Sr Compliance Specialist, Rd

Johnson & Johnson

Jacksonville, Florida, United States of America
Onsite
Fda/gmp and iso regulations
Non-conformance resolution process
Internal assessments and quality trends
The Sr Compliance Specialist, R&D is primarily responsible for ensuring that the laboratories operate in compliance with FDA/GMP and ISO regulations

Job Summary

  • The Sr Compliance Specialist, R&D is primarily responsible for ensuring that the laboratories operate in compliance with FDA/GMP and ISO regulations.
  • This role facilitates the departmental non-conformance resolution process, performs internal assessments, analyzes quality/compliance trends and reports conclusions.
  • You will be responsible for ensuring departmental compliance to FDA/GMP and ISO regulations, including the facilitation of the non-conformance resolution process and performing internal assessments.

Matching Summary

The Sr Compliance Specialist, R&D is primarily responsible for ensuring that the laboratories operate in compliance with FDA/GMP and ISO regulations.

Skills & Requirements

Must-have

  • FDA/GMP and ISO regulations
  • Non-conformance resolution process
  • Internal assessments and quality trends
  • Departmental quality policies and procedures
  • Laboratory equipment and systems compliance

Nice-to-have

  • Passion for vision treatment innovation
  • Collaborative problem-solving
  • Leadership in quality compliance

Key Requirements

  • Bachelor's degree in a technical field
  • 4+ years regulated industry experience
  • Certified Quality Auditor (CQA) certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter