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CQ Specialist EOV

Leeds, West Yorkshire, United KingdomPosted 2 days ago
FULL_TIMEhybrid

Job Description

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 MedTech, 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. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Quality

Job Sub Function:

Customer/Commercial Quality

Job Category:

Professional

All Job Posting Locations:

Amersfoort, Utrecht, Netherlands, Leeds, West Yorkshire, United Kingdom

Job Description:

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.​

DePuy Synthes is recruiting for a(n) Commercial Quality Specialist – EOV, located in Leeds, West Yorkshire, United Kingdom.

ob Overview 

The Commercial Quality Specialist – EOV supports quality activities related to commercial operations within the Netherlands market, with a focus on EOV (Economic Operators & Vigilance) responsibilities. This role helps ensure compliance with EU MDR, local regulatory requirements, and internal quality system standards across distribution and post‑market activities. The position plays an important role in safeguarding patient safety, maintaining regulatory compliance, and supporting business continuity by partnering closely with Commercial, Regulatory Affairs, and Supply Chain teams. 

 

Key Responsibilities 

  • Support commercial quality activities related to EOV obligations, ensuring compliance with EU MDR, local regulations, and internal quality policies. 

  • Support post‑market surveillance and vigilance activities, including complaint handling, incident reporting, and field action support. 

  • Assist with implementation and maintenance of quality system processes related to commercial operations and EOV responsibilities. 

  • Partner with Commercial, Regulatory Affairs, and Supply Chain teams to support compliant product distribution and lifecycle activities. 

  • Participate in internal audits, external audits, and health authority inspections as required. 

  • Monitor quality issues, trends, and metrics related to EOV and post‑market activities and support corrective and preventive actions. 

  • Maintain accurate quality documentation, records, and reports related to commercial quality and EOV activities. 

  • Contribute to continuous improvement initiatives to strengthen quality compliance and operational effectiveness. 

 

Qualifications 

Education: 

  • Bachelor’s degree in Quality, Engineering, Life Sciences, Regulatory Affairs, or a related discipline (required). 

  • Advanced degree in a scientific, quality, or regulatory field (preferred). 

Experience and Skills: 

Required: 

  • Typically 2-4 years of experience in Quality, Regulatory, or Compliance roles within a regulated industry. 

  • Experience supporting EOV, vigilance, or post‑market surveillance activities. 

  • Foundational understanding of EU MDR and quality system requirements for commercial operations. 

  • Experience supporting audits, inspections, or regulatory reporting activities. 

Preferred: 

  • Experience in medical devices, healthcare, or other highly regulated industries. 

  • Familiarity with Dutch regulatory requirements and EU health authority interactions. 

  • Experience working in a multinational or matrixed organization. 

  • Exposure to notified body or competent authority inspections. 

  • Quality or Regulatory certifications (e.g., RAC, ASQ). 

  • Strong attention to detail, documentation, and organizational skills. 

  • Effective communication and cross‑functional collaboration skills. 

Other: 

  • Language: English required. 

  • Travel: Limited; occasional regional travel within the Netherlands or EU. 

  • Certifications: Quality or Regulatory certifications preferred but not required. 

 

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com. 

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. 

  

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. 

  

#LI-Hybrid 

#DePuySynthesCareers 

 

 

Required Skills:

 

 

Preferred Skills:

Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment
CQ Specialist EOV at Jj | Renata