Sanofi Pasteur Inc.

Lead Production Technician

Swiftwater, PA

Sponsorship not specified$27k-$36kDetected 12 days ago

SAPERPCustomer SupportGMPFDA RegulatoryLeadershipWriting

About the role

With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
The production technician will operate in a cGMP manufacturing area performing equipment set up and operations tasks to meet all standards for safety, quality, and efficiency.

Participates in or leads all aspects of the production process utilizing systems such as iShift, LIMS, Trackwise, Labwatch, Documentum, Metasys, DeltaV, and ERP (including ordering, cycle counting, and inventory transactions).
Supports housekeeping, facility cleaning, and daily manufacturing needs to ensure the manufacturing area remains in an inspection-ready state.
Supports off-shift work as needed.
Identifies deviations, aids in investigations, and performs root cause analysis; ensures implementation of effective corrective and preventative actions (CAPAs).
The Lead Manufacturing Technician is a technical contributor to Flublok/Panblok manufacturing operations.
Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.

HS equiv or Associates with 4+ years in manufacturing or Pharmaceutical experience
Bachelor's with 1+ years in manufacturing or Pharmaceutical experience
supports updates and revisions to these documents as required.
Ensures all materials required for production are available prior to need and that the team is planning and working ahead according to the B55 production schedule.
Accurately and timely completes quality documentation including eBRs, logbooks, deviation investigations, and other required records
reviews documentation for completeness and releases commodities as required.
Ensures sampling and corresponding documentation are completed as required.

Prior or related cGMP, Pharmaceutical, or other industrial quality management experience
Proficiency in any of the following areas preferred: Batch record review, environmental monitoring, logbook review, technical writing, SAP, PI historian.
Requires good mechanical skills, computer skills and is detail-oriented.
Must have basic mechanical aptitude, good comprehension skills, retention skills, troubleshooting, and manual dexterity.
Bring the miracles of science to life alongside a supportive, future-focused team.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Sanofi US Services 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

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.
Employees may be eligible to participate in Company employee benefit programs.
Additional benefits information can be found through the LINK.

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.
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth.

ual opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity

This listing is sourced directly from Sanofi Pasteur Inc.'s careers page and normalized into a canonical job model.