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Validation Specialist – Biotech Downstream Process Equipment
Mentor Technical Group
Full-time
United States, United States
other-general
Posted:
March 03, 2026
Location:
United States, United States, United States
Job Description
Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
Key Responsibilities:
+ Develop, review, and execute validation protocols (IQ, OQ, PQ) for downstream process equipment.
+ Perform risk assessments, gap analyses, and validation reports for new and existing equipment.
+ Collaborate with engineering, QA, and operations teams to ensure equipment meets regulatory requirements.
+ Support commissioning and qualification activities for bioprocess systems, including filtratio...
Key Responsibilities:
+ Develop, review, and execute validation protocols (IQ, OQ, PQ) for downstream process equipment.
+ Perform risk assessments, gap analyses, and validation reports for new and existing equipment.
+ Collaborate with engineering, QA, and operations teams to ensure equipment meets regulatory requirements.
+ Support commissioning and qualification activities for bioprocess systems, including filtratio...
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Submit your application for the Validation Specialist – Biotech Downstream Process Equipment position at Mentor Technical Group.
Apply Now Save for LaterJob Overview
Job Type:
Full-time
Location:
United States, United States
Posted:
March 03, 2026
Deadline:
March 08, 2026