The Opportunity

We're looking for a Validation Specialist III, working in the Pharmaceuticals & Medical Products industry in Swiftwater, Pennsylvania, United States.

  • Establish dirty hold times and clean hold times.
  • Determine sampling procedures, plans and sample sizes.
  • Apply bracketing and worse case rating.
  • Review and analyze data.
  • Defend rationale in validation documents.

We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.

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
  • Proficiency in utilizing documentation system to author protocols and reports
  • Experience participating in teams and collaborative work environments
  • Good communication skills (verbal and written), math skills and general computer skills
  • Working knowledge of templates, workflows and approval process
  • Strong root cause analysis with cGMP experience
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 here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.


Optional. 20 MB file size limit. Supported file types.

Upload your Resume
I have read and accepted the Terms & Privacy Policy
I agree to be part of PSG's Talent Community and be profiled to other jobs that match my skills