Quality Control Analyst

Status: Accepting Candidates About the role 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. 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 Qualifications A minimum of a Bachelor's degree in related field of science is required (Biology, Chemistry, Biochemistry, etc). 2-6 years of experience in the GMP pharmaceutical/biopharmaceutical industry Demonstrated laboratory experience in multiple methodologies listed above Compensation (MA Pay Transparency): $40–$50/hr (W-2) Final rate within the posted range depends on qualifications and interview outcomes. #J-18808-Ljbffr