Validation Specialist

Your Opportunity Our Bio/Pharmaceuticals group brings together innovative and functional design solutions for companies involved in the discovery, research and development, and commercial scale manufacturing of pharmaceuticals, biotechnology, and medical device products. This is where great people and great ideas truly make a difference. Our team has a keen understanding of the critical issues facing the industry and its complex regulatory demands, and brings together a range of expertise, specializing in the consulting, planning, designing, engineering, commissioning, and validation of projects. We deliver a full range of archtiectural, engineering, and compliance services-and allow you to set the pace of your career.

Stantec has an exciting opportunity in our Hauppauge, NY office for a Validation Specialist. The client location for this position is San Jose, CA therefore the successful candidate could also be based in any of our offices in the surrounding area such as Los Gatos, San Francisco, or Walnut Creek, CA.

Your Duties The candidate will be responsible for developing and executing equipment and utility/HVAC system commissioning and validation (IQ/OQ/PQ) protocols with specific experience in Pharmaceutical manufacturing facility/HVAC/process equipment in accordance with Good Engineering Practices, client SOP's, industry best practices and other industry related guidance documents. Sterile manufacturing experience for validation of equipment and/or utility/HVAC systems is preferred.

Your Capabilities and Credentials

  • BA or BS in Engineering or Scientific related field preferred
  • At least 3 years of experience with Commissioning and Qualification/Validation within the Bio/Pharm industry a must
  • Candidate must be able to travel extensively within US, Puerto Rico and Canada as required for execution of existing and new Commissioning and Validation work
  • Candidate must have experience in working with Microsoft Office applications.



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