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Senior Source Regulatory Compliance Specialist

Job in Leeds, West Yorkshire, ME17, England, UK
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-05-31
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 60000 - 80000 GBP Yearly GBP 60000.00 80000.00 YEAR
Job Description & How to Apply Below

About Johnson & Johnson

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Job

Function

Quality

Job Sub Function

Quality & Compliance Audit

Job Category

Professional

Location

Leeds, West Yorkshire, United Kingdom

Job Overview

The Sr. Source Regulatory Compliance Specialist is responsible for executing and supporting regulatory compliance activities related to sourcing, suppliers, and externally provided processes. This role ensures that suppliers, contract manufacturers, and sourced materials comply with applicable regulatory requirements, quality system standards, and internal policies. The position has a direct impact on product quality, audit readiness, and supply continuity by partnering closely with Quality, Regulatory Affairs, Supply Chain, and Procurement teams across the region.

Key Responsibilities
  • Execute source regulatory compliance activities including supplier audit execution, investigation approval, and objective evidence review, to ensure adherence to regulatory and quality system requirements.
  • Support compliance oversight for suppliers, contract manufacturers, and externally provided services.
  • Partner with Supply Chain, Procurement, Quality, and Regulatory Affairs teams to support compliant supplier qualification and lifecycle management.
  • Interpret regulatory requirements and support translation into sourcing and supplier compliance expectations.
  • Support internal audits, external audits, and health authority inspections related to sourcing and supplier compliance.
  • Monitor compliance risks, trends, and supplier performance metrics; support corrective and preventive actions.
  • Ensure accurate maintenance of compliance documentation, records, and reports.
  • Contribute to continuous improvement initiatives to strengthen supplier compliance governance and effectiveness.
Qualifications Education
  • Bachelor’s degree in Regulatory Affairs, Quality, Engineering, Life Sciences, Supply Chain, or a related discipline (required).
  • Advanced degree in a scientific or regulatory field (preferred).
Experience and Skills Required
  • Typically 4-6 years of experience in Regulatory Compliance, Quality, Supply Chain, or related roles within a regulated industry.
  • Working knowledge of regulatory and quality requirements impacting sourcing and supplier operations.
  • Experience leading supplier audits, inspections, or compliance assessments.
  • Ability to manage complex compliance topics and documentation with strong attention to detail.
  • Strong analytical, organizational, and problem‑solving skills.
  • Effective written and verbal communication skills.
Preferred
  • Experience in medical devices, healthcare, or other highly regulated industries.
  • Familiarity with global regulatory and supplier compliance expectations.
  • Experience working in a global or matrixed organization.
  • Exposure to regulatory inspections involving supplier or contract manufacturing oversight.
  • Quality or Regulatory certifications (e.g., RAC, ASQ).
Other
  • Language:
    English required, additional European language preferred.
  • Travel: moderate regional; limited international travel.

Johnson & Johnson is an equal opportunity employer. The process of the planned separation of our Orthopaedics business is anticipated to be completed within 18 to 24 months. Should you accept this position, it is anticipated that you would be an employee of DePuy Synthes.

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Position Requirements
10+ Years work experience
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