Visual Inspection Manager - 3rd Shift

Sanofi Group; Pennsylvania; Hybrid; USD 90,000 - 130,000; Full time

Benefits offered by this job

14 weeks’ gender-neutral parental leav

Healthcare benefits

Job summary

Sanofi Group in Swiftwater, PA is seeking a Visual Inspection Manager for 3rd shift. You will provide hands-on leadership and strategic oversight of visual inspection operations in a regulated vaccine manufacturing environment, ensuring safety, quality, delivery, cost, and people performance.

You will drive continuous improvement, coach inspectors, and lead cross-functional collaboration with Manufacturing, Quality, Engineering, and Supply Chain.

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.
• Preferred: Direct visual inspection experience in a GMP-regulated environment.

Responsibilities

• Safety: follow procedures, participate in monthly safety meetings, report safety issues, participate in safety walkthroughs, input for corrective actions.
• Quality: maintain cGMP compliance, review batch records, lead deviation investigations, support audits and regulatory inspections, ensure audit readiness.
• Delivery: lead visual inspection operations on 3rd shift, adjust staffing for volume, drive throughput and quality targets.
• Cost: oversee production planning to meet targets, drive efficiency and waste reduction, implement best practices, support automation initiatives.
• Involvement: maintain training, coach and mentor inspectors, recruit and onboard, foster engagement and continuous improvement.

Skills

Visual inspection leadership

cGMP knowledge

Safety leadership

Cross-functional collaboration

Education

Bachelor's degree or 5 years pharma ops experience

Job description

Job Title Visual Inspection Manager Location: Swiftwater, PA This is a 3rd 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 agent—developing 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, you’ll help reimagine how life-changing treatments reach people everywhere, faster. About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s 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 department’s 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 3rd 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 cGMP’s 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. 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 it’s 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; colour; 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 #LI-SP #VHD Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. Sanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here US and Puerto Rico Residents Only 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. North America Applicants Only The salary range for this position is: $90.000,00 - $130.000,00 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. Wir sind ein forschendes Biopharma-Unternehmen, das KI anwendet und sich dafür einsetzt, das Leben der Menschen zu verbessern und verantwortungsvoll zu wachsen. Unser Team wird von einem Ziel geleitet: Wir erforschen die Wunder der Wissenschaft, um das Leben der Menschen zu verbessern. Wir möchten eine gesündere, widerstandsfähigere Welt schaffen und das Unmögliche möglich machen, indem wir Medikamente und Impfstoffe für Millionen von Menschen weltweit entdecken, entwickeln und bereitstellen. Erfahren Sie mehr über uns auf www.sanofi.com oder schauen Sie sich unseren Film an: We are Sanofi Starte eine Karriere, die einen Unterschied macht. Neuerfindung liegt in unserer DNA. Sie hat unsere Entwicklung von einem kleinen französischen Unternehmen zu einem der weltweit führenden Biopharma-Unternehmen vorangetrieben. Ob es darum geht, KI zu nutzen, um die Zeiten der Arzneimittelforschung zu verkürzen, oder Vertrauen im Gesundheitswesen aufzubauen – du kannst unseren Teams dabei helfen, das Leben für Patient*innen, Partner*innen und Gemeinschaften zu verbessern. Hier entwickelst du deine Karriere weiter. Wir öffnen dir die Tür, um neue Möglichkeiten zu entdecken, deine Grenzen zu erweitern und dich mit Menschen zu vernetzen, die von einem gemeinsamen Ziel angetrieben werden: Wir erforschen die Wunder der Wissenschaft, um das Leben der Menschen zu verbessern.