Quality Control Research Associate - I
Company: Planet Pharma
Location: Santa Monica
Posted on: January 13, 2022
Duties & Responsibilities
Under guidance and supervision perform Raw Materials release
testing by following well established procedures as written.
Maintains instruments, ensuring they are calibrated and ensure
proper routine maintenance is performed in a timely manner.
Author and revise, SOPs governing Raw Materials and supporting
activities such as solution preparation, aliquoting etc. as
Participate as needed in testing of raw materials by following
analytical methods: Compendial methods and or SOPs (pH, Osmolality,
Conductivity, LAL, Identity, ELISA, Gel/Western Blot, FT-IR,
Has previous experience and a solid understanding of the following
analytical methods: HPLC, Gel/Western Blot, and ELISA employing
GMP/GDP/GLP in practice with sufficient attention to detail.
Participate and own laboratory investigations, deviations, and
CAPAs related to raw materials, test methods, and OOS events, as
Support team members with other duties are required, such as
gathering documentation and data entry and routine lab upkeep and
Master's Degree and 2 + years' experience in the
Bachelor's Degree in Biology, Chemistry, Biochemistry, or S.T.E.M.
and 2+ years' experience in the biotech/biopharmaceutical or
Basic understanding and experience operating within an GMP
Exceptional attention to detail and ability to keep track of
multiple ongoing projects
Excellent oral and written communication skills
Ability to perform duties with minimal supervision and be adaptable
to a dynamic and fast-paced environment
Excellent interpersonal and organizational skills
The Planet Group of Companies is an equal opportunity employer. We
celebrate diversity and are committed to creating an inclusive
environment for all employees.
Keywords: Planet Pharma, Santa Monica , Quality Control Research Associate - I, Other , Santa Monica, California
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