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QC Analyst III at Kashiv BioSciences, LLC

Piscataway, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Oct, 26

Salary

103000.0

Posted On

14 Jul, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, UPLC, Impurity Testing, Bio-assays, GMP Compliance, Technical Writing, Validation Protocols, Change Control Process, Analytical Support, Formulation Development

Industry

Pharmaceutical Manufacturing

Description

Description QC Analyst III (Piscataway, NJ): Be primarily responsible for the execution and review of HPLC/UPLC assays & impurity testing along with Bio-assays for release & stability purposes in a GMP-complaint Quality Control laboratory; independently write experiment summaries, laboratory investigations, technical reports, operation and test method procedure documents, and review documents comprising, but not limited standard operating procedures, standard test methods, validation protocols and reports. Salary: $103,000 per year. Requirements Req’s Master’s degree (or foreign equivalent degree) in Chemistry, Analytical Chemistry, or related, with knowledge of the following skills: preparing validation protocols and reports; preparing test methods and procedures; reviewing and approving CCRs according to the change control process; as well as providing analytical support for formulation development. Apply to HR at Kashiv BioSciences LLC, 20 New England Avenue, Piscataway, NJ 08854.

Responsibilities

Responsible for executing and reviewing HPLC/UPLC assays, impurity testing, and bio-assays for release and stability in a GMP laboratory. The role involves writing experiment summaries, technical reports, and reviewing standard operating procedures and validation protocols.