Lead Production Technician, Swiftwater, PA-

Job Title: Lead Production Technician, Swiftwater, PA-

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. Your job, as Lead Production Technician, within our Formulation Team will be to perform formulation preparation and process activities in accordance with volume fluctuation, business need, and effective procedures in assigned areas. This includes aseptic closed system processing and working in a cGMP environment.

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?

Main Responsibilities

• SAP transactions (ordering supplies, inventory management, work orders, complete pick lists and process orders, cycle counts, schedule and confirm phases)
  
• Trained as a manager/designee an performs all associated functions
  
• Formulation skid prep (CIP/SIP) and cross-trained to perform skid operation on all Formulation critical processes; Assumes a lead role in batch processing as required
  
• General maintenance and housekeeping (chart changes, pressure checks, restocking); Monitoring (daily release, environmental monitoring, WFI/CS sampling, cleaning monitoring)
  
• Deviation investigation writing, CAPA, and internal audit writing and action item ownership; support closure of CCR action items
  
• Support regulatory inspections and projects as needed as SME
  
• Completes batch record transcription and prepares batch record for manager review; manage retro-release of buffers and control of inventory and use; manager/designee
  

Context of the job/major challenges

• Ensures all materials are available and preparation activity required for upcoming production is complete prior to need.
  
• Identifies production issues and relays them to the leadership team. Completes safety and quality audits as scheduled.
  
• Ensures training is complete prior to completing tasks.
  
• Completes GMP documentation right first time. Assists in deviation investigations and implementation of CAPA plans.
  

About You

Basic Qualifications:

• HS equiv and 5+ in cGMP or Pharmaceutical experience
  
• Associates with 3+ in cGMP or Pharmaceutical experience
  
• Bachelor's with 2+ in cGMP or Pharmaceutical experience
  

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.
  

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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