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Senior Manager, Drug Product Optical Inspection System User

Job in Wichita, Sedgwick County, Kansas, 67232, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-03
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Quality Engineering, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below

Job Function

Supply Chain Manufacturing

Job Sub Function

Manufacturing Pharmaceutical Process Operations

Job Category

Professional

All Job Posting Locations

Wilson, North Carolina, United States of America

Job Description About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Job Summary

As a member of this new team, the role will partner closely with parenteral Drug Product sites across the J&J network and will own and drive the end‑to‑end recruitment ramp‑up strategy, delivering results in alignment with project timelines and budget commitments. This role will transition from a single contributor role into a Senior Production Manager role with responsibility for the Optical Inspection operations team.

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), with specific focus 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 appropriately 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…
Position Requirements
10+ Years work experience
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