Shift: M-F, mostly 1st shift with some flexibility to work 2nd shift as needed
Pay: $31-33.65/HR, based on experience
Qualifications:
Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 5 years of experience in a pharmaceutical/biotech QC laboratory.
Previous experience in a cGMP laboratory environment.
Strong background in protein chemistry and experience troubleshooting analytical results.
Demonstrated success in writing, revising, and complying with SOPs, protocols/reports, and QC method
Expertise in techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, ELISA, and standard compendial assays.
Responsibilities:
Perform analytical testing to support product in-process, release, and stability programs.
Apply strong knowledge of cGMP, Quality Systems, and ICH/regulatory guidance in daily operations.
Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative action plans.
Work with cross-functional teams to advance projects, maintain equipment, and author documents and reports.
Train other analysts to perform laboratory procedures and assays.
Participate in internal assessments and audits as required.
Ensure compliance with all company policies and standards.
Perform additional duties as assigned.
This position is offered on a contract to hire basis, with permanent employment offered upon completing an initial 6 month contract.