At a Glance
- Tasks: Support quality activities in commercial operations and ensure compliance with regulations.
- Company: Join Johnson & Johnson, a leader in healthcare innovation.
- Benefits: Inclusive work environment, career growth, and competitive benefits.
- Other info: Opportunity to work in a dynamic, multinational environment.
- Why this job: Make a real impact on patient safety and regulatory compliance.
- Qualifications: Bachelor's degree in relevant field and 2-4 years of experience in Quality or Regulatory roles.
The predicted salary is between 35000 - 45000 £ per year.
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.
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.
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.
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.
- 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. Travel: Limited; occasional regional travel within the Netherlands or EU. Certifications: Quality or Regulatory certifications preferred.
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.
CQ Specialist EOV in Leeds employer: 8722-DePuy International Limited Legal Entity
At Johnson & Johnson, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment that fosters personal and professional growth. Our commitment to employee well-being is reflected in our comprehensive benefits package and the opportunity to work at the forefront of healthcare innovation in Leeds, where you can make a meaningful impact on patient safety and regulatory compliance. Join us to be part of a collaborative culture that values diversity and empowers you to contribute to groundbreaking solutions in the medical field.
Contact Details:
8722-DePuy International Limited Legal Entity Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land CQ Specialist EOV in Leeds
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Johnson & Johnson. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Brush up on EU MDR regulations and quality system standards. Show them you’re not just a candidate, but the candidate they need.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources. The more comfortable you are talking about your experience, the better you'll come across.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the team at Johnson & Johnson.
We think you need these skills to ace CQ Specialist EOV in Leeds
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the CQ Specialist EOV role. Highlight relevant experience in quality, regulatory, or compliance roles, especially if you've worked with EU MDR or post-market surveillance activities.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality in healthcare and how your skills align with the responsibilities of the role. Don't forget to mention your understanding of the importance of patient safety!
Showcase Your Attention to Detail:In quality roles, attention to detail is key. Make sure your application is free from typos and errors. You might even want to include examples of how your meticulous nature has positively impacted your previous work.
Apply Through Our Website:We encourage you to apply through our website for the best chance of being noticed. It’s straightforward and ensures your application goes directly to the right team. Plus, you’ll find all the info you need about the role there!
How to prepare for a job interview at 8722-DePuy International Limited Legal Entity
✨Know Your Regulations
Familiarise yourself with the EU MDR and local regulatory requirements. Being able to discuss these in detail will show your understanding of the role and its importance in ensuring patient safety and compliance.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your experience in quality, regulatory, or compliance activities. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.
✨Collaborate Like a Pro
Since this role involves partnering with various teams, be ready to discuss how you've successfully collaborated in the past. Highlight your communication skills and any cross-functional projects you've been part of.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to quality and compliance, especially regarding EOV responsibilities. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
