Quality & Compliance Training Lead
On-site · Manchester, New Hampshire, United States
Manchester, New Hampshire, United StatesOn-siteFull TimeMid LevelAssociates DegreeMedical Device ManufacturingUnknown
Type
Full Time
Level
Mid Level
Education
Associates Degree
Company size
Unknown
Industry
Medical Device Manufacturing
Job Summary
Lead the development and management of the company’s training program within the QMS in compliance with ISO 13485 and FDA QSR; oversee onboarding, role-based qualification, and ongoing compliance training; maintain training records, curricula, and content; generate compliance reports and dashboards; collaborate across Quality, HR, Manufacturing, Engineering, and Regulatory Affairs to ensure workforce competency and training compliance.
Required Qualifications
- 2–5 years of experience in training coordination, quality systems, or regulated industry environment (medical device preferred)
- Experience managing training systems, LMS platforms, or QMS training modules
- Working knowledge of ISO 13485 and FDA QSR requirements related to training and competency
- Instructional design or training development certification is a plus
- ASQ certifications (CQA, CQIA, or similar) are an advantage
- Strong communication and facilitation skills
- Proficiency in Microsoft Office and learning management or QMS systems
Desired Qualifications
- Experience managing training systems, LMS platforms, or QMS training modules
- Strong understanding of ISO 13485 and FDA QSR requirements related to training and competency
- Instructional design or training development certification is a plus
- ASQ certifications (CQA, CQIA, or similar) are an advantage
- Strong communication and facilitation skills
- Proficiency in Microsoft Office and learning management or QMS systems
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