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.
Showing posts with label ASSOCIATE. Show all posts
Showing posts with label ASSOCIATE. Show all posts
Wednesday, 18 July 2012
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
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.
Saturday, 14 July 2012
QC Associate
Details: Job Classification: Direct Hire Quality Control Technician 3Duties Work as part of a team that performs routine and non-routine analytical biochemical and molecular biology assays to support release, characterization and stability testing of raw materials, production intermediates and final goods.Job duties include but are not limited to:-Preparation, daily maintenance, and use of next-generation sequencing instruments and equipment.-Reordering, maintaining stocks and supply of QC lab reagents and consumables.-Careful documentation of lab procedures.Skills -Self starter, strong work ethic, strong organizational skills, strong communication skills, critical thinking, attention to detail and accuracy, the ability to work independently and in a team environment, are essential.-Flexible, able to respond quickly to shifting priorities and meet deadlines -Basic molecular biology laboratory skills such as pipetting, PCR, gel electrophoresis, etc. required. Experience with DNA or RNA sample preparation, sequencing, qPCR, and robotics is a plus.-Experience and familiarity with instrumentation a plus KeywordsEducation -High school diploma with 2 to 5 years of industry experience with Functional analysis QC of molecular-biology-based assays preferred, other QC, R&D or manufacturing experience will be considered.-Alternatively, a BS in Biology/Molecular Biology biochemistry, chemistry or related discipline with 0 to2 years of industry experience.-Ability to understand and follow work instructions and perform molecular biology assays with minimal guidance after initial training. -Proficiency with Microsoft Office tools (Excel, Word, and PowerPoint) -GMP experience a plusJoin 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.
Friday, 13 July 2012
Associate Research Fellow
Details: When you touch the lives of millions of people around the world, nothing but the best will do. That's why The Clorox Company and our subsidiaries look for people committed to work together toward common goals, while taking personal ownership for their decisions and actions. People who believe in maintaining the highest standards of business and professional conduct. People who share our values of strong competitiveness, measuring results and "doing the right thing." If you want to make your mark in millions of homes and do it where you can feel proud about it, apply now for this opportunity at Clorox. PRODUCT CONCEPT AND PROTOTYPE DEVELOPER Company Profile:The Clorox Company is a leading manufacturer and marketer of consumer products with fiscal year 2009 revenues of $5.5 billion. Clorox markets some of consumers' most trusted and recognized brand names, including its namesake bleach and cleaning products, Green Works® natural cleaners, Armor All® and STP® auto-care products, Fresh Step® and Scoop Away® cat litter, Kingsford® charcoal, Hidden Valley® and K C Masterpiece® dressings and sauces, Brita® water-filtration systems, Glad® bags, wraps and containers, and Burt's Bees® natural personal care products. With 8,300 employees worldwide, the company manufactures products in more than two dozen countries and markets them in more than 100 countries. Clorox is committed to making a positive difference in the communities where its employees work and live The Research and Development organization is at the heart of our business, taking new generations of consumer products from concept to reality. Over 90% of Clorox Products are #1 on the shelf, which means that we have great pride in delivering the best technology to the consumer every time. With such diverse roles as engineers, scientists, mechanical designers and packaging experts, R&D is a community of technical leaders and managers actively involved in virtually every step in the lifecycle of our products — from initial concept to raw materials to final goods on store shelves. R&D is committed to leveraging the latest technology to bring consumers the high-quality, innovative products they expect and deserve. Position Description:The Clorox Company has opportunities at our Research and Development center in Pleasanton, California for a scientist or engineer, with an advanced degree, to focus on product concept and prototype development. Working at the front end of innovation the role will focus on translating new concepts, ideas, solutions, benefits and technologies into protocepts and prototypes. Using iterative and incremental approaches the successful candidate will further develop these prototypes to enable business assessments, small scale consumer testing and manufacturability assessments. They will work cross-functionally with various discovery teams and interface their R&D work with the business and consumer elements of the project to ensure a holistic approach. They will reach out to both internal and external technical experts/suppliers to both identify and evolve their protocepts and prototypes and to build future capabilities. The successful candidate will need to have the ability to rapidly identify key ‘killer technical issues’ at each stage of a project, be able to integrate multiple work streams efficiently, and have the agility and focus necessary to move projects forward with only the essential required resources. The individual will need to have a broad as well as deep technical background and be to handle a diverse range of projects. Proven creative thinking and ability to work with limited data and direction is a must. Candidates will have a talent for analyzing problems from multiple points of view and connecting disparate ideas to create innovative solutions and concepts. Candidates must have a demonstrated ability to work in ambiguous situations, be proven self starters and be passionate and committed to world-class product and technology development. Qualified candidates will be technically advanced and highly motivated and be able to apply their skills to diverse, challenging problems in a fast-paced team environment. They must be comfortable contributing to projects that span a wide variety of consumer and professional product applications in a fast-paced business environment with rapidly changing needs and priorities. They will be expected to communicate and collaborate with colleagues in a variety of diverse disciplines and functions to deliver business-building solutions.
Wednesday, 11 July 2012
Associate Scientist II
Details: Under the direction and supervision of a GroceryCo Consumer Science manager, the Associate Scientist II (SG7) is responsible for the day- to-day sensory and consumer project management as well as sensory panel leadership activities for specified GroceryCo categories. Plans and conducts independent projects, participates in development of project objectives, executes against same, and recommends action plans to implement key findings Leads Sensory Panel; plans and conducts training to develop and maintain panel and provide sensory evaluation project support Has broad understanding of analytical work Begins to address increasing levels of complexity; capable of collecting information from different sources Consults with clients Develops basic understanding of Kraft Foods business
Tuesday, 3 July 2012
SR. QA COMPLIANCE ASSOCIATE
Details: SR. QA COMPLIANCE ASSOCIATEJOB PURPOSE: Support activities of the company’s document control system including the filing, changing and distributing of all current Good Manufacturing Practices (cGMP) electronic and paper copy documents in a manner that satisfies the requirements of our clients and corporate expectations. JOB RESPONSIBILITIES: Returned Good Authorization program Environmental monitoring program Discrepancies program Prepare and monitor Internal Audit program Prepare and monitor Supplier Audit program Corrective and Preventive Action (CAPA’s ) Program Calibration program Review and approval of Manufacturing Batch Records Review and approval of executed packaging batch records Review stability results Support maintaining document controls files and records, including records retention Support Packaging component inventory control Support Inspections of packaging and labelling components Support Finished Goods inventory control cGMP Training for employees Support preparation of annual product reviews in compliance with FDA and EU regulations Release of product and ensure accurate status of product Sign Certificates of Analysis and/or Certificates of Conformance On-Site Document Approval Monitor DI’s, LI’s, CAPA’s, Customer Complaints Documentation errors and Change Controls (provide trend analysis) Support activities with US and International Regulations in conjunction with Registration department Support for the East and West cost distribution centers Perform release and rejection of lots Monitor Pest Program May perform special projects as requested by the Quality Assurance and Regulatory Compliance Manager.
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