Visual Inspection Manager 2nd Shift

Job Title: Visual Inspection Manager 2nd Shift

Location: Swiftwater, PA

This is a 2nd Shift leadership role.

About The Job The Manager, Visual Inspection Operations provides hands-on leadership and strategic oversight of visual inspection operations within a regulated vaccine manufacturing environment. This role is accountable for safety, quality, delivery, cost, and people performance while fostering a culture of ownership, compliance, and continuous improvement. The ideal candidate is an experienced visual inspection leader who sets clear expectations, holds teams accountable to defined standards, and drives measurable performance improvements. This individual brings strong technical knowledge of manual and automated inspection processes and leverages industry best practices to strengthen systems, elevate inspector capability, and enhance operational efficiency.

This leader serves as a change agentdeveloping talent, improving processes, reinforcing right-first-time execution, and elevating inspection excellence across the shift.

Join a global network that powers how Sanofi delivers seamlessly, purposefully, and at scale. In Manufacturing & Supply, youll help reimagine how life-changing treatments reach people everywhere, faster.

About Sanofi Were an R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives.

Main Responsibilities

Safety Follows all procedures put into effect to ensure your safety as well as the safety of others. Participates in monthly safety meetings.

Reports all safety issues, concerns, incidents and near misses to the team leadership.

Actively participates in safety walkthroughs coordinated by the departments safety team.

Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.

Follows effective procedures to ensure the production of a safe and efficacious product.

Utilizes +QDCI boards for Safety issues

Leads Safety Meetings.

Quality FDA audit understanding and awareness. Ensures areas are always following proper procedures

Identifies possible deviation occurrences and prevents or aids in investigations and root cause analysis.

Ensure compliance with cGMP, FDA, EU Annex 1, and regulatory requirements.

Review batch records and inspection documentation for accuracy and completeness.

Lead preliminary deviation investigations and support root cause analysis.

Support internal and external audits and regulatory inspections.

Maintain inspection standards and ensure audit readiness.

Delivery Performs production in accordance with volume fluctuation, business need, and effective procedures.

Must be flexible to ensure staffing for changing business volume and needs

Lead visual inspection operations during 2nd shift.

Establish clear expectations and drive accountability across the team.

Cost Executes procedure as documented to avoid deviations.

Oversee production planning and scheduling to meet throughput and quality targets.

Drive efficiency improvements, waste reduction, and process optimization initiatives.

Implement best practices from industry benchmarking and prior experience.

Lead or support automation initiatives for visual inspection systems.

Collaborate cross-functionally with Manufacturing, Quality, Engineering, and Supply Chain.

Involvement Has a thorough working knowledge of cGMPs and works to help others understand.

Lead in Shift Change.

Maintains acceptable training as described in key requirements.

Coach, develop, and mentor inspectors and frontline leaders.

Manage recruitment, onboarding, training, and performance management.

Foster a culture of engagement, ownership, and continuous improvement.

All other duties as assigned.

About You Basic Qualifications

Bachelor's degree in any field, OR 5 years of equivalent experience in pharmaceutical operations.

Minimum 5 years of relevant experience in pharmaceutical or biologics manufacturing

Minimum 2 years of team leadership experience (managing direct reports)

Strong knowledge of cGMP requirements and quality systems.

Demonstrated ability to drive accountability and performance improvement.

Experience leading root cause investigations and implementing corrective actions

Preferred Qualifications Direct visual inspection experience in a GMP-regulated environment

Experience with manual and automated inspection processes

Experience in high-volume manufacturing operations

Why choose us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether its through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention andwellness programs and at least 14 weeks gender-neutral parental leave.

Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.

Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale

Transform lives worldwide by delivering life-changing treatments anywhere, anytime.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.