Manager, Manufacturing Quality / Quality Manager, Medical Device Manufacturing
Parsippany and Budd Lake, NJ (hybrid) · Hybrid · Full-time
My client needs a hands-on quality leader to own the manufacturing quality system at their medical device site in Northern New Jersey. You'll make Quality part of daily manufacturing decisions instead of inspected in after the fact.
Why you should apply
Serve as the site's Quality Management Representative and Deputy Management Representative for North America
A seat on the site leadership team
Hybrid schedule
Medical, dental, vision, FSA, 401k, PTO, life and disability insurance, and a comprehensive leave program
What you'll be doing
Lead, coach, and develop the Quality team
Own floor presence, disposition decisions, and final product release
Own the CAPA system and lead nonconformance, deviation, and complaint investigations
Drive supplier quality and internal audits
Keep the site ready for customer, certification, and regulatory inspections
About you
Be able to do the job as described.
Working knowledge of ISO 13485, FDA 21 CFR 820 (QMSR), and ISO 14971, applied on the manufacturing floor
Medical device manufacturing background
Able to travel 10%, domestically and possibly internationally
How to apply
We'd love to see your resume, but we don't need it to have a conversation. Email Santiago St. James at sjames@jacobsmgt.com and tell me why you're interested. Or, if you do have a resume ready, apply here.
Numbers & Facts
Location
Parsippany, NJ
Skills
Coachingunmatched
Code of Federal Regulationsunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
FDA (Food and Drug Administration)unmatched
ISO (International Organization for Standardization)unmatched
Insuranceunmatched
Internal Auditunmatched
Leadershipunmatched
Manufacturingunmatched
Manufacturing Managementunmatched
Manufacturing Systemsunmatched
Medical Equipmentunmatched
Quality Managementunmatched
Regulationsunmatched
Vendor/Supplier Evaluationunmatched
Willing to Travelunmatched
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