Production Technician Senior

Sanofi • Swiftwater, PA

223d • $19 - $29

About The Position

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. This is a third shift position. 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. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Requirements

• HS/GED with at least 1 year prior manufacturing work experience or Associates degree with prior manufacturing work experience.
• Prior or related cGMP or Pharmaceutical experience recommended.
• Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, manual dexterity, and ability to troubleshoot.

Responsibilities

• Performs production activities in accordance with volume fluctuation, business need, and effective procedures.
• Works to support production units by consistently providing required materials in a timely manner.
• Ensures all materials required for production are available prior to need.
• Identifies production issues and relays them to the leadership team.
• Ensures all required paperwork is complete, accurate and done in a timely manner to ensure accurate inventory.
• Completes tasks and corresponding documentation as required by cGMP.
• Works to prepare assigned areas for the oncoming shifts.
• Completes at least one developmental class annually focused on one of the four core competencies.
• Works to become trained in all assigned training modules.
• Trains and orients new team members (at any level) as assigned.
• 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 leadership.
• 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.
• Follows effective procedures to ensure the production of a safe and efficacious product.
• Works to understand cGMP's.
• Identifies areas of deficiency to the leadership team and offers potential suggestions for improvements.
• Participates in both deviation investigations when appropriate and implementation plans to ensure a quality product.
• May participate in completion of quality documentation (BPR's, logbooks, etc.).
• Participates in team meetings.
• Actively communicates improvement ideas, issues, concerns, etc to team.
• Participates in cross functional teams where necessary to complete projects in an effective and timely manner.
• Completes picklists and move tickets for all tasks completed on any given day.
• Ensures proper process area operation by pre and post run set up and maintenance of lab and equipment.
• Recommends changes to BPRs, SOPS and SWIs where warranted.
• Writes and edits documents under supervision.
• Seeks out cross training in other areas whenever possible.
• Responsible for assisting in writing and assisting incident investigations, CAPA's, change controls, along with assisting the higher tech levels and Principal Investigators with projects.
• All other duties as assigned.

Benefits

• High-quality healthcare
• Prevention and wellness programs
• At least 14 weeks' gender-neutral parental leave

What This Job Offers

• Industry: Chemical Manufacturing
• Education Level: High school or GED