Hiring 3 QC/Sr. QC Analysts _ Pharmaceutical Manufacturing
Must have HPLC and UPLC Experience in a GMP Environment. Seeking QC professional, however can considering strong Analytical Chemist in this space for one of the needs.
Job Details
• USP methods, where applicable. Supporting QC leadership with planning and coordination of activities within the lab.
• Physical testing, chemical, or microbiological analysis of raw materials, finished products, stability and special samples
• Documenting and submitting all raw data and results in LIMS
• Preparation of reagents for chemical analysis
• Microbiological media growth promotion
• Data auditing for lot disposition
• Method verification, validation and technology transfer for new products
• HPLC, UPLC, GC, ICP-MS analysis of raw materials, finished product, and stability samples
• Support QC Systems Admin activities (Empower, LIMS, Trackwise)
• Preparation and review validation/verification protocols
• Analyst training
• Leads laboratory OOS and OOT investigations
Required Experience:
• Needs someone with HPLC, UPLC experience (The software is Empower)
• Must have GMP experience
• Needs to be someone with high level experience (someone that has been doing this type of work for the past 5-7 years)
Seeking QC professional but open to high level analytical backgrounds as well • Specialization with HPLC, UPLC and GC systems
• Minimum 5-7 years’ experience in
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Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.