Key Responsibilities:
- Typical test methods performed include, but are not limited to, flow cytometry, cell counting, cell culture, sterility (BACT), endotoxin (LAL), and Visual Inspection testing.
- Performs technical reviews of raw data.
- Records test results and maintain raw data and accurate laboratory records on paper and in electronic systems.
- Performs general lab and equipment maintenance duties.
- Performs other duties as assigned.
- Troubleshooting analytical methods and participating in Quality Events (Deviations, OOS)
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.
- Experience with electronic lab notebook (LIMS), and demonstrated ability to work with electronic instrument software
Requirements:
- A minimum of a Bachelor's degree in related field of science is required (Biology, Chemistry, Biochemistry, etc).
- 4-6 years of experience in the GMP pharmaceutical/biopharmaceutical industry
- Demonstrated laboratory experience in multiple methodologies listed above
Pay: $35.41 - $48.00 per hour
Application Question(s):
- Are you open for Third Shift?
9:30 PM to 8AM, Wednesday – Saturday
Work Location: In person
