at PwC
Big FourPosted 11 days ago
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**Manufacturing QMS Consultant (Pharma/Life Sciences & Med Device) - Director** Drive QMS improvements in Pharma, Life Sciences, and Medical Device sectors. Direct cross-functional teams, implement ISO 13485/21 CFR Part 820, ensure compliance, and optimize processes. Requires 10+ years in relevant industry, proven QMS expertise, and leadership experience. Familiarity with IQ/ERP systems and FDA regulations paramount.
- Compensation
- Not specified
- City
- New York City
- Country
- United States
Currency: Not specified
Full Job Description
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