Senior Supplier Quality Engineer – MedTech Quality

Brighter Signals

Florida

Sur place

USD 79 000 - 128 000

Plein temps

Il y a 5 jours
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Avantages offerts par ce poste

Comprehensive benefits
Long-term incentive program
Vacation leave 120 hours/year

Résumé du poste

Johnson & Johnson's DePuy Synthes division in Palm Beach Gardens, FL, is seeking a Sr. Supplier Quality Engineer to lead quality assurance across contract manufacturers and raw material suppliers.

You will implement SQ strategies, manage non-conformities, CAPA, supplier changes, and support inspections while working with Quality, Engineering, Regulatory and Sourcing teams.

Strong background in GMP/ISO, root-cause analysis, and Six Sigma is preferred; up to 10% travel may be required.

Qualifications

  • Bachelor's or equivalent university degree is required; a concentration in Engineering, Life Science, or related field is preferred.
  • A minimum of 2–4 years of experience in a GMP and/or ISO regulated industry is required.
  • Strong communication, teamwork, and problem-solving skills are essential.
  • Ability to work in a fast-paced environment and collaborate across functions.

Responsabilités

  • Implement SQ strategy and follow Supplier Quality standards.
  • Manage supplier-related non-conformities and CAPA.
  • Oversee supplier change requests and support process validations at suppliers.
  • Provide quality engineering support for PLM changes and supplier QMS activities.
  • Coordinate supplier readiness for inspections by authorities and third parties.
  • Report on supplier performance and participate in management reviews.

Connaissances

Communication
Teamwork
Problem solving
Root cause analysis
Analytical thinking
Learning agility

Formation

Bachelor's degree

Description du poste

Johnson & Johnson's DePuy Synthes division in Palm Beach Gardens, FL, is seeking a Sr. Supplier Quality Engineer to lead quality assurance across contract manufacturers and raw material suppliers.

You will implement SQ strategies, manage non-conformities, CAPA, supplier changes, and support inspections while working with Quality, Engineering, Regulatory and Sourcing teams.

Strong background in GMP/ISO, root-cause analysis, and Six Sigma is preferred; up to 10% travel may be required.

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