinesApplies expertise to the most complex problems; coordinates work outside own area of expertiseAnticipates customer needs to influence the development of innovative solutionsAnticipates internal/external business and regulatory issues; recommends process/product improvementsManages resource requirements and business needs for projectsAnticipates problems; develops innovative solutions and ensures solutions are consistent with organizational objectivesDevelops and manages plans to achieve objectives; participates in the development of business strategyPresents highly complex ideas and anticipates potential objections; influences othersTakes leadership role; acts as a facilitator and mentor. Typically has 10 to 25+ years of relevant experience.
Postdoctoral Scientist
Details: Astellas is the bright spot in the pharmaceutical industry -- not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. A high standard of ethics is mandatory. Quality is our pledge. Diversity is valued. Individual initiative is rewarded. Astellas offers an environment where our employees can make a real difference. Come, shine with us! The goal of the Postdoctoral Scientist position is to provide a 2 year temporary industrial training experience for a recent Ph.D. graduate. The Postdoctoral Scientist will contribute scientific insight and expertise to ongoing research projects at Urogenix. In return, Urogenix will provide scientific training in, and exposure to, a dynamic preclinical pharmaceutical research environment. Specifically, the Postdoctoral Scientist will perform cellular pharmacology research in support of new or ongoing research projects pertaining to the electrophysiological and pharmacological characterization of visceral smooth muscle cells in normal as well as in pathological conditions. This scientist will plan, direct and conduct research using primarily in vitro electrophysiological and/or calcium imaging techniques. Other techniques, such as in vitro smooth muscle contractility, histology, molecular biology, and in vivo techniques will be used as needed. In addition, this scientist will be responsible for the development of experimental protocols, execution of pharmacological experiments, analysis of data and presentation of results. These duties will require a high degree of independence, along with collaborative interactions with other Urogenix scientists. The Postdoctoral Scientist will report directly to the In vivo team leader at Urogenix and will not directly supervise other scientists. This position requires a Ph.D. degree preferably in the biomedical or pharmaceutical sciences. As this is a training position, a recent graduate is preferred. In addition, experience with smooth muscle physiology is desirable. •cb*
Radiation Safety Officer (RSO)
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:Performs a variety of Project Management and Scientific work on all phases of projects, but has a specialty in radiological project operations and management. Other duties may be assigned.Responsibilities:Work activities include but are not limited to supervision of two or more Scientists, collection and interpretation/evaluation of scientific data, development of plans, specifications, analyses, maps, position papers, procedures and reports, communication of technical concepts, evaluation results, plans, reports, etc., via oral presentations.Ensures conformance to applicable technical standards as well as company policies and procedures.Position supervises the on-site radioanalytical laboratory.Conduct radiological worker training for project staff, and conduct periodic professional development and refresher training for Radiological Controls Technicians.Acts as a key contributor in a complex and critical environment.May lead teams or projects; shares expertise.Applies in-depth skills and broad knowledge of the business to address complex problems and nonstandard situations.Anticipates customer needs and identifies solutions.Interprets internal/external business issues and recommends best practices in own discipline.Manages costs for specific projects.Solves complex problems; takes a broad perspective to identify innovative solutionsManages own time to meet objectives; forecasts and plans resource requirements.Explains difficult concepts and persuades others to adopt a point of view.Motivates other team members; may be team leader.Administers a H&S continuous improvement process applicable to industrial H&S and radiation protection.Applies expertise to create financial and operational solutions that apply across multiple functional areas.Influences customers and/or organizational leadership to accomplish operational objectives.Shapes and integrates functional strategies while anticipating demands to align operational priorities.Develops and leverages relationships with key internal/external customers to identify and support business needs.Negotiates with and /influences customers and/or organizational leadership to set priorities and solidify relationships.Verifies company and client compliance with Environmental Health and Safety policies, Standards and Regulations for Radiation Protection, Occupational Safety and Health Administration regulations, and other job-specified procedures or standards.Identifies business issues that may impact organizational results.Develops plans and budgets to achieve functional, cross-functional objectives or operational objectives.Manages and deploys resources to achieve financial and business objectives across multiple functional areas.Communicates, presents or justifies overall Health and Safety performance to management as necessary.May take active role presenting proposals to prospective clients. Leverages the performance management cycle to motivate employees and support achievement of objectives.Develops financial and operational objectives/plans to align with business objective within own area/function objectives within own area.Influences customer and/or organizational leadership to accomplish operational objectives.Directs the resolution of highly complex or unusual business problems that cross functional lines.Qualifications/Competencies/Experience:A B.S. or higher degree in Physics, Chemistry, Health Physics, or related field is desirable; however experience maybe evaluated in lieu of education.A candidate in possession or pursuit of Professional Certification (CHP, NRRPT) is desirable.Has depth and breadth of experience in own discipline; integrates knowledge of business and functional priorities.Experience and training with the design and implementation of Scoping, Characterization, and Final Status Surveys in accordance with MARSSIM.Experience supervising or managing radiological work for USACE and on a FUSRAP site is preferable.Familiar with radioanalytical methods and equipment.Familiar with typical portable radiological survey instruments and the determination of radionuclide specific efficiencies and minimum detectable concentrations (MDCs) suitable for project release criteria, action levels, investigation levels, or derived concentration guideline levels (DCGLs).Must be aware of federal, state and local safety laws to ensure the organization complies with all current safety regulations.Ability to explain difficult concepts while persuading other to adopt a common point of view is required.Requires 7 to 12 years relevant professional level experience dealing with issues related to radiation safety and remediation, and with operation and implementation of health physics programs to comply with the radiation protection regulations and standards of the USNRC, USDoD, USDOE, USACE and Agreement States.For assignments as a radiation safety officer, working knowledge of 10 CFR 20 and CCR 17 in support of implementing Shaw?s NRC and/or CA Radioactive Materials Service Licenses at project locations.A working knowledge of principles of radiation protection and federal and state regulatory requirements and standards for radiological safety, radiological emergency planning and response and radiological management is required.Familiar with standard radiation safety and health physics concepts, practices, and procedures within different regulatory jurisdictions as applicable to assignments, i.e., NRC, DOE, DOD, USACE, EPA.
Dallas Field Safety Specialist
Details: Pacesetter is a temporary labor service with 30 years of experience and "know how". Daily, we recruit, dispatch and deliver thousands of workers to businesses throughout the Southern United States. Our expertise is providing workers for manual labor, industrial and construction jobs. Whether you need, Pacesetter can fill the order. Most of our 70 dispatch offices never close. They are open 24 hours a day, 7 days a week, ready and able to fill orders A.S.A.P. Unlike the majority of our competitors, we operate 100 delivery vehicles to ensure that you can count on us to timely deliver workers to your doorstep. All workers provided by Pacesetter are our employees; therefore, our customers are able to enjoy the following benefits: We pay workers' compensation insurance premiums We pay general liability insurance premiums We pay social security taxes We pay federal and state withholding taxes We handle unemployment claims We process W-2's We maintain employee records such as I-9's and W-4's We remove the need for any "help wanted" advertising We remove the need for health insurance premiums We pay for all recruiting expenses At Pacesetter Personnel Services, we take pride in providing our employees and customers a safe work environment. We currently have an opportunity for a strong, experienced safety inspector. This position is for a reliable, self-starter in the Dallas Area, who will be required to travel to various different company and/or client sites to perform various inspections. The Safety Specialist's number one responsibility is to minimize injuries, reduce exposure to workplace hazards and comply with Company, customer and regulatory requirements. This individual will be responsible for driving a safety-minded culture and instilling it in our operations across multiple offices throughout the Dallas territory. Site inspections: Conduct risk assessments, identify potential hazards and safety needs at business sites and provide site-specific recommendations to reduce or eliminate risk. Assist in coordinating Insurance Inspections; Participate in periodic loss prevention inspections by insurance carriers and provide assistance with insurance claims.
Specialty Environmental Monitor
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Please review the below summary, responsibilities, and qualifications for this position.Summary:Performs a variety of scientific work on all phases of projects.Responsibilities:Inspects and monitors Contractor activities for compliance with environmental performance requirements in either or both biology or botany. Provides clearance of work areas for Threatened and Endangered species, prepares compliance reports and non-compliance and violation reports. Conducts pre-construction surveys and evaluates field changes and proposed variances for wildlife and botanical issues.Qualifications/Competencies/Experience:•Biologists or environmental scientist with a baccalaureate degree in appropriate field of specialty•Some field experience (especially in the area of environmental construction compliance) with either plants native to the San Francisco peninsula, or with animal species including but not limited to: dusky-footed woodrat, San Francisco Garter Snake, nesting birds or raptors, bats, Western pond turtles, or California Red-Legged Frogs is definitely a plus
Scientist
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:Performs a variety of scientific work on all phases of projects.Responsibilities:Job includes field efforts associated with Phase I and II environmental site assessments, auditing, SPCC inspections, construction storm water inspections, and groundwater monitoring. Field effors are approximately 60 percent of time in Louisiana, Mississippi, Alabama and Arkansas. Work activities include, but are not limited to, the following:Collection and interpretation/evaluation of scientific dataDevelopment of plans, specifications, analyses, evaluations, maps, position papers, procedures and reports. Communication of technical concepts, evaluation results, plans, reports, etc. via oral presentations; and ensures conformance to applicable technical standards as well as company policies and procedures. All scientific disciplines outside of engineering are included in this job family.Qualifications/Competencies/Experience:Preference is for Geology bachelors degree with 1 to 3 years experience. Has in-depth experience, knowledge and skills in own discipline. Works independently with minimal guidance. Usually determines own work priorities. Acts as a resource for colleagues with less experience. Has expertise in own discipline. Applies knowledge and skills to a wide range of standard and nonstandard situations. Interprets customer needs, assesses requirements and identifies solutions to non-standard requests. Uses best practices and knowledge of internal/external business issues to improve products or services in own discipline. Monitors and controls costs within own work. Solves moderately complex problems; takes a new perspective on existing solutions. Explains difficult issues and works to establish consensus.
Medical Technologist - Night Shift
Details: JOB SUMMARYPerforms laboratory assays on a variety of patient samples such as blood and body fluids, evaluates data for accuracy and appropriateness, and reports results to clinicians for patient diagnosis and treatment. MAJOR ACCOUNTABILITIES/CRITICAL RESPONSIBILITIES1. Follows all Laboratory and Hospital safety policies.2. Operates all department equipment safely and according to manufacturer guidelines. Performs preventative maintenance and troubleshoots instrument failures to best of ability alerting proper personnel of equipment problems.3. Follows all department QC procedures and troubleshoots QC failures with proper documentation.4. Takes part in inter and intra-department QA initiatives.5. Responds to department staffing needs by covering extra shifts when necessary.6. Maintains technical competency and seeks clarification when necessary.7. Effectively utilizes all necessary LIS functions.8. Assists supervisor in maintaining adequate inventory of reagents and supplies necessary for testing.9. Collects blood samples, accurately identifying and labeling patient sample according to laboratory policy. Utilizes proper phlebotomy techniques and appropriate specimen containers. 10. Meets performance expectations for Customer Service, Teamwork, Resource Utilization, and Staff and Self Development as outlined in performance review.11. Performs other duties as assigned or directed to ensure smooth operation of the department/unit. UNIT SPECIFIC RESPONSIBILITIES1. Performs and evaluates for accuracy all stat procedures in the Chemistry and Serology sections.2. Is able to prioritize stat testing to ensure optimal patient care.3. Follows laboratory guidelines with regards to reporting panic or critical lab results and is able to explain antibody problems or transfusion delays to clinicians.4. Performs and interprets routine and advanced immunohematologic procedures, such as types and screens antibody panels and antigen typings, as indicated.5. Prepares and issues appropriate blood and blood components for transfusion.6. Evaluates patients for RhIG candidacy and orders such appropriately.7. Performs and evaluates for accuracy all STAT and routine testing in the Hematology section.8. Using appropriate media, plates all cerebral spinal fluid cultures received on night shift.9. Performs Rapid Beta Strep screens, upon request.10. Prepares and stains gram stains for physician review, upon request.11. Performs Fetal Fibronectin testing, upon request.
Air Quality Specialist (Chemical/Environmental engineer)
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:The candidate would be expected to assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients. The candidate would be required to stay current on air quality regulations. This position is in Shaw?s Environmental and Infrastructure division, air quality consulting group. The hired person will work closely with mangers at their office location and Shaw?s National Practice Leader for Air Quality Consulting.Responsibilities:•The candidate will assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients.•The candidate will be required to stay current on air quality regulations.•Work activities will include developing emission calculations (criteria pollutants, hazardous air pollutants and greenhouse gases), gathering technical data from clients and through independent research, determining regulatory requirements (e.g. NSPS, NESHAP, and NSR/PSD) for emission sources, and assisting in preparing compliance and permitting documents.•Additional responsibilities will include calculating emissions to determine health risk impacts using various emission models and documenting the results in a technical report.• Candidate may be located at client sites for extended period of time•Candidate will work closely with Project Managers in implementing project tasks.•Candidate must be flexible and willing to support other non-air related projects as needed.Qualifications/Competencies/Experience:•The required/minimum qualifications MUST be demonstrated/documented on the resume submitted to Shaw.•Must have BS degree in chemical, petroleum, environmental, or mechanical engineering and 3 years of environmental work experience,•Must have at least 2 years of air permitting & compliance experience, including direct technical work on at least one PSD/Title V air permit application.•Must have proficiency in Microsoft Office: Word, Excel, and PowerPoint.•Must have effective written and verbal communication skills.•Must have knowledge and understanding of local, state, and federal air quality regulations (Texas experience preferred).•Ability to work independently as well as in a team environment, strict attention to detail.•Excellent time management skills to manage multiple activities on an on-going basis within provided deadlines.•Must be authorized to work in the United States.•Preference will be given to candidates with Air Quality experience in Oil and Gas Upstream and Midstream operations.
Air Quality Specialist (Chemical/Environmental engineer)
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:The candidate would be expected to assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients. The candidate would be required to stay current on air quality regulations. This position is in Shaw?s Environmental and Infrastructure division, air quality consulting group. The hired person will work closely with mangers at their office location and Shaw?s National Practice Leader for Air Quality Consulting.Responsibilities:•The candidate will assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients.•The candidate will be required to stay current on air quality regulations.•Work activities will include developing emission calculations (criteria pollutants, hazardous air pollutants and greenhouse gases), gathering technical data from clients and through independent research, determining regulatory requirements (e.g. NSPS, NESHAP, and NSR/PSD) for emission sources, and assisting in preparing compliance and permitting documents.•Additional responsibilities will include calculating emissions to determine health risk impacts using various emission models and documenting the results in a technical report.• Candidate may be located at client sites for extended period of time•Candidate will work closely with Project Managers in implementing project tasks.•Candidate must be flexible and willing to support other non-air related projects as needed.Qualifications/Competencies/Experience:•The required/minimum qualifications MUST be demonstrated/documented on the resume submitted to Shaw.•Must have BS degree in chemical, petroleum, environmental, or mechanical engineering and 3 years of environmental work experience,•Must have at least 2 years of air permitting & compliance experience, including direct technical work on at least one PSD/Title V air permit application.•Must have proficiency in Microsoft Office: Word, Excel, and PowerPoint.•Must have effective written and verbal communication skills.•Must have knowledge and understanding of local, state, and federal air quality regulations (Texas experience preferred).•Ability to work independently as well as in a team environment, strict attention to detail.•Excellent time management skills to manage multiple activities on an on-going basis within provided deadlines.•Must be authorized to work in the United States.•Preference will be given to candidates with Air Quality experience in Oil and Gas Upstream and Midstream operations.
Air Quality Specialist (Chemical/Environmental engineer)
Details: The Shaw Group provides premier engineering, design, construction, and maintenance services to government and private-sector clients in a wide array of industries, including the energy, environmental, infrastructure, and emergency response markets.Summary:The candidate would be expected to assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients. The candidate would be required to stay current on air quality regulations. This position is in Shaw?s Environmental and Infrastructure division, air quality consulting group. The hired person will work closely with mangers at their office location and Shaw?s National Practice Leader for Air Quality Consulting.Responsibilities:•The candidate will assist in preparation of proposals, conduct technical and regulatory analysis of emission sources, and prepare reports and present solutions to clients.•The candidate will be required to stay current on air quality regulations.•Work activities will include developing emission calculations (criteria pollutants, hazardous air pollutants and greenhouse gases), gathering technical data from clients and through independent research, determining regulatory requirements (e.g. NSPS, NESHAP, and NSR/PSD) for emission sources, and assisting in preparing compliance and permitting documents.•Additional responsibilities will include calculating emissions to determine health risk impacts using various emission models and documenting the results in a technical report.• Candidate may be located at client sites for extended period of time•Candidate will work closely with Project Managers in implementing project tasks.•Candidate must be flexible and willing to support other non-air related projects as needed.Qualifications/Competencies/Experience:•The required/minimum qualifications MUST be demonstrated/documented on the resume submitted to Shaw.•Must have BS degree in chemical, petroleum, environmental, or mechanical engineering and 3 years of environmental work experience,•Must have at least 2 years of air permitting & compliance experience, including direct technical work on at least one PSD/Title V air permit application.•Must have proficiency in Microsoft Office: Word, Excel, and PowerPoint.•Must have effective written and verbal communication skills.•Must have knowledge and understanding of local, state, and federal air quality regulations (Texas experience preferred).•Ability to work independently as well as in a team environment, strict attention to detail.•Excellent time management skills to manage multiple activities on an on-going basis within provided deadlines.•Must be authorized to work in the United States.•Preference will be given to candidates with Air Quality experience in Oil and Gas Upstream and Midstream operations.
Metrology Engineer
Details: Primestaff has a fantastic direct hire opportunity for a Metrology Engineer in Minneapolis, MN. The candidate hired will have between 3-5 years of experience who will grow into the role. This person will be working more with front end R&D and development engineering in developing new test procedures and calibration techniques as well as testing designs and new products being developed by the engineering group. Will also be responsible for documenting the developed procedures and training other engineers and technicians. Some of the job duties and responsibilities for the position include:- Work with Engineering and R&D teams to define and conduct appropriate DVT testing for electromechanical components and systems.- Proactively develop new procedures and equipment for calibration of new and existing products.- Maintain/Create documentation for testing & calibration process methodology of all released products and integrate these into the Quality Control (QC) and Quality Assurance (QA) functions.- Analysis of calibration data to investigate long term trends in instrumentation performance and accuracy, as well as provide process control feedback to the Manufacturing department.
Friday, 20 July 2012
Biomedical Technician I - Kokomo, IN
Details: DescriptionMaintain technology—and the highest level of patient confidence. Ensure the best possible outcomes with the best possible solutions. Help others to feel better in every way. Connect with your goals and change lives with Fresenius Medical Care North America. Use your professional skills and personal touch to create strong, lasting connections with our uniquely committed team. As the global leader in dialysis healthcare, we listen and respond to the needs of our patients and their families. While building the relationships essential to a positive healthcare experience, we establish careers that bring unique rewards. Why Join the Fresenius Team? Passion. Dedication. Knowledge. Motivation. Experience. These are the impressive qualities you’ll find in the Fresenius Leadership Team. Our strength in the North American market and extensive global network provide our employees with the best of both worlds—the friendliness of a local organization and the stability of a worldwide organization—for diverse experiences and challenging career opportunities. When you join the Fresenius Medical Care team, you’ll be welcomed into a company that is built on the philosophy that our employees are our most important asset. Our career advantages include the following: Fresenius Medical Care is the nation’s largest provider of renal care, meeting the needs of more than 135,000 patients at 1,800 clinics throughout the country. Our well-established, trusted organization fosters a spirit of camaraderie, emphasizing friendly collaboration, professional support, and career development. Superior training, UltraCare® quality control, and certification procedures ensure your potential to succeed and advance as a professional. Competitive compensation and exceptional benefits. Outstanding tuition reimbursement program. Recognized among Fortune’s “World’s Most Admired Companies” in 2011. National Safety Award from CNA insurance companies for 11 consecutive years. Opportunities to give back by participating in philanthropy and community outreach programs. Biomedical Technician I Here is an outstanding opportunity to play an important role with a major healthcare organization. As a part of our Centralized Technical Program team, the professional we select will manage the operational condition, maintenance, and repair of water systems, medical equipment, and mechanical/electrical systems. In addition, this individual will document repairs, perform safety checks and preventive measures, and conduct patient tours to explain the role our technology plays in their treatment. PURPOSE AND SCOPE: Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. Under supervision is responsible for the operational condition, maintenance, and repair of all water systems, medical equipment, and mechanical/electrical systems in assigned facilities in the Centralized Technical Program so as to ensure the safety of the patients as well as the staff operating the equipment. Performs all repair and maintenance activities according to company and department standard operating procedures and in compliance with local, state and federal regulatory requirements. Responsible for cost containment with regard to equipment maintenance and repair. DUTIES / ACTIVITIES: CUSTOMER SERVICE: Responsible for driving the FMS culture through values and customer service standards. Accountable for outstanding customer service to all external and internal customers. Develops and maintains effective relationships through effective and timely communication. Takes initiative and action to respond, resolve and follow up regarding customer service issues with all customers in a timely manner. PRINCIPAL RESPONSIBILITIES AND DUTIES Ensure availability for patients’ questions and concerns, for example to explain the principles behind the technology used. Provide instructive tours of the water treatment equipment for patients and explain the basics of the machines Maintain and repair all water treatment equipment, dialysis equipment, medical equipment, testing equipment, and mechanical/electrical systems as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the Technical Policies and Standards manual. Document all equipment and system maintenance and repairs. Ensure safety checks and routine tasks are conducted and documented in a timely fashion according to the established policies and procedures. Perform all facility preventative maintenance on machines, equipment, and systems according to standard procedures. Responsible for equipment cleaning and disinfecting according to specified standards after repair and maintenance has been performed. Ensure all testing equipment is properly maintained and calibrated. Evaluate the current equipment inventory. Actively support the CQI process. Adopt quality accountability. Participate in quality training and education for all technical staff. Participate in the completion and documentation of ongoing technical CQI activities as appropriate. Update and provide management with feedback regarding any improvement strategies that may be implemented. Assist with updating chemical inventory list Cooperate with facility staff to ensure all regulatory and OSHA requirements are met. Collect water samples for AAMI analysis according to company, state, and federal regulations and document as appropriate. Notify the appropriate personnel if results are outside the required/standard parameters. Assist in the review and updating of the alternative water supply plan. Coordinate with the appropriate vendors to ensure all dialysate and electrical leakage meters are calibrated as required. Assist in ensuring that all inspections by outside vendors are performed as needed. Ensure water and dialysate samples are processed according to specified procedures. Ensure all areas are safe - that environmental integrity and aesthetics are maintained. Transport equipment and supplies as needed. Other duties as assigned.
2012-1496 Laboratory QA/QC Program Manager
Details: Overview:Under the direction of the Manager of Laboratory Services, the Water Quality QA/QC Program Manager administers and maintains the Quality Assurance Program of the Company’s Drinking Water Laboratory, in full compliance with the California Code of Regulations; evaluates, reviews and approves the monitoring and analyses of laboratory test results to ensure methods used are in compliance with all environmental monitoring programs and regulatory requirements; conducts and documents independent and continuous audits of laboratory practices and procedures in conformance with all pertinent US Environmental Protection Agency (EPA), and the California Department of Public Health’s (DPH) Environmental Laboratory Accreditation Program (ELAP) certification specifications. This position is located at General Office in San Jose, California.Responsibilities: Monitors, evaluates, reviews and approves laboratory’s test results to ensure all data reported meets the minimum acceptance criteria for pertinent regulatory compliance monitoring. Technically oversees the work completed by Senior Chemists, Chemists, Senior Microbiologists, Microbiologists and Technicians. Makes recommendations for the approval of all Company contract laboratories. Oversees, coordinates, approves, or rejects work based on QA/QC requirements performed at Company contract laboratories. Develops, administers, monitors, evaluates, and maintains the laboratory’s EPA and ELAP mandated Quality Assurance Program to ensure the laboratory operates in conformance with the ELAP standards. Writes or oversees and controls the updating of all Standard Operating Procedures and QA Manuals. Oversees all Proficiency Testing and Method Detection Level studies. Develops and implements QA training programs in both the laboratory and in the District. Implements and maintains corrective action programs. Utilizes specialized software (LIMS). Performs independent assessments or special projects relating to the technical aspects of the laboratory/data and relating to State/Federal proposed regulations or implemented regulations. May provide leadership, guidance and/or technical support to laboratory staff. May perform certain additional duties as assigned by the Manager of Laboratory Services to facilitate the smooth operations of the laboratory in his/her absence. Attends relevant seminars, conferences and training as related to water quality issues; represents the Company during meetings with other departments and regulatory agencies. Participates in and supports the Company’s Continuous Improvement approach to business. Performs other duties of a similar nature or level.
QC Validation Chemist
Details: QC Validation Chemist - Vista / San Diego CA area Salary - BOE Kelly Scientific Resources is seeking an experienced Quality Control (QC) Validation Chemist for a dynamic chemical company in the San Diego North County coastal area. The qualified QC Validation Chemist will be responsible for a wide range of QC analytical release methods HPLC, chromatography, etc . The selected candidate will be familiar with validation concepts, GMP, and will have good protocol and report writing skills. The qualified individual will be able to work in a fast pace environment, being able to work independently and within the group. The qualified Validation Chemist will possess the following: 2+ year relevant experience in QC analytical release methods Strong knowledge of HPLC Experience in a GMP setting Here is the general information/job description. 1. Perform QC analysis to include: HPLC, Water content, Mass Spec, UPLC, UV, GC, GC Headspace, melting point, Optical Rotation, TLC and misc wet chemistry lab work. This work may include calibration and validation of these methods. 2. Develop the analytical methods and write the analytical method development report. Write standard operating procedures, standard test procedures and other related GMP documentation. 3. Write the validation protocols, execute the protocol and write the validation reports. 4. Execute validations as necessary to include QC Analytical methods performed, other validations to support the quality of the manufacturing facility. A college level degree bachelors or masters in a scientific field with equivalent experience of a minimum five years in GMP industry. Kelly Scientific Resources® (KSR) is the world's largest provider of staffing and HR solutions services to the biotechnology and pharmaceutical industry. By consistently providing key personnel in the areas of bioinformatics, combinatorial chemistry, genomics, clinical research and R&D, KSR has earned the reputation of being a quality, innovative staffing provider. KSR is a unit of Kelly Services, Inc., a Fortune 500 company and a global staffing industry leader for over 60 years.
Wednesday, 18 July 2012
Synthetic Chemist
Details: Kelly Services is in need of a Synthetic Chemist to join the team at an Industry Leader in Electronic Materials located in Marlborough, MA. Candidates must have a BS with 3-5 years of industry organic synthesis experience OR MS/PhD degree with 1-3 years of industry organice synthesis experience. Synthetic Chemist:• Synthesize novel organic/organometallic small molecules/polymers used for electronic materials in semiconductor industry.• Assist in development of practical and robust methodologies for synthesis and isolation of critical raw materials which will target general utility, high manufacturing precision, and ease of transfer to larger scale operations on site or at a vendor.• Collect preliminary process and characterization data for synthesized materials, and post regularly in a shared database to document and publicize results.• Maintain detailed experimental batch records to record observations, enable accurate replication of prior work, and provide a basis for establishing process control parameters• Communicate observations, impressions, and suggestions about existing or proposed chemical processes to the team leader.• Interface with R&D material synthesis teams and formulation teams to develop new materials• Establish and maintain a safe laboratory working environment, both in the personal zone of operation and as a member of the immediate laboratory community Qualifications• BS degree with 3-5 years of experience in organic synthesis, MS or Ph.D. degree with 1-3 years of experience in organic synthesis• Experience in organometallic chemistry is a plus.• Experience in polymer synthesis, modification, and characterizations• Hands-on experience in analytical equipments such as NMR (1H, 13C) spectroscopy, GC-MS, LC-MS, and column chromatography• Fluency in standard software applications (Word, Excel, Powerpoint, ChemDraw)• Proven track record of problem solving skills• Effective communication and interpersonal skills • Working effectively both individually and in a diverse, multi-disciplinary research team environment• Experience in photolithography industry is a plus Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position, you must use ???the apply??? now button below to submit your resumes. If you have questions about the position, you may contact the recruiter recruiting for this position, Rachel Pratt, email RACP, please submit your resume to RACP .
Research Associate
Details: Position Objective:The Research Associate will support the lead clinical molecule, C16G2, by conducting in vitro microbiological studies. The Research Associate will be working in a single laboratory under the direction of the Lead Project Scientist. This is a great opportunity for recent graduates considering a career in biotechnology or the life sciences.Responsibilities: Carry out biochemical assays under supervision of project scientists Grow cultures of oral bacteria, including pathogenic strains Work with antimicrobial peptides Work with biofilms and mixed bacterial cultures Conduct semi-high throughput screening and fluorescence microscopy Maintain laboratory notebook and accurate records of daily experiments Process, analyze and organize large data sets Prepare media, and stock solutions Assist in general upkeep of laboratory and maintain a clean work environment Other duties as assigned Working Conditions: This is a full-time position for work in a laboratory environment that maintains standard weekday operating hours of 8 am to 5 pm. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Little to no travel is required of this position. Employment Compensation: Position is salaried. Pay is competitive and commensurate to skill set and experience. Benefits include medical & dental Insurance, vacation plan, and 401(k). Consideration for future stock option grants may be available.
Lab Support & Rework Tech
Details: Candidate will be responsible for technical functions in support of engineering activities in validation labs. Must have experience with board assembly / rework, oscilloscopes, Logic Analyzers, voltage meters and soldering. May perform initial root cause of the issues encountered during the testing (hardware & software). Able to do multiple reworks in short time on several systems. Maintain online tool to reflect the status of rework. Coordinate reworks with HW Team and system integration lead. Support board debugging quickly. Support inventory tool during crunch times to inventory HW quickly and ensure proper distribution of HW within 24 hrs of HW being tagged. Some purchasing assistant or inventory management work may also be included in the position.
Full-Time Pharmacy Technician I - Waynesville
Details: PharMerica Corporation is a premier institutional pharmacy services provider, dedicated to providing quality patient care and innovative pharmacy solutions to institutional customers and patients in long-term care settings. With nearly $2 billion in annual revenues, PharMerica is the second largest institutional pharmacy company in America. PharMerica operates more than 100 institutional pharmacies in over 40 states and serves nursing facilities that care for approximately 350,000 patients.PharMerica Waynesville is recruiting a Full-Time Pharmacy Technician I to join our team.Essential Functions:Assists the Pharmacist in filling prescription items, as permitted by the State Board of Pharmacy.Types prescription information to produce labels.Labels products appropriately, including cautionary or auxiliary labels.Takes inventory, places orders, checks in drugs and supplies, stocks shelves and removes out-of-date items from the inventory.Inputs patient data and medication orders into a computer system.Prepares medications including emulsions, liquids, powders and ointments.Packages medications for dispensing and for delivery.Sanitizes IV room, equipment and hood.Communicates with nursing center personnel and other customers in a pleasant and professional manner.Processes returned medications from the facility for credit or destruction.Knowledge of Data Entry and / or IV experience is a plus.Minimum Qualifications:High School Diploma or equivalent.Certification if required by state.Minimum one year experience in a long-term care pharmacy preferred.Interested candidates please apply on-line @ www.pharmerica.com
Vascular Technologist
Details: The Barnabas Health Breast and Family Imaging Center, located in Bedminster, NJ is affilitated with the Barnabas Health Ambulatory Care Center in Livingston, NJ. The Center provides the highest quality medical care in an environment designed to set a new standard for patient satisfaction. We have combined the exceptional Saint Barnabas Medical Center medical staff with state of the art technology and put them within your reach today. Will perform all necessary test protocals on vascular patients. Must have current vascular certification. Previous experience is required.EOE
Chemist Job
Details: Department: Scientific Requisition Number: IE68957Interest Category: Environmental/SciencesInterest Sub Category: ScientificJob Title : ChemistEmployment Category/Status: full-timeType of Position: Regular HireCountry: U.S.State: NebraskaCity: OmahaMinimum Requirements: • Bachelor’s degree in chemistry.• Working knowledge of instrumentation and laboratory methods.• Must be proficient in standard office computer applications and software, to include MS Word, Excel, and Access.• Position requires analytical and interpersonal skills, and solid planning and organizational skills.• Candidate must be able to work independently without direct supervision.• Candidate must have a valid driver's license.• Candidate must be able to travel occasionally as needed.Job Description: The position will be part of the URS Omaha, NE office. This position will involve coordination of analytical and QA/QC tasks associated with environmental sampling and analysis (groundwater, soil gas, soil, indoor air) for environmental investigations and military munitions response projects. Perform sample collection, data review, field instrument analysis, and report production, including field work plans, sampling and analysis plans, and investigation reports.• Performs data review and validation for multi-media data.• Ensures project- and QAPP-specific data requirements are met.• Supports field efforts by preparing sampling plans, sampling matrices, bottle labels, and field documentation.• Works with data management to manage data flow from the laboratory to final reporting.• Researches environmental laboratory practices and methodologies.• Prepares proposals, procures and oversees laboratory services and approves invoices.• Conducts field and laboratory technical system audits.• Prepares technical reports and papers, and QAPPs.• Coordinates with end user to define data quality requirements and to help assure that data are scientifically sound and are usable in meeting end-use objectives.• The responsibilities of this position include, but are not limited to those stated above. For immediate consideration, please submit your resume online at www.urscorp.com and refer to Requisition # IE68957URS does not accept unsolicited resumes from third party agencies or recruiters. No fee will be paid to third parties who submit unsolicited candidates directly to hiring managers. All resumes must be submitted by the applicant to be considered for a position at URS.URSCB018EOE M/F/D/V
Nuclear Engineers w/ PE
Details: Job Classification: Direct Hire Aerotek is currently in need of multiple nuclear engineers looking for long-term employment in the Kansas City market. Our client is looking to grow their nuclear division and need quality engineers of all disciplines that could assist with developing their industry share, so connections with utilities/plants is a strong benefit. These opportunities will likely be direct hire, but exceptions will be made based on candidate needs. There is a need in all disciplines, but 10+ years of experience in the nuclear engineering industry would be preferred as well as a PE license. Very competitive salary and benefits will be offered.I look forward to reviewing your resume...Thank you!Join Aerotek Energy Services®, one of the largest providers of specialized personnel and management services to the commercial nuclear industry, the Department of Energy, the utilities industry, and engineering and consulting firms throughout North America. Assignments vary from several weeks to several years with many offering permanent opportunities. Aerotek offers comprehensive benefits to include medical, dental, optical, and optional 401k. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Energy Services team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.
Immunology Clinical Laboratory Scientist
Details: Immunology Clinical Laboratory ScientistGeneral Purpose of the Job:This position is responsible for troubleshooting, maintaining and performing laboratory assays for the detection and characterization of antibodies, antigens, cytokines, chemokines, complement components, identification of lymphocyte subsets, and evaluation of cellular immunity in clinical specimens. The position will be responsible for establishing and maintaining 8-color flow cytometry analysis and will play a significant role to ensure that assays are validated and performed in accordance with strict quality standards. The position will also support the Laboratory Manager to ensure that immunology results are generated in a timely manner to meet client expectations and that appropriate staff are trained to perform these assays.Reporting to: The position reports to the Laboratory ManagerPrimary Responsibilities: Provide technical guidance, training and problem solving on all immunology-based assays that are performed in the laboratory Perform day to day tasks to ensure that immunology assays are performing according to expectation and meet all quality standards. This includes ensuring and maintaining documentation that all instruments and reagents are operating according to specification Assist to develop and/or maintain quality standards that meet CAP requirements for accreditation of Immunology, Flow Cytometry, Histocompatibility, Transfusion Medicine, and other areas relevant to immunology testing as applicable. An essential task Participate in the day to day testing of specimens and working to ensure turn-around-times are met Create Standard Operating Procedures describing the appropriate technique for all immunology-based assays and assist Laboratory Manager in ensuring that all technologists performing the analysis have been fully trained with appropriate documentation Under the direction of the Laboratory Manager, develop and validate new immunology-based assays as required by clients Introduce commercially available assays and instrumentation in order to ensure that the laboratory is operating on current technology and platforms Work with lab management to ensure that the immunology functions within the lab are adequately resourced and equipped to meet the current and future needs of Eurofins Medinet Work with laboratory staff to ensure the timely purchase of all supplies and equipment for immunology-based testing to meet resource demands and cost control efforts Assist the laboratory in its endeavors to comply with the requirements of Good Clinical Practice (GCP), if required, the College of American Pathologists (CAP) and other relevant regulations. Ensure all QC requirements are performed and drive issue resolution within the laboratory As appropriate and as directed by the Laboratory Manager, work in other areas of the laboratory production including hematology, urinalysis and clinical chemistry Perform related duties as assigned
Laboratory Packaging Coordinator
Details: Adecco Medical & Science, a leading provider of contract and permanent staffing in the Pharmaceutical, Life Science Technology, Medical Device, and Health Care industry is seeking a Laboratory Packaging Coordinator on a temp-to-perm opportunity in North San Diego County. Responsibilities are as followed but not limited to:Follow approved GMP manufacture direction such as standard operation procedure, standard test procedure, master batch record and other procedures to handle packaging schedule, perform packaging the product and other related activities. Assist purification manager for monitoring material inventories for cleanroom use. Follow SOPs and approved direction to schedule cleanroom cleaning. Monitor compliance of manufacture and cleaning procedures of and equipments used in purification by periodically reviewing and signing off on maintenance and cleaning logs for each equipment. Schedule equipment calibration. Dispose chemical waste generated in the purification. Manage, order and negotiate material used in purification. Participate in problems solving in purification. Monitor and record cleaning room air-handling system performance. Requirements:BS in Chemistry from a 4-year university0-2 years of work experienceEntry-level candidates are encouraged to apply If you are interested in this opportunity or other opportunities available through http://www.adeccousa.com please apply online or email your resume directly to . The Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Medical and Science offers benefits including Tuition Reimbursement, 401(k), and Insurance Benefit Plans. Adecco Medical and Science is an Equal Opportunity Employer.
Stack Tester
Details: Weston Solutions, Inc. (WESTON®) has an exceptional opportunity in our Auburn office for a Stack Tester.Air Quality/Emissions testing. Employee will provide stack testing services to clients on-site.Will provide clients with accurate and pertinent scientific data according to agreed upon methods, procedures, and techniques. Provides sound conclusions and recommendations based upon field investigations and literature reviews within the established project.Position requires up to 75% travel.EOE, M/F/D/V. Smoke/drug-free workplace. Drug screening/ background checking employer. http://www.westonsolutions.com/careers/jobdescription.aspx?ID=3414
Chemist 3
Details: Weston Solutions, Inc. (WESTON®) has an exceptional opportunity in our Auburn office for a Chemist 3.Under the direction of the Section Manager/Unit Leader, provide clients with accurate and timely analytical data following established methods, analytical procedures and techniques, and proper quality control protocols. The work includes the preparation of reagents, usage of standard analytical glassware and instrumentation, calculation of results, review of work, and entry of data into laboratory information management system (LIMS).EOE, M/F/D/V. Smoke/drug-free workplace. Drug screening/ background checking employer. http://www.westonsolutions.com/careers/jobdescription.aspx?ID=3413
Pharmacy Technician - PRN - Clear Lake LTAC (Webster, TX)
Details: MUST BE IV CERTIFIED & STATE CERTIFIED. Essential Functions: Assists the Pharmacist in filling prescription items, as permitted by the State Board of Pharmacy. Types prescription information to produce labels. Labels products appropriately, including cautionary or auxiliary labels. Takes inventory, places orders, checks in drugs and supplies, stocks shelves and removes out-of-date items from the inventory. Inputs patient data and medication orders into a computer system. Prepares medications including emulsions, liquids, powders and ointments. Packages medications for dispensing and for delivery. Sanitizes IV room, equipment and hood. Communicates with all customers in a pleasant and professional manner. Processes returned medications from the facility for credit or destruction. Knowledge of Data Entry and / or IV experience is a plus.
Metrologist - 2nd Shift
Details: DescriptionThe Deeper End of the Talent Pool. Connect with the BEST custom contract manufacturers with primary emphasis in the state of the art precision machining and finishing of components used in aerospace to medical device manufacturing and all machining dominant industries in between!! MPS Technical specializes in the placement of contract and direct placement of staff that meet and exceed our client’s expectations. By focusing on quality of service and providing creative human resource solutions for our clients, MPS will continue to be the partner of choice for individual employees and our business clients. For the past 20 years, we’ve identified and partnered with those companies who best exemplify a strong commitment to smart business practices and recognize the importance of their professional employees! MPS Technical has partnered with a state of the art manufacturing company located in New Richmond, WI. We are actively recruiting for a Metrologist for a contract (3-6 months) opportunity with our client. To apply please see contact information below. Role: MetrologistLocation: New Richmond, WIShift: 2nd 3pm-11pmGeneral Summary: Provide necessary information needed to verify that tooling and parts meet or exceed customer requirements. Actively involved in the AQP process.Duties: Organize and complete First Article layouts and Capability Studies Ability to operator and set up CMM’s Maintain laboratory systems, procedures, and policies to meet or exceed customer requirements May perform color studies, submission packages, geometric design and tolerance Participate in Advance Quality Planning; which may include Gage R&R, FMEAs, and flow diagrams Perform MSA analysis and provide interpretation to engineering Verify compliance to engineering specifications Compile necessary paperwork, SPC charts, raw material certs, and paint lab reports to complete certifications sent to the customer Perform raw materials testing, update SPC data, file and update color chips. File all necessary certifications, reports, etc May provide guidance to measurement personnel Select, program and operate all measurement systems; able to run all software Identifies the appropriate measurement method
Associate Stack Tester
Details: Weston Solutions, Inc. (WESTON®) has an exceptional opportunity in our Auburn office for an Associate Stack Tester.Air Quality/Emissions Testing. Employee will provide stack testing services to clients on-site.Will provide clients with accurate and pertinent scientific data according to agreed upon methods, procedures, and techniques. Provides sound conclusions and recommendations based upon field investigations and literature reviews within the established projects.Position requires up to 75% travel.EOE, M/F/D/V. Smoke/drug-free workplace. Drug screening/ background checking employer. http://www.westonsolutions.com/careers/jobdescription.aspx?ID=3415
Cell Site Deployment Manager
Details: Job Description:Managing on cell site equipment deployment for UMTS and LTE equipment. Vendor management through installation and optimization services. Skill:Project Management Mobility Experience
Assistant CMC Project Manager
Details: Vertex Pharmaceuticals is seeking an Assistant CMC Project Manager to join our Pharmaceutical Development team in Cambridge, MA.The Assistant CMC Project Manager:- Performs a variety of well-defined support functions and may be responsible for limited independent initiatives. - Works with supervisor in setting the objectives of these initiatives. - Applies project management knowledge and attention to detail skills in “troubleshooting”. The Assistant CMC Project Manager may be responsible for one or more specific Group/Department service functions.KEY RESPONSIBILITIES:- Under direction of supervisor, participates in limited areas of development projects and/or timelines, which vary in function and in scope - Performs administrative functions for the larger CMC Project Management team- Support project management systems cross-project including portfolio pages, general timelines and CMO/CRO metrics- Multi-tasks to effectively manage his/her efforts on multiple projects- Troubleshoots routine problems- Tracks materials needed for project execution- Takes meeting minutes and updates portals- Assists CMC Project Managers and working teams/suppliers in the execution of campaigns- Assists with drug substance or materials plan- Performs other duties as assigned
Sterile Processing Technician-Full Time-Afternoon Shift with Rot
Details: Decontaminates, inspects and assembles surgical trays. Operates sterilizers. Distributes sterile supplies and equipment for use in patient care areas of the hospital. Full time position working primarily on the afternoon (2 pm-10:30 pm or 3 pm-11:30 pm) shift including rotating weekends (Saturday and Sunday) and rotating holidays. Must be available to rotate to other shifts on an as needed basis (7 am-3 pm, 10:30 pm-7 am and 11 pm-7:30 am).
Director Small Cell Operations
Details: Position Summary Provides key leadership in the development and adherence to small cell operational standards and practices with the ultimate goal of maximizing service availability and efficiently meeting customer service level agreements. This will be achieved through the staffing of a technical support team who will support the business in technical operational knowledge of small cells, provide clarity around impacts of common alarms, and provide rules and tools to help technicians drive speedy resolution to outages. The Director of Small Cell Operations will also have responsibilities for setting and ensuring adherence to operational standards by providing reporting, analysis, and physical audits to how work is performed. Essential Job Functions Lead Technical Support Group with responsibilities for Small Cell second tier support on active trouble tickets. Lead efforts on developing triage procedures for common alarms, developing and driving resolution to key operational issues with manufacturers, supporting special customer requests for new features/capabilities, alarm catalog and alarm severity templates for the fault management system. Ensure new system releases are implemented with minimal service interruption, providing leadership during incidents and creating post mortem reports, and generally driving constant improvement in system availability. Lead Quality assurance team with responsibilities for establishing operations standards for Small Cell installations, routine inspections, and preventative maintenance activity. Perform auditing the many teams within A&O, Implementation, and RF engineering to ensure adherence to our stated objectives. Lead the Service management team with responsibilities for owning the translation of customer SLA’s into active reporting, analyzing/mining data for alarms and outages, and providing recommendations for improvements (i.e. with our practices, equipment performance, vendor/contractor performance, etc.). Education/Certifications Bachelor’s Degree in Engineering or Information Systems Master's Degree preferred Experience/Minimum Requirements Minimum of ten (10) years in Operations or Engineering working for a wireless communications company Five (5) years management experience at the Sr Manager and/or Director level Experience in building new teams with technical focus Other Skills/Abilities Technical and operational knowledge of DAS, Wifi, and IT systems Technical and operational knowledge of some subset of the various cellular voice and data technologies (i.e. CDMA, GSM, WiMax, LTE, etc.) Demonstrated leadership and communication skills are required Ability to influence others Strong problem solving skills Ability to build effective cross-functional teamwork Organizational Relationship Reports to: Vice President of Engineering and Operations Title(s) of direct reports (if applicable): TBD Working Conditions: Works in a normal office setting with no exposure to adverse environmental conditions. Additional Information: N/A
Certified Pharmacy Technician - FT/Rotating
Details: Under the supervision and direction of the pharmacy director / staff pharmacist, fills routine orders for unit doses and prepackaged pharmaceuticals and performs related duties. Pharmacy technicians assist pharmacists in preparing and distributing medications, maintaining the drug inventory, and maintaining patient records. Pharmacy technicians work only under the supervision of a registered pharmacist, and do not perform duties that can legally be performed only by a registered pharmacist.
Senior Archaeologist Job
Details: Department: Archaeology Requisition Number: IE67531Interest Category: Environmental/SciencesInterest Sub Category: ArchaeologyJob Title : Senior ArchaeologistEmployment Category/Status: full-timeType of Position: Regular HireCountry: U.S.State: MarylandCity: GermantownMinimum Requirements: MA or MS in Anthropology or related field, completion of a university-based archaeological field school, and minimum of 6 years of archaeological experience; must meet Secretary of Interior (SOI) standards (36 CFR 61) in archaeology.The candidate will be well versed in standard archaeological field and analytical techniques for all phases of archaeological investigations as well as be able to design and implement new and improved techniques.The candidate must be prepared for field, lab, and office tasks, including data analysis and report writing and have experience in the supervision of junior staff to complete project assignments.Field projects could be located anywhere in the US and potentially overseas, and travel will be required. Valid Driver’s License required.Candidate will have demonstrated capability to write technical reports, and writing sample will be required.The Archaeologist should have the ability to perform bending, kneeling, standing, and lifting and carrying objects weighing 50 lbs and must have a tolerance for working in outdoor environments, including prolonged walking or standing on various terrain in a wide range of weather conditions.Job Description: Do the best work of your life!The Cultural Resources Group of URS is actively seeking a creative, highly talented Senior Archaeologist for immediate employment in the Germantown, Maryland office. The appropriately qualified applicant will be able to demonstrate an established career in Underwater and Nautical Archaeology. URS is proud to provide our employees with exciting, challenging projects.The Senior Archaeologist will provide support to cultural resource projects throughout the US and potentially international work, as available, and will have knowledge of Sections 106/110 of the National Historic Preservation Act and international regulations. They will have extensive knowledge of field excavation techniques and be able to successfully implement archaeological inventory, evaluation, and data recovery efforts, analyze prehistoric and historic artifacts, and prepare compliance reports as well as be able to design and implement new and improved techniques for projects.They will assist in the scoping of archaeological projects and utilize GIS, site records, and other data sources to identify locations where sites can occur. They will keep records and maintain the relevant State Historic Preservation Officer (SHPO) documentation pertaining to archaeological sites and architectural (built) resources. The Senior Archaeologist will provide regulatory compliance support for Federal, state, municipal, and/or commercial clients.The Senior Archaeologist will be able to serve as a Field Director and have experience in directing field crews under the guidance of the Principal Investigator. Must be able to mentor and guide junior staff in archaeological projects. This position supports all phases of archaeological investigation and regulatory compliance.This position may include manual labor including excavation with shovels and moving wheelbarrows filled with dirt.Geographic Information Systems (GIS), Global Positioning System (GPS), Total Station, Adobe Illustrator/Photoshop, Statistical Analysis (ex., SAS or SPSS), Register of Professional Archaeologists (RPA).Primary responsibilities:• Performs archaeological fieldwork, laboratory analysis, documentation, and interpretation focusing on the identification and evaluation of archaeological resources, writing determinations of eligibility and assessing effects on historic properties;• Leads crews and serves as Field Director under the direction of Principal Investigator, including scheduling work and making individual or team work assignments and leading the instruction of others in the use of equipment, technology, and field methods;• Communicates and coordinates with Historic Preservation Specialists regarding identified archaeological issues;• Coordinates with State agencies such as the SHPO and other interested parties regarding Section 106/110 consultation;• Coordinates with clients and International subcontractors or Governments regarding ESIA consultation• Reviews and writes archaeological reports and/or prepares archaeological site forms and coordinating with involved parties to assist in making decisions about project alternatives and the resolution of adverse effects to historic resources;• Collects information and makes judgments through observation, interviews, and the review of documents;• Coordinates with existing clients and potentially new clients;• Works with technical field, lab and office staff, managers and administrative staff to ensure that projects meet URS quality standards.Other duties as assigned.URS does not accept unsolicited resumes from third party agencies or recruiters. No fee will be paid to third parties who submit unsolicited candidates directly to hiring managers. All resumes must be submitted by the applicant to be considered for a position at URS.For immediate consideration, please submit your resume online at www.urscorp.com and refer to Requisition # IE67531.URSCB018EOE M/F/D/V
Quality Control Technician
Details: Kelly Scientific is actively looking for a outstanding QC Technician for a growing Pharmaceutical company in the Orange County area. Temp to hire 2nd Shift: 2-10:30pmSalary range: $13-15/hr DOEResponsibilities: Raw Material Release - Receive, collect and sample appropriate chemicals or components, and verify tests results for material release in accordance to raw material specification and applicable regulatory requirements or USP guidelines. When applicable, activities are to be performed in a controlled, clean room environment. - Perform physical testing of various components using measurement instrumentation/tools as required. - Provide support in the revision of Raw Material Specification and/or applicable controlled documentation including but not limited to Laboratory Test Submission (LTS) form and standard operating procedures - Support the routine cleaning activities of the controlled areas and supporting gowning area.In Process QC Support - Provide in-process QC support for the manufacture of all company Products. These activities may include, however are not limited to weighing, compounding, line clearance, visual inspection, label verification, scribing and/or other various QC activities as required. - Perform the QC testing on all sealable products according to all applicable standards. - Perform validation testing to support the release of raw materials, in-process materials and finished product. Execute protocols to support the validation of new equipment and products. - Any and all other duties assigned by immediate supervisor.Qualifications - High School Graduate with a minimum of three 93) years of experience in a pharmaceutical manufacturing environment. - AA in physical science (Chemistry, Biology, est.) or One to two years of academic classes completed towards a BS in physical science (Chemistry, Biology, est.) preferred - Strong word processing experience, spreadsheet and/or database desirable. - Document control (medical device documentation) Training in GMP/ISO preferred - Basic knowledge of software programs: Microsoft Word, Excel, FileMaker database, proofreading, attention to detail - Good oral and written communication skills - Strong organizational abilitiesInterested applicants should apply directly below to the on-line resume builder link. To follow up interested candidates may call us at 714-971-0721.
Lab Technician
Details: Lab Support is seeking Lab Technicians to work in QA, QC and R&D! Operate Analytical Equipment including HPLC, GC/MS, UV-Vis and FTIR to raw materials, in process and finished products Perform wet chemistry testing - pH, viscosity, density, moisture and concentration Follow FDA, SOP and company standards Draft and edit SOPs and Work Instructions Assist with method development and method validation projects Perform preventative maintenance and calibrations on equipment Troubleshoot lab equipment as needed
Assistant QA Laboratory Manager
Details: Our client, a large international manufacturing company, is currently expanding and offering excellent full-time career opportunities and a rewarding work environment. This industry leading company also offers competitive benefits, health insurance, bonuses, retirement plan, etc. Immediate career opening listed below. JOB DETAILS: Assistant QA Laboratory Manager$68,000 - $88,000 + bonus- Bachelor's Degree in Metallurgy, Chemistry, Materials Science or similar.- Requires experience with A2LA and ISO/IEC 17025 accreditation and compliance.- Plans, coordinates, and directs chemical laboratory activities and staff to assure accuracy of results.- Develops and implements laboratory standards, techniques, and technology.- Ensures laboratory is operating effectively and efficiently.- Daily management of laboratory operations. - Responsible for ongoing laboratory regulatory compliance including A2LA certification.- Work closely with suppliers and customers on development and testing.- Promotable to Sr Laboratory Manager role within two years.- Prefer 3+ years recent chemical lab or metallurgical lab experience in primary metals.- Confidential search, immediate opening. Date posted: July 18, 2012- All positions are direct hire, permanent placement.- All recruiting fees are 100% employer-paid.- Our placement services are free for all candidates.- Relocation assistance and benefits included. SEND RESUME TO: Pease email or mail your resume to:- David Smith - Sr Recruiter, The Career Source, LLC, P.O. Box 1885, Harrisonburg, VA 22801.- Email: Nationwide Recruitment since 1994:- Recruiting specialists for the Manufacturing Industry.- Engineering, Maintenance, Management, Operations, Quality.
Ph D Organometallic Chemist
Details: Job Classification: Direct Hire Established specialty chemical company in Somerset County, New Jersey looking for Ph D-level Organometallic Chemist. This research scientist role will require candidate to perform synthesis of organometallic compounds, designing and optimizing procedures for manufacturability.Serious Applicants OnlyJoin Aerotek Scientific®LLC, one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities. At Aerotek Scientific, we know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek Scientific offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Scientific team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.
Associate Director, Regulatory Medical Writing
Details: Overview:POSITION SUMMARY:Provides technical and editorial expertise and administrative guidance to medical writers within the Worldwide Clinical Research Department with regard to regulatory document preparation processes, standards, quality, and timeliness in support of drug development, product registrations, and product marketing. The incumbent creates, revises, and maintains document templates; manages and oversees document quality control; coordinates clinical quality assurance workflow; and edits and critically reviews regulatory documents. Depending on the structure of the group, the role may be mainly focused on the operational aspects of document preparation or on document review, editing, and writing.Responsibilities:ESSENTIAL AREAS OF RESPONSIBILITYProvides technical expertise to writers in the use of document templates and other tools for the preparation of regulatory documents to ensure adherence to relevant standards and applicable regulations and guidelines.Provides editorial expertise to writers in the preparation of high“‘quality regulatory documents to ensure both high editorial quality and adherence with agreed writing standards.Provides administrative guidance to writers to ensure that standard processes and accepted practices are followed with regard to developing schedules and the overall preparation of documents.Develops and maintains document templates and guidance documentation.Works with writers and quality control (QC) staff to schedule document QC according to agreed time lines, and manages the QC workload.Works with writers and Clinical Quality Assurance (CQA) to schedule document audits according to agreed time lines.Performs macroediting of documents for organization, content, structure, and tone, and to ensure documents are consistent within clinical programs, and microediting of documents for punctuation, grammar, sentences, paragraphs, and writing styles.Critically reviews regulatory documents for content for comprehension and to ensure inclusion of clear and consistent messages.Represents Regulatory Medical Writing on interdepartmental projects and initiatives within Cephalon.10. Prepares regulatory documents as a senior contributor.
Tuesday, 17 July 2012
RN / Registered Nurse / Travel Nurse
Details: Registered Nurse / RN / Travel NurseSpecialty: Acute, ER, OR, Med Surg, Telemetry, ICU/CCU, Labor/Delivery and multiple other specialtiesLicensed Registered Nurse If you’re looking for variety, flexibility, options and convenience – not to mention great healthcare jobs -- you’ve come to the right place. Working for Supplemental Health Care puts you in charge of your career. We work with you to find jobs that fit you; what kind of work schedule you need, what type of facility you want to work in, what specialty you want to focus on…and all of the things that are important to you.We have openings for 13 week travel nursing contracts nationwide, working a guaranteed 36 hours per week. These contracts pay anywhere between $1,000 - $1,600 per week after taxes depending on benefits package. We offer rates that are among the most competitive in the industry. We also offer a full range of benefits and perks, including: Customized health, dental and life insurance 401(k) savings program with company match and immediate vesting Industry leading appreciation program called Our Rewards that lets you earn great gifts Life-time payments for referrals on nurses and therapists And to make your life on the road easier, we provide a variety of support services, including: Relocation reimbursement Private housing Personalized assistance with all aspects of the move Licensing assistance
RN / Registered Nurse / Travel Nurse
Details: Registered Nurse / RN / Travel NurseSpecialty: Acute, ER, OR, Med Surg, Telemetry, ICU/CCU, Labor/Delivery and multiple other specialtiesLicensed Registered Nurse If you’re looking for variety, flexibility, options and convenience – not to mention great healthcare jobs -- you’ve come to the right place. Working for Supplemental Health Care puts you in charge of your career. We work with you to find jobs that fit you; what kind of work schedule you need, what type of facility you want to work in, what specialty you want to focus on…and all of the things that are important to you.We have openings for 13 week travel nursing contracts nationwide, working a guaranteed 36 hours per week. These contracts pay anywhere between $1,000 - $1,600 per week after taxes depending on benefits package. We offer rates that are among the most competitive in the industry. We also offer a full range of benefits and perks, including: Customized health, dental and life insurance 401(k) savings program with company match and immediate vesting Industry leading appreciation program called Our Rewards that lets you earn great gifts Life-time payments for referrals on nurses and therapists And to make your life on the road easier, we provide a variety of support services, including: Relocation reimbursement Private housing Personalized assistance with all aspects of the move Licensing assistance
Medical Technologist (Microbiology) - PRN
Details: Position Summary:Responsible for competently performing moderate and high complexity testing. Analyzes, reviews and reports test results and quality control results andtakes remedial action when indicated. Ensures specimen integrity by adhering to the laboratory's procedures for specimen handling and processing.Adheres to departmental policies and procedures to include departmental programs, quality control, performance improvement and safety.
RN / Registered Nurse / Travel Nurse
Details: Registered Nurse / RN / Travel NurseSpecialty: Acute, ER, OR, Med Surg, Telemetry, ICU/CCU, Labor/Delivery and multiple other specialtiesLicensed Registered Nurse If you’re looking for variety, flexibility, options and convenience – not to mention great healthcare jobs -- you’ve come to the right place. Working for Supplemental Health Care puts you in charge of your career. We work with you to find jobs that fit you; what kind of work schedule you need, what type of facility you want to work in, what specialty you want to focus on…and all of the things that are important to you.We have openings for 13 week travel nursing contracts nationwide, working a guaranteed 36 hours per week. These contracts pay anywhere between $1,000 - $1,600 per week after taxes depending on benefits package. We offer rates that are among the most competitive in the industry. We also offer a full range of benefits and perks, including: Customized health, dental and life insurance 401(k) savings program with company match and immediate vesting Industry leading appreciation program called Our Rewards that lets you earn great gifts Life-time payments for referrals on nurses and therapists And to make your life on the road easier, we provide a variety of support services, including: Relocation reimbursement Private housing Personalized assistance with all aspects of the move Licensing assistance
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