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Quality Control Analyst II

Company: Seqens North America
Location: Newburyport
Posted on: June 17, 2022

Job Description:

Job Description Position Context: Responsibilities: The analyst is responsible for providing accurate and timely results for the samples submitted for analysis to support our manufacturing and research and development departments. Main tasks: Perform routine analysis of Raw materials, In-process, finished products as well as stability samples and perform review of analytical test results by the direction of Lab supervisor. Perform calibration and maintenance of Lab equipment as required. Perform trouble shooting of equipment as required. Perform training of new analysts as per company training program. Understand the need to work on another shift in urgent situation. Perform lab cleanliness. Regular Duties: In addition to the above, other duties include but are not limited to: writing operating procedures for the laboratory. maintaining the chemical inventory. maintenance of the reference standard program. performing secondary data review for analyses conducted by other analysts. ensuring appropriate levels of laboratory supplies. Required skills: Requirements: B.S in science, preferably in Chemistry or Biochemistry or Biotechnology M.S preferred 2-to-3-year experience in laboratory environment. Experience in pharmaceutical Lab equipment, e.g.: HPLC, FTIR, GC, UV/Vis, KF and other standard equipment. Experience in GMP Lab environment. Company Description Seqens is an integrated billion-dollar global leader in pharmaceutical synthesis and specialty ingredients. Seqens CDMO North America (formerly known as PCI Synthesis, Inc.), a business unit of Seqens, is a Contract Development and Manufacturing Organization (CDMO) that provides biotech and pharmaceutical companies with the expertise and capacity needed to develop and manufacture complex small molecules including active pharmaceutical ingredients (APIs), intermediates and other specialty products, whether at research, development or commercial scale. The company also has extensive expertise in medical-grade polymer synthesis, flow chemistry, bio-catalysis and highly potent APIs. Seqens offers tailor-made solutions to sponsors for all their API needs. Seqens operates 24 manufacturing sites in Europe, North America and Asia and 7 R&D centers. In North America, Seqens CDMO operates a cGMP facility in Massachusetts, where its R&D and kilo labs are fully integrated with commercial manufacturing capabilities of up to 2000 gallons. Seqens offers competitive compensation and benefit packages. If you're dedicated and ambitious, Seqens is an excellent place to grow your career.

Keywords: Seqens North America, Lowell , Quality Control Analyst II, Professions , Newburyport, Massachusetts

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