Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

Job Title: Manager Filling & Pkg Staff US (2nd Shift)

• Location: Swiftwater, PA

About the Job

This is a 2nd shift position: 2:00pm to 10:00 pm and the candidate must be available to work during weekends and holidays as needed.

 We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.

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

• Manages people process within a process/product team to meet goals and priorities.

• Assures those operations are conducted in compliance with regulatory authorities.

• Responsible for the packaging operations of syringes and vials vaccines to meet established requirements.

• Assures that operations are conducted in compliance with cGMPs, CBER, WHO, EP, and other regulatory bodies.

• Plans and initiates the overall production schedules, coordinating personnel activities with other Manufacturing staff.

• Reviews batch records for correctness and completeness.

• Overall responsibilities include employee selection, training, development, counseling recommendations for cost reductions, profit improvement opportunities, cost control, quality of product, incident investigations, managing departmental capital and operation's budgets.

• Chief duty involves providing managerial coverage for employees as required during third shift working hours.

• Additional responsibilities include determining and presenting technical process improvements and communicating issues to appropriate groups (e.g., IOC, PCUs , staff meetings), and working for unit teams.

• When necessary, coordinates Maintenance, Metrology, and Validation activities with applicable leaders.

• Takes a role in implementing new equipment and procedures. Performs all other duties as required by department management.

• Deviation management, people development, and Quality Assurance of the Packaging Vaccines manufacturing area are required.

About You

Basic Qualifications

• Minimum: High School Diploma/GED with 5+ years of experience in a cGMP or similar regulated environment

• Preferred: Bachelor's degree with 3+ years of experience in a cGMP or similar regulated environment

• Must have previous experience in working with a production department of a pharmaceutical company.

• The candidate must be able to work overtime and flexible hours, including weekends.

Technical Skills:

• cGMP Compliance

• Batch Record Review

• iShift (SAP)

• Deviation Management

• Continuous Improvement (Lean/Six Sigma, SMS or related methodologies)

Soft Skills:

• Leadership

• Cross-functional Collaboration

• Problem-solving

• Communication

• Decision-making

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 and wellness 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 and Affirmative Action employers committed to a culturally diverse 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

#LI-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.

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com