QA Senior Engineer - Inspection, Labeling, Packaging

This is a unique opportunity to join INCOG Bio Pharma’s Quality Assurance team in a highly visible role that directly supports the delivery of safe, effective parenteral drug products to patients worldwide. Reporting to the QA Director of Quality Systems, you will be part of a collaborative, fast‑paced environment where your expertise in inspection, labeling, packaging, and serialization quality systems will shape the future of our CDMO operations.

If you thrive in a culture of innovation and continuous improvement, this is the role for you.

The QA Senior Engineer of Inspection, Labeling, and Packaging is responsible for the oversight and continuous improvement of quality systems governing finished product inspection of aseptically filled vials, syringes, and cartridges, as well as labeling, packaging, and serialization operations. This role ensures that all associated quality systems are designed, implemented, and maintained in a state of regulatory compliance with FDA, EMA, and other applicable regulatory requirements.

The QA Senior Engineer serves as a subject matter expert (SME) and key quality partner to Manufacturing, Technical Services, Engineering, and Supply Chain teams to drive operational excellence and inspection readiness across all inspection, labeling, and packaging activities.

• Provide quality oversight and SME support for finished product visual inspection operations, including manual, semi‑automated, and automated inspection of filled vials, syringes, and cartridges
• Own and manage quality systems related to labeling, packaging, and serialization, ensuring compliance with FDA and EMA regulations; USP/ISO/ICH/PDA/ISPE and other non‑governmental guidance documents, and applicable serialization regulations (e.g., DSCSA)
• Author, review, and approve SOPs, work instructions, batch record sections, and specifications related to inspection, labeling, packaging, and serialization processes
• Lead or support deviation investigations, root cause analyses, and CAPA activities related to inspection defects, labeling errors, packaging failures, and serialization events
• Collaborate with Manufacturing, Engineering, and Technical Services to develop and qualify inspection parameters, AQL criteria, and defect libraries for new and existing products
• Ensure inspection, labeling, and packaging quality systems maintain audit and inspection readiness for FDA, EMA, and client audits
• Oversee process validation activities for inspection equipment, labeling systems, packaging lines, and serialization/aggregation systems
• Review and approve change controls, risk assessments, and validation protocols/reports impacting inspection, labeling, and packaging operations
• Support QA floor oversight as an SME for escalations during inspection, labeling, and packaging operations
• Stay current with evolving regulatory expectations and industry best practices for parenteral product inspection, labeling, packaging, and serialization

• Bachelor’s degree in a scientific, engineering, or technical discipline (e.g., Biology, Chemistry, Pharmaceutical Sciences, Engineering) required, or 10+ years experience in a Quality and/or Engineering role with similar responsibilities in lieu of a degree
• Minimum of 5 years of experience in pharmaceutical or biopharmaceutical Quality Assurance, with direct experience in developing and maintaining site or corporate level quality systems for finished product inspection, labeling, packaging, and serialization operations
• Minimum of 3 years of experience in a GMP‑regulated parenteral/sterile injectable manufacturing environment
• Demonstrated knowledge of FDA regulations (21 CFR Parts 210, 211), EU GMP Annex 1, ICH guidelines, inspection guidances (USP and , PDA TRs, and applicable serialization regulations (DSCSA, EU FMD))
• Experience with visual inspection methods (manual and automated), AQL sampling plans, and defect classification systems for injectable drug products
• Strong understanding of quality system elements including deviations, CAPAs, change controls, risk assessments, and document management within a QMS
• Experience supporting deviation investigations…