Manufacturing Engineer Grove Technical Resources
- Contractor
Looking for a Manufacturing Transfer Engineer with 5+ years of medical device experience, strong expertise in manufacturing/technology transfers, CMO management, IQ/OQ/PQ validation, Design Transfer, CAPA, FMEA, and FDA/ISO 13485 regulated environments.
Execute manufacturing transfer activities between external Contract Manufacturing Organizations (CMOs).
Develop and maintain transfer plans, project schedules, risk assessments, and execution timelines.
Coordinate technology transfer activities, including manufacturing documentation, work instructions, SOPs, and operator training.
Support duplication and strategic build-up of manufacturing lines across multiple CMOs to improve supply chain resilience and business continuity.
Collaborate with Manufacturing, Quality, Operations, Supply Chain, R&D, Regulatory Affairs, and external manufacturing partners throughout transfer activities.
Support equipment installation, qualification, and process validation activities (IQ, OQ, and PQ).
Execute Design Transfer activities in accordance with Design Control requirements and applicable Quality System regulations.
Prepare and support Engineering Change Orders (ECOs), Change Controls, Deviations, CAPAs, and risk management documentation.
Identify manufacturing risks, troubleshoot transfer issues, and implement effective mitigation plans.
Support process characterization, process optimization, and continuous improvement initiatives.
Monitor project milestones, communicate project status, and escalate risks or issues when necessary.
Ensure compliance with FDA Quality System Regulations, ISO 13485, GMP, and internal quality procedures.
| Location | UT |
| Job Type | Contractor |
Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, Industrial Engineering, or a related engineering discipline.
5+ years of experience in Manufacturing Engineering, Process Engineering, Manufacturing Transfer, Technology Transfer, or New Product Introduction (NPI) within the medical device industry.
Experience supporting manufacturing transfers between internal manufacturing sites and/or external CMOs.
Experience with manufacturing line duplication, production scale-up, or manufacturing expansion projects.
Hands-on experience supporting equipment qualification and process validation (IQ/OQ/PQ).
Working knowledge of Design Transfer, Design Controls, and Engineering Change processes.
Experience with Change Control, CAPA, Deviations, Risk Assessments, and FMEA.
Strong problem-solving, technical documentation, and cross-functional communication skills.


