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Senior Production Technician

Sanofi
Swiftwater, PA, United States, United Statesfull_timeVerifiedPosted 3 Jul 2025

About the role

Job title: Senior Production Technician

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. 

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?​

Position Overview:

This is a first-shift position in SEED.

Main Responsibilities:

  • Performs production in accordance with volume fluctuation, business need, and effective procedures. 

  • Ensures all materials required for production are available prior to need. 

  • Ensures the completion of sampling and corresponding documentation as required.

  • Ensures the completion of move tickets and picklists in an accurate and timely manner to ensure accurate inventory. 

  • Participates or leads in all aspects of the production process (SAP, cycle counting, LIMS, Trackwise, Ordering, Labwatch, Qualipso, Metasys, etc.).

  • Works to resolve all production issues. 

  • Understands the next steps and works to guide others through the process to complete them. 

  • Understands the science behind process steps and technology.

  • Ensures all areas within the facility are adequately covered at all times. 

  • May serve as processing room leads and strive to become experts in their assigned areas. 

  • Completes tasks and corresponding documentation as required by cGMP

  • Continues development by completing at least one developmental class annually. 

  • Works to become trained in all assigned training modules.

  • Train and guide Personnel in proper work procedures, use of equipment, cGMP’s, safe work techniques and SAP to assure timely qualifications and consistency in training.

  • Maintains qualified trainer status.

  • Follows all procedures put into effect to ensure your safety as well as the safety of others. 

  • Participates in monthly safety meetings. 

  • Reports all safety issues, concerns, incidents, and near misses to the team leader. 

  • Actively participates in safety walkthroughs coordinated by the department’s safety team. 

  • Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions.

  • Works with the safety team to ensure that the team is completing regular walkthroughs and is taking the necessary steps to address issues. 

  • Works with the safety team to ensure that the resources required to address safety issues are secured in a timely manner and that the effective resolutions are put into place and trained upon. 

  • Works with the safety and leadership team to implement all safety initiatives by actively and effectively communicating the initiatives and by helping others to understand the initiatives.

  • Ensures training is completed on all safety implementations.

  • Follows effective procedures to ensure the production of a safe and efficacious product. 

  • Has a thorough working knowledge of the cGMP’s and works to help others understand. 

  • Identifies areas of deficiency and offers suggestions for improvements. 

  • Identifies deviations and aids in investigations and root cause analysis. 

  • Works to complete quality documentation (Electronic Logbooks and Batch Records) accurately in a timely manner. 

  • Review quality documentation for completeness. 

  • Understands the function of the quality group and works with them to maintain a positive rapport. 

  • Participates in cross-functional teams where necessary to complete projects in an effective and timely manner.

  • All other duties as assigned.

About You

Basic Qualifications:

  • HS diploma or equivalent and 3+ years in cGMP or Pharmaceutical experience

  • Associates with 2 + yrs in cGMP or Pharmaceutical experience

  • Bachelors with 1 + yrs in cGMP or Pharmaceutical experience

Preferred Qualifications:

  • Prior or related cGMP or Pharmaceutical experience recommended

  • Proficiency in at least two areas of operations or pr

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Company

Sanofi

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