Sanofi

B55 Operations Manager - 2nd Shift

Sanofi$90K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • High school diploma with 5+ years in Biotechnology or Pharmaceutical Manufacturing or cGMP environments.
  • Experience within a quality or production department of a Biotechnology/Pharmaceutical company.
  • Strong cGMP knowledge and application.
  • Effective communication and interpersonal skills.
  • Proven ability to work on cross-functional project teams.
  • Track record of meeting or exceeding timelines and deliverables.
  • Familiarity with continuous improvement techniques and strong analytical problem-solving skills.

Responsibilities

  • Manage multiple priorities independently and collaboratively to meet deadlines.
  • Communicate updates and issues at all organizational levels.
  • Promptly resolve quality assurance observations to uphold product standards.
  • Conduct monthly health, safety, and environment audits and investigations.
  • Perform GEMBA walks to enforce compliance and quality assurance.
  • Support the closure of deviations to ensure continuous improvement and compliance.
  • Oversee batch record sections and final review to achieve production targets.

Benefits

  • Join a supportive and forward-thinking team working to bring scientific innovations to life.
  • Countless opportunities for career advancement within the company, including international options.
  • Comprehensive benefits package that values employee contributions.
  • Access to a wide range of health and wellness benefits, including premium healthcare and 14 weeks of parental leave.
  • Engage with cutting-edge technology in shaping the future of medicine and vaccine delivery.
  • Utilize digital tools and AI to drive high performance in operations.
Full Job Description

Job Title: B55 Operations Manager - 2nd Shift

  • Location: Swiftwater, PA

About the Job

The Manager, B55 Recombinant Manufacturing Facility (RMF) will provide the leadership, direction, and the overall oversight of theB55 RMF department on 1st shift at the Swiftwater, PA site. This position is responsible for operational and project results ofB55 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.

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 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, 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 Manufacturingor 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 Qualifications

  • Experience with the management of direct reports.

  • Experience in Viral manufacturing and/or Bacterial Manufacturing

  • Leadership, people development, driving the right culture and mindset (10+ people report to this position, helping to drive Tier 1 Site Projects)

  • Operational Excellence 6 Adaptation and driving the use of SMS tools, continuous improvement, cost savings, inventory control (SAP / S4), Digital and AI 6 Openness

  • Quality and Compliance 6 regulatory audit experience, driving compliance performance (deviation elimination, implementation of CAPAs to improve or error proof). Root cause analysis and Change Management. Experience in driving an initiative or project to completion as an owner

  • Able to work with multiple stakeholder groups, adaptable (ability to respond to changes in initiative / timeline / priority)

Special Working Conditions

  • Ability to lift to 50 lbs.

  • Ability to stand on average 8 hours per shift.

  • Ability to gown and gain entry to manufacturing areas.

  • Ability to work a twelve-hour rotating shift and every other weekend, including holidays as scheduled.

  • May require personnel to flex into another platform within MTech and/or another MS department, as well as the possibility to work weekends, holidays or off shift hours based on business need.

  • May also include working in an aseptic processing area.

Why Choose Us?

  • Bring the miracles of science to life alongside a supportive, future-focused team.

  • Discover endless opportunities to gain experience and drive your career, whether it9s 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 diligent 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 weeks9 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 6 at speed and scale.

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. Additional benefits information can be found through the .

About Sanofi

Sanofi is a global pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs and vaccines. The company operates in over 170 countries and has a diverse portfolio of products that includes treatments for diabetes, cancer, cardiovascular disease, and rare diseases. Sanofi is committed to improving global health and has a strong focus on innovation and sustainability. The company has received numerous awards for its research and development efforts and is recognized as a leader in the pharmaceutical industry.
Learn more about Sanofi
Market Cap
$121.6 billion
Industry
Net Income
$12.3 billion
Founded
1990
5 Year Trend
+2.5%
Revenue
$37.3 billion
NASDAQ

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