Role OverviewThe Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation.
What You Will Do
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. Support weekend lab operations and maintain training records. Assist in lab equipment and inventory maintenance, including reagent and sample prep.
Why It Might Be a Fit
B.S. in chemistry, biology, biochemistry, or related field. 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent. Experience in method transfer/implementation; understanding of method lifecycle management. Strong technical writing, data analysis, problem-solving, and organizational skills.
Requirements
- B.S. in chemistry, biology, biochemistry, or related field
- 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent
- Experience in method transfer/implementation
- Understanding of method lifecycle management
- Strong technical writing, data analysis, problem-solving, and organizational skills
Benefits
- Contract position with possible extension
- Weekend coverage is required
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