Production Tech - Syringes

Biopharma Careers; Swiftwater (MS); On-site; USD 42,000 - 54,000; Full time

Job summary

Sanofi Pasteur is seeking a Production Tech - Syringes to support manufacturing operations on a rotating 3rd shift in Swiftwater, PA. You will perform production activities, ensure material readiness, and maintain cGMP documentation to support high-quality vaccine product output.

Ideal candidates have 2+ years in cGMP/pharmaceutical environments, with HS equiv and relevant degrees. SAP data entry and cross-training across areas are part of the role.

Qualifications

• HS equivalency and 2+ years in cGMP or pharmaceutical experience.
• ,
• ],

Responsibilities

• Perform production activities in accordance with volume fluctuations and procedures.
• Ensure materials required for production are available in advance.
• Identify production issues and report them to leadership.
• Complete cGMP documentation accurately and timely.
• Train and orient new team members as assigned.
• Participate in safety meetings and report issues.
• Input data into SAP and manage work orders.

Skills

cGMP experience

Pharmaceutical experience

Ase

Education

HS equiv

Associate degree

Bachelor's degree

Tools

SAP

Job description

Job title: Production Tech - Syringes

Location: Swiftwater, PA

THIS IS A ROTATING 3RD SHIFT POSITION.

About the job

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.

Sanofi Pasteur, the vaccines division of Sanofi, provides more than 1 billion doses of vaccine each year, making it possible to immunize more than 500 million people across the globe. A world leader in the vaccine industry, Sanofi Pasteur offers a broad range of vaccines protecting against 20 infectious diseases. The company’s heritage, to create vaccines that protect life, dates back more than a century. Sanofi Pasteur is the largest company entirely dedicated to vaccines. Every day, the company invests more than EUR 1 million in research and development. For more information, please visit: www.sanofipasteur.com or www.sanofipasteur.us

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 people’s lives.

Main 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.
• Report all safety issues, concerns, incidents and near misses to the team leadership.
• 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.). FDA audit understanding and awareness.
• 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.
• Lead Operator, Completes picklists and move tickets for all tasks completed on any given day.
• This may require inputting data into SAP, along with entering work orders and reagent orders.
• 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 were warranted. Write and edit 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.

About You

Requirements

• HS equiv and 2+ years in cGMP or Pharmaceutical experience
• Associates with 1 + yrs in cGMP or Pharmaceutical experience
• Bachelors with 0 + yrs in cGMP or Pharmaceutical experience
• Must successfully pass Ase