Vaccine Manufacturing Manager Production Influenza Bulk Drug Substance Upstream 2nd Shift
Sanofi is hiring a Vaccine Manufacturing Manager Production Influenza Bulk Drug Substance Upstream 2nd Shift. It pays $90k-$130k a year and Level rates it ; you can apply on Sanofi.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- The posting mentions Adp, Workday and Metasys among its tools and skills.
- Level classes it as a mid-level role.
- Sanofi has 1,000+ other open roles on Level.
AI in this role
Manage vaccine manufacturing processes, production schedules, quality compliance, and team development for influenza bulk drug substance upstream.
Job Title: Vaccine Manufacturing Manager Production Influenza Bulk Drug Substance Upstream 2nd Shift
- Location: Swiftwater, PA
About the Job
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.
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
- 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.
About You
Basic Qualifications
- 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.
Skills:
- 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.
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 M&S 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 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.
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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 - $130.000,00All 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.
How we rate this
Vaccine Manufacturing Manager Production Influenza Bulk Drug Substance Upstream 2nd Shift at Sanofi rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where manufacturing was part of your work. What did you do?
- Tell me about a project where leadership was part of your work. What did you do?
- Tell me about a project where quality assurance was part of your work. What did you do?
- Tell me about a project where hsi audits was part of your work. What did you do?
- Tell me about a project where production management was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Manufacturing, Leadership, Quality Assurance, Hsi Audits, and Production Management. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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