2nd shift Quality Control Specialist/Sr. Specialist (Contract)

The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation, testing and reporting of in-process, release and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.

Key Responsibilities:

• Typical test methods performed include flow cytometry, qPCR (MycoTOOL), ELISA, cell counts, sterility (BACT), Gram stain and endotoxin (LAL) testing.
• Performs technical reviews of raw data.
• Records test results and maintains raw data and accurate laboratory records.
• Performs general lab and equipment maintenance duties.
• Performs other duties as assigned.
• Weekend shift work: Typical workweek is a 4 day week, 10 hours a day, Sunday to Wednesday 12:30 PM – 11:00 PM.

Knowledge and Skills:

• Performs tasks with strict adherence to cGMP and cGDP principles.
• Has an understanding of basic laboratory equipment and practices.
• Is proficient in the use of spreadsheets and word processing software.
• Is dependable and able to work well within a team.
• Is interested in learning new things. Open to change.
• Is optimistic and displays a positive attitude even during periods of adversity.
• Shows initiative; acts independently with management approval.
• Possesses a high attention to detail.

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Requirements

• A minimum of a Bachelor's degree in Sciences is required.

• 2-4 years (4+ for Sr.) of experience in the GMP pharmaceutical/biopharmaceutical industry

Benefits

• Training maybe 1st or 2nd shift - dependent on training schedule and assay
• 2nd shift – Sun-Wed 12:30pm-11pm