🌙 QC Analyst – Night Shift | Bethlehem, PA
💰 $22–$24/hr. + 10% shift differential
🕒 7:00 PM – 7:30 AM | 2-2-3 schedule
📄 6-month contract
Join a FAST growing Pharmaceutical Manufacturing site supporting the production of Critical Care drug products in a GMP lab environment.
Job Summary: Perform analytical testing of In-Process, Bulk, Stability and Finished Product to provide information about the quality, identity, purity, and safety of the material and provide decisions into the next steps in the manufacturing process.
🔬 Key Responsibilities:
- Perform sample preparation and GMP testing of raw materials, in-process, bulk, stability, and finished product
- Operate and maintain analytical instruments (HPLC, GC, UV, FTIR, KF, ICP/MS, or AA)
- Complete GMP documentation in compliance with SOPs and data integrity requirements
- Support OOS, deviations, and lab investigations
- Prepare standards, solutions, and calibration activities
- Maintain lab logbooks, inventory, and stability samples
- Review analytical data and production records, including peer review
- Follow all GMP, safety, and quality procedures in a 12-hour shift environment
✅ Job Requirements:
- Must have at least 1 year of experience in a GMP laboratory setting.
- Familiar with GMP/GLP and FDA requirements a plus
- Strong documentation skills
- Familiar with SAP, OpenLab, Ensur, MS Office
