Manager, Visual Inspection

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

As the Manager, Visual Inspection, you'll report directly to the Director of Operations and oversee a dedicated team of visual inspection and packaging technicians across three manufacturing sites. You'll be responsible for the final steps in delivering life-changing medicines-ensuring products are properly inspected, documented, packaged, and shipped in compliance with cGMP and internal SOPs.

What You'll Do:

• Lead and develop a team of up to 15 technicians, ensuring compliance, efficiency, and excellence in inspection and packaging operations.

• Own and manage the Visual Inspection Operator Qualification Program, ensuring adherence to the latest regulatory standards.

• Serve as the Subject Matter Expert (SME) during audits by clients and regulatory agencies.

• Monitor daily inspection, labeling, and bulk packing activities to ensure timely and accurate product release.

• Investigate deviations, drive root cause analysis, and implement corrective actions.

• Track and report on key metrics including defect rates, inspection throughput, and delivery performance.

• Collaborate cross-functionally with Quality, Validation, and Facilities to meet production and compliance goals.

• Promote a culture of continuous improvement through training, process enhancement, and meticulous recordkeeping.

Who You'll Work With:

You'll collaborate closely with team members in Operations, Quality Assurance, Validation, and Facilities, as well as key external vendors.

What You Bring:

• Bachelor's degree in a related scientific or technical field

• 4+ years of relevant experience in sterile parenteral manufacturing and 2+ years in a supervisory role

• Deep expertise in Visual Inspection of both liquid and lyophilized parenteral products

• Hands-on experience with aseptic processing and GMP-regulated environments (FDA/EU)

• Strong communication, documentation, and leadership skills

• Proficiency with Microsoft Office (Word, Excel, PowerPoint)

• Ability to coach, mentor, and inspire a high-performing team

Why Join Us?

You'll be part of a collaborative, mission-driven organization committed to delivering critical therapies to patients around the globe. We offer a supportive culture, competitive compensation, and growth opportunities across departments.

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Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.