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Validation Specialist III

Location: Swiftwater, PA, United States
Job Type: Full Time
Job Category: Pharmaceutical and Biotech
Job Industry: Pharmaceuticals and Medical Products
Salary: The pay we're offering is $52 - $57 per hour
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The Opportunity


We're looking for a Validation Specialist III, working in Pharmaceuticals and Medical Products industry in 1 Discovery Drive, Swiftwater, Pennsylvania, 18370, United States.

  • Authors and reviews development and validation notebook studies/protocols/reports.
  • Executes studies in pilot plant / manufacturing environment and follows all procedures put into effect to ensure your safety as well as the safety of others.
  • Follows good documentation practices to record all activities performed and data generated in production of developmental experiments.
  • Participates in safety meetings, reports all safety issues, concerns, incidents and near misses to the team leadership.
  • Identifies production issues and relays them to the laboratory management and ensures all required paperwork is complete, accurate and done in a timely manner to ensure a quality product.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

  • Bachelor’s degree in scientific discipline plus 3 to 6 years of experience in vaccine, biologic, or pharmaceutical manufacturing and/or development.
  • MS Office EDoc or Geode, with a working knowledge of templates, workflows and approval process.
  • LabWare/ LIMS experience is preferred.
  • Full understanding of GMP Documentation and current GMP standards Good lab / aseptic technique.
  • Interact well and professionally with a diverse group of individuals.
  • Self-motivated and willing to be proactive in resolving issues.
  • Excellent verbal and written communication skills.
  • Ability to work in a team environment.
  • Ability to write and complete deviations in a timely and thorough manner.
  • Ability to multitask and prioritize tasks.
  • Flexibility of hours during execution to include nights and weekends.

What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply Now

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