Senior Manager, Drug Product Optical Inspection System User

Senior Production Manager – Optical Inspection Operations, Wilson, North Carolina, United States Key Responsibilities Serve as the recognized Subject Matter Expert (SME) for Optical Inspection across the Drug Product facility, providing end-to-end technical ownership for manual and automated visual inspection processes for parenteral products. Lead and actively participate in all safety-related reviews (HAZOP, machine safety, ergonomic and human-factors assessments), focusing on inspection systems, operator interfaces, and defect-handling risks. Own the review and approval of User Requirement Specifications (URS) for optical inspection systems, ensuring alignment with cGMP, global regulatory expectations, inspector qualification requirements, and product quality standards. Review and approve engineering deliverables from concept through detailed design (e.g., PFDs, P&IDs, functional design specifications, equipment and automation specifications), acting as the final technical authority for inspection-related decisions. Define, govern, and continuously improve defect libraries, inspection standards, acceptance criteria, and inspection strategies, including challenge and approval of critical defect classifications and assumptions. Author, review, and approve process support and operational documentation, including Master Batch Records, SOPs, Work Instructions, inspection test kits, defect standards, and inspector qualification materials. Provide active on-site support during commissioning, qualification, and validation activities, including engineering studies, water and engineering batches, aseptic process simulations (APS), and validation batches, ensuring inspection readiness and compliance. Lead the preparation, execution, review, and approval of validation documentation related to optical inspection systems, including IQ/OQ/PQ, inspector qualification, and ongoing performance monitoring. Act as the quality-facing SME during regulatory inspections, audits, and internal reviews, confidently representing inspection strategies, data integrity, and compliance posture, and driving resolution of complex inspection-related observations. Ensure digitalization, automation, and robotics solutions for inspection are evaluated, selected, implemented, and standardized, staying current with emerging technologies and industry best practices. Identify required spare parts, critical components, and consumables for optical inspection and associated support systems, coordinating procurement and lifecycle management with engineering, operations, and supply chain partners. Ensure delivery of all inspection-related activities within approved budget and project schedules, proactively identifying and mitigating technical, regulatory, and operational risks. Monitor and verify that all user requirements, regulatory expectations, and quality commitments are met, including timely completion of information requests, documentation approvals, and readiness milestones. Develop and execute training and qualification plans for inspectors, engineers, and operations personnel, ensuring sustained inspection capability and compliance. Qualifications Education: Bachelor’s or higher degree in Life Sciences, Pharmacy, or Engineering (required). Master’s or higher degree preferred. Experience: Minimum of 8 years in the pharmaceutical industry, including people leadership. Minimum of 3+ years serving as the recognized SME in Optical Inspection for parenteral filled products, with deep expertise in manual and automated visual inspection systems, test kits, defect libraries, and inspector qualification programs. Expert-level knowledge of cGMP regulations and proven record of leading inspections, audits, and regulatory interactions. Advanced expertise in digitalization, automation, and robotics technologies, with demonstrated ability to evaluate, select, implement, and standardize advanced technologies. Demonstrated thought leadership and innovation, with a track record of originating, championing, and implementing novel technical solutions. Exceptional interpersonal and influencing skills, with ability to act as the go‑to technical authority across cross‑functional, site, and global teams. Strong analytical, problem‑solving, stress tolerance, decision‑making, and entrepreneurial mindset. Preferred: Lean/Six Sigma certifications. Preferred Skills Agile Manufacturing, Business Intelligence (BI), Change Management, Chemistry, Manufacturing, and Control (CMC), Competitive Landscape Analysis, Consulting, Cost‑Benefit Analysis (CBA), Developing Others, Gap Analysis, Good Manufacturing Practices (GMP), Industry Analysis, Manufacturing Standards, Operational Excellence, Organizational Knowledge, Organizing, Plant Operations, Process Optimization, Program Management, Technical Credibility. Location and Travel Position will be located in Wilson, North Carolina, requiring full‑time on‑site support. During the design phase, the role will operate primarily at an engineering firm with frequent travel (>75%) until the project shifts to the Wilson plant site. Equal Opportunity Employment Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource. #J-18808-Ljbffr