DNAjobs.com is proud to feature the following jobs posted May 29 - June 5 (listed in chronological order). For each position, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason Skie
Biostatistician
(US-California-San Diego) Individual will work with project team to form statistical analysis plans, participate in data management activities as they relate to securing analyzable data, apply descriptive and inferential statistical techniques, and produce tables/listings via SAS for final clinical trial reports.
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Microbiology Assistant II
(US-California-San Diego) Provide assistance in the qualification of a new manufacturing facility. Will perform environmental monitoring, water and compressed gas testing, bacterial identification and other routine activities as needed.
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Part-Time Research Assistant
(US-California-San Diego) Part-time research assistant needed for performing quality control assays and general maintenance of a cell culture core facility. Duties include performing PCR ELISA for mycoplasma detection, preparation of cell culture media, routine laboratory maintenance and ordering reagents and supplies.
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Scientist
(India) If you have experience in fermentation technologies, protein chemistry, molecular biology, cell biology or sales or if you have recently graduated in one of these fields, we may have an opportunity for you.
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Scientist: Upstream Process Development
(UK) You will be work to optimise the current manufacturing process for recombinant poxvirus production. This will require varied cell culture experience; T-flasks, roller bottles, spinner flasks and bioreactors; complemented with experience in virology.
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Scientist: Downstream Process Development
(UK) Focussing on down-stream processing you will look at alternative methods for optimising and controlling each stage of the down-stream processing train. Familiarity with protein purifcation/characterisation and previous process development experience, ideally in a GMP background, would be an advantage.
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Analytical Development
(UK) Taking on in-house analytical testing of clinical trial material, you will implement, maintain, and work to GLP guidelines as required by the EU clinical directive, and in-house standards. Experience in working in a regulated environment (GMP/GLP) using molecular biology techniques will be a distinct advantage.
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Vivarium Research Associate
(US-California-San Diego) The ideal candidate will be well versed in GLP documentation for inlife studies and have at least 2 years of experience in the performance of testing procedures including injections and sample collections as required for rodent and rabbit studies being conducted.
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Vivarium Technician I
(US-California-San Diego) Primarily responsible for all aspects of rodent husbandry, maintenance of vivarium in accordance with regulatory requirements, inventory control, operation of vivarium equipment, and cage washing.
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Manufacturing Assistant I/II
(US-California-San Diego) Duties include preparing solutions in large scale (200L) in manufacturing plant; preparing equipment by washing, autoclaving, and depyrogenating, assisting with utility validation (water system sampling and testing air systems); and assisting with process validation.
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Director, Regulatory Affairs
(US-California-San Diego) This position is the principal tactical liaison with regulatory agencies and with internal functional departments and product development teams concerning specific domestic filings. The successful incumbent will provide leadership for subordinate regulatory functions involving IND filing and clinical/preclinical topics.
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Analytical Chemistry Associate Manager
(US-California-San Diego) The Analytical Chemistry Associate Manager will be responsible for leading a team of analytical chemists focused on the development of analytical methods used for the physical and chemical characterization of lipids, polymers, plasmid DNA, and process impurities in excipents, bulk drug substance and final product.
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Accountant I
(US-California-San Diego) Accountant needed to perform GL acct reconciliations, expense reports, government contract accounting, project cost accounting, and assist with corporate insurance renewal and A/P. B.S. Bus Admin/Acctg & knowledge of government contracts & grants preferred w/ 3-5 yrs general accounting experience required.
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Image Analysis Summer Internship (Graduate Degree Required)
(US-California-Telecommuting) Using specifications and background that will be provided to you, design (UML) and code image analysis in Java. A detailed specification will be provided to you upon completion of our NDA. You will be responsible for: Reporting your design specifications, issues and status reports to your Internship Manager.
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DNA Research Scientist
(US-Massachusetts-Boston) Seeking an enthusiastic, creative scientist with a strong working knowledge of standard molecular biology and techniques in DNA chemistry to work on the forefront of scientific discovery, interfacing nano- and bio- technologies while collaborating with academia and other independent laboratories internationally.
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DNA Laboratory Technician
(US-Massachusetts-Boston) Seeking an enthusiastic, creative scientific technician with a working knowledge of standard molecular biology to work on the forefront of scientific discovery, interfacing nano- and bio- technologies.
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Technical Sales Specialist
(US-New Jersey) Responsibilities include: Following-up leads and closing sales including applications assistance and after-sales customer support. Sales presentations for prospective customers. Generate quotations. User training, installation and customer support.
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Facilities Coordinator
(US-Maryland) This position reports to the Vice President of Operations. The individual in this position is responsible for implementing the Company's policies and procedures regarding the safeguarding and maintenance of its physical property, including buildings and grounds.
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GC & GCMS Marketing Specialist
(US-Maryland) This position reports to the Product Manager. This individual is responsible for the development of product positioning materials (i.e. writing of technical support materials, development of point of sales pieces, demonstration and presentation of products, market and competitive information gathering) for the product line(s).
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HPLC Service Engineer
(US) The individual in this position is responsible for a wide variety of service related support functions including, but not limited to, the repair, maintenance, and installation of HPLC and other assigned products.
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Senior Technical Specialist (HPLC)
(US) This position reports to the Product Manager for HPLC. This individual is responsible for the development of technical and product support documents related to marketing and sales of the HPLC product line. Significant travel and direct contact with accounts and market segments is required.
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Microbiologist
(US-Illinois-Chicago) Responsibilities for this key role fall into several main categories, including the following: Primary Activities Hygiene; Maintain NGMP Monitoring/Implementation ; HACCP Program & Monitoring; CIP Program & Systems; Identifies microorganisms by microscopic examination of physiological, morphological and culture characteristics.
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Biostatistician
(US-New Jersey) We currently have a need for a number of Biostatisticians for our client in New Jersey. Qualifications: - 2-3+ years clinical industry experience - Ph.D preferred but not required - Phase I experience preferred but not required - Pharmaceutical background (as opposed to CRO) strongly preferred.
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Product Specialist
(India) Should be a B.Tech (Textiles) with 5 to 7 years experience in textile chemical marketing. We believe that our people are our strength and in their growth we see our growth. Besides a good salary, we give handsome perks and benefits that include PPF, HRA, Medical, LTA, Bonus and Gratuity to right candidates.
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Senior Relational Database Developer
(US-California-San Francisco) We are looking for a Senior Relational Database Developer to design and develop new database schema to support medical image analysis for clinical trials. This is a highly regulated area and the qualified candidate should have effective database skills, have a methodical approach, and should thrive in a rapidly changing environment.
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Senior Medical Writer
(US-California-San Francisco) Responsible for writing, reviewing, editing and ensuring quality control of clinical study reports, clinical NDA sections and clinical sections of other regulatory submissions. Write clinical sections of Investigator Brochures Contribute to IND annual updates Write abstracts, posters and presentations for medical conferences along with manuscripts for medical journals.
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