Position Details
About this role
Process Engineer II, Acquisitions, supporting integration and remediation activities to meet external regulatory standards across Boston Scientific's global plant network.
Key Responsibilities
- Assess process capabilities and implement improvements
- Lead validation/process characterization (TMV, PC, OQ/PQ)
- Contribute to technical reports and qualifications
- Define implementation strategies with P&PC Lead
- Develop and approve technical documentation
Technical Overview
Engineering role focused on validation, process characterization, and design documentation within a regulated medical device framework; requires cross-functional collaboration and knowledge of TMV/OQ/PQ and DFSS tools.
Ideal Candidate
The ideal candidate is a mid-level process engineer with 2+ years of engineering experience, strong Lean/DFM fundamentals, and a background in medical device-like regulated environments, capable of leading validation and cross-functional initiatives during acquisitions.
Must-Have Skills
None listed
Required Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Bachelor's degree in Engineering or related science, Willingness to travel up to 30% (domestic/international)
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