Overview:
This laboratory position will be in the Quality Control Department to support methods transfers and validations, as well as release and stability testing of large-molecule clinical and commercial projects. This position is based in Camarillo, CA.
Principal Responsibilities and Duties:
- Perform ELISA assays
- Be familiar with and perform wet-lab instrumentation and techniques such as protein concentration, appearance testing, pH, and osmolality
- Perform HPLC and CE analyses of proteins
- Perform method validations and verifications
- Perform method transfers
- Execute stability studies
- Maintain laboratory notebooks and appropriate documentation
- Author technical reports, protocols, presentations and memorandums
Requirements
Experience, Education, Training, Traits:
- BSc or MS degree in Biochemistry, Biology, Chemistry or other relevant discipline
- Minimum of 6 months of work experience in a GMP laboratory in the biopharmaceutical or pharmaceutical industry
- Experience with protein-based biopharmaceuticals
- Experience in performing cell-based bioassays and ELISA assays preferred
- Experience with HPLC and Capillary Electrophoresis assay for protein therapeutics highly desirable
- Strong attention to detail
- Familiarity with standard MS Word, Excel, graphics, and presentation software required
- Experience with electronic LIMS, e.g., Thermo Sample Manager, desirable
- Proven track record of productivity and problem solving skills
- High level of motivation, passion to learn, and adaptability to meet departmental objectives
- Excellent communication, interpersonal and organizational skills
Eurofins
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable.
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