Vaccine Manufacturing Manager Production Influenza Bulk Drug Substance Upstream 2nd Shift

Sanofi•Pocono Township, PA
•$90,000 - $130,000•Onsite

About The Position

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. 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.

Requirements

  • Bachelor’s degree with a minimum of 5 years of experience in Quality, Production, manufacturing operations or other related fields.
  • Associates degree with a minimum of 7 years of experience in Quality, Production, manufacturing operations or other related fields.
  • High School degree with a minimum of 10 years of experience in Quality, Production, manufacturing operations or other related fields.
  • Experience with the managing, supervising or leading teams.
  • Experience in Viral manufacturing and/or Bacterial Manufacturing
  • 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.

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 adherent 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, providing assistance and recommendations regarding processes or equipment.
  • All other duties as assigned.

Benefits

  • high-quality healthcare
  • prevention and wellness programs
  • 14 weeks’ gender-neutral parental leave
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