Validation Engineer

Role: Manufacturing Validation Engineer – Commissioning (3DP Installations)
Location: Raynham, Massachusetts (Onsite)
Duration: Full Time.

Role Overview
We are seeking experienced Validation Engineers to support commissioning activities for 3D Printing (3DP) installations within a MedTech/Pharma manufacturing environment. This is a fully onsite role requiring strong hands-on experience in equipment and process validation.

Key Responsibilities
Support commissioning, qualification, and validation (CQV) activities for 3DP equipment.
Execute and review validation documentation including IQ, OQ, and PQ protocols.
Collaborate with cross-functional teams including Engineering, Quality, and Operations.
Ensure compliance with GMP, FDA, and internal quality standards.
Perform equipment and process validation for manufacturing systems.
Support troubleshooting and resolution of validation and commissioning issues.
Contribute to continuous improvement initiatives across validation processes.

Required Experience & Skills
5+ years of experience in validation within MedTech or Pharmaceutical environments.
Strong experience with equipment validation and commissioning activities.
Proven experience in process validation (IQ/OQ/PQ execution).
Familiarity with GMP, FDA, and regulatory requirements.
Experience working with manufacturing equipment (3DP experience is an advantage).
Strong documentation and communication skills.
Ability to work onsite in a fast-paced project environment.

Preferred Qualifications
Experience with advanced manufacturing technologies (e.g. 3D Printing).
Exposure to digital validation tools or automation environments.
Degree in Engineering or a related technical discipline.

What We Offer:
Opportunity to work on cutting-edge 3DP technology.
Exposure to leading MedTech/Pharma projects.
Collaborative and dynamic project environment.
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