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B55 Operations Manager - 2nd Shift

Job in Pittsburgh, Allegheny County, Pennsylvania, 15289, USA
Listing for: Eacademy Sanofi
Full Time position
Listed on 2026-06-24
Job specializations:
  • Manufacturing / Production
    Production Manager
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Job Title
: B55 Operations Manager - 2nd Shift

Location

Location: Swiftwater, PA

About the Job

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.

The Manager, B55 Recombinant Manufacturing Facility (RMF) will provide the leadership, direction, and the overall oversight of the B55 RMF department on 1st shift at the Swiftwater, PA site. This position is responsible for operational and project results of B55 operations, including safety, quality, supply, and costs as well as employee engagement and management.

Sanofi is seeking a highly skilled and experienced Manager to oversee our manufacturing processes. The ideal candidate will have outstanding organizational and leadership skills, a firm grasp of manufacturing processes and standards, and the ability to ensure that our manufacturing processes deliver products of maximum quality.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing Progress to make a real impact on millions of patients around the world.

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and  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 people’s lives.

Main Responsibilities
  • Manage Multiple priorities independently or as part of a team to meet key deadlines.
  • Communicate issues and progress across all levels of the organization.
  • Resolve QA shop floor observations promptly to maintain product quality.
  • Perform monthly HSE audits, complete HSE investigations, and provide support for HSE Corrective and Preventive Actions (CAPAs).
  • Perform GEMBA Walks to ensure strict adherence to quality and compliance in our facilities.
  • Support Deviation closures to ensure compliance and continuous improvement.
  • Support CAPAs, Change Controls, internal audits and any other regulatory commitments.
  • Execute Batch Record Sections and Final Review in a timely manner in order to hit production targets.
  • Manage +QDCI L1 boards to meet company KPIs and drive change. Establish performance expectations and evaluate direct reports.
  • Manage employee development goals to foster growth and skill. Support a culture of teamwork.
  • Drive efficiently in communication between employees through shift change huddles.
  • Manage personnel attendance using Labor Utilization Role-Based Schedule Tool, ADP, Workday.
  • Actively involved in onboarding new hires to ensure smooth integration.
  • Monitor Metasys/Lab watch applications to ensure GMP status of the production floor.
  • Serve as an escalation point and make decisions to resolve issues promptly.
  • Responsible for project work on the shop floor, provide assistance and recommendations regarding processes or equipment.
  • All other duties as assigned.
About You

Required Qualifications
  • High school diploma with a minimum of 5 years of experience that includes:
    Biotechnology, Pharmaceutical Manufacturing or cGMP experience.
  • Working within a quality or production department of a Biotechnology/ Pharmaceutical company.
  • cGMP experience.
  • Excellent communication and interpersonal skills.
  • The ability to work on cross functional project teams.
  • Demonstrated ability to meet/exceed timelines/deliverables.
  • Continuous improvement techniques and problem solving/analytical skills.
  • Ability to negotiate/Influence.
  • Organized and detail oriented.
Preferred…
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