Visual Inspection Manager 3rd shift

BioSpace

Swiftwater (Monroe County)

On-site

USD 110,000 - 160,000

Full time

1 hour ago
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Benefits offered by this job

Health benefits
Parental leave (14 weeks)
Opportunity for career growth

Job summary

Sanofi Inc. in Swiftwater, PA, is seeking a Visual Inspection Manager for the 3rd shift to lead and optimize inspection operations in a regulated vaccine manufacturing environment.

The role emphasizes safety, quality, and continuous improvement while driving accountable performance and right-first-time execution. The ideal candidate brings hands-on leadership, strong knowledge of manual and automated inspection, and a track record of process improvements across shift-based teams.

Qualifications

  • Minimum 3 years of relevant pharma/biologics manufacturing experience.
  • Strong knowledge of cGMP requirements and quality systems.
  • Experience leading root cause investigations and implementing corrective actions.

Responsibilities

  • Lead visual inspection operations on 3rd shift.
  • Ensure safety, quality, delivery, cost, and people performance.
  • Coach and mentor inspectors and frontline leaders; recruit and train staff.

Skills

Team leadership
Quality systems
cGMP knowledge
Root cause investigations

Education

Bachelor's degree in Life Sciences/Engineering

Job description

Job Title: Visual Inspection Manager 3rd shift

Location: Swiftwater, PA

About The Job

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

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.

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 following proper procedures at all times

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
  • Minimum of High School Diploma.
  • Minimum 3 years of relevant experience in pharmaceutical or biologics manufacturing.
  • Demonstrated team leadership experiencewhich may include formal supervisory roles or informal leadership such as directing the work of others, coordinating shift or cross-functional activities, training and mentoring team members, or acting as a lead or designee for a manager.
Technical Skills
  • 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
  • Bachelors degree in Life Sciences, Engineering, or related field (or equivalent experience).
  • Experience leading visual inspection operations across multiple organizations or sites.
  • Proven success implementing process improvements that enhance efficiency, quality, or compliance.
  • Experience with automated or semi-automated inspection systems.
  • Knowledge of iSHIFT, eBR systems, or inspection management software.
  • Demonstrated success developing high-performing inspection teams.
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.

#GD-SP
#VHD

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.

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