Transportation & Temp Control - EMEA

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Job Function:

Quality

Job Sub Function:

Customer/Commercial Quality

Job Category:

Professional

All Job Posting Locations:

Leeds, West Yorkshire, United Kingdom

Job Description:

DePuy Synthes is recruiting for a   Transportation & Temp Control - EMEA ,   located   in Leeds, West Yorkshire, United Kingdom or Ringaskiddy, Ireland or Zug, Switzerland or Umkirch, Germany.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

St. Anthony's Road, Leeds, UK - Requisition Number: R-084917

Loughbeg, Ringaskiddy or Umkirch, Germany - Requisition Number: R-087017

Zug, Switzerland - Requisition Number: R-087019

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

The   Transportation & Temp Control - EMEA   supports the execution and continuous improvement of regional   Commercial   Quality and Safety Surveillance (CQSS) activities across the EMEA region. This role plays a critical part in ensuring compliance with applicable quality system requirements, supporting   post ‑ market   surveillance and vigilance processes, and partnering   cross ‑ functionally   to   maintain   patient safety and regulatory readiness. This is an opportunity to contribute directly to product quality, regulatory compliance, and patient outcomes within a leading   orthopedics   organization.

Key Responsibilities

Support EMEA CQSS activities, including   post ‑ market   surveillance, quality system compliance, and safety reporting processes in alignment with global and regional requirements.

Assist   in the execution and maintenance of quality system documentation, including procedures, work instructions, and records related to CQSS activities.

Participate in complaint handling, vigilance, and trend analysis activities to support identification and escalation of quality and safety issues.

Support internal and external audits, inspections, and regulatory inquiries by preparing documentation and responding to information requests.

Collaborate with   cross ‑ functional   partners (e.g., Regulatory Affairs, Medical Safety, Operations) to support   timely   investigation and resolution of quality and compliance issues.

Contribute to continuous improvement initiatives by   identifying   opportunities to enhance CQSS processes, tools, and reporting.

Maintain   accurate   tracking and reporting of CQSS metrics to support management review and regulatory compliance.

Qualifications

Education

Bachelor’s degree   required   in a scientific, engineering, healthcare, or related discipline.

Advanced degree in Quality, Regulatory, Life Sciences, or a related field preferred.

Experience and Skills

Required:

Typically requires 2–4 years of relevant work experience in Quality, Compliance, Regulatory Affairs, or a related function within a regulated industry (e.g., medical devices, pharmaceuticals).

Working knowledge of quality systems and compliance requirements (e.g., ISO 13485,   post ‑ market   surveillance, vigilance).

Experience supporting investigations, documentation, and quality records   in accordance with   established procedures.

Strong attention to detail with the ability to manage multiple priorities in a regulated environment.

Preferred:

Experience supporting   EMEA ‑ based   quality, vigilance, or regulatory activities within the medical device industry.

Familiarity with EU MDR/IVDR   post ‑ market   surveillance and safety reporting requirements.

Experience   participating   in audits or health authority inspections.

Proficiency   with quality systems, databases, and reporting tools.

Effective written and verbal communication skills, with the ability to collaborate across functions and regions.

Other:

Languages:   Proficiency   in English   required ;   additional   EMEA language skills are a plus.

Travel: Limited regional travel may be   required   ( generally up   to 10%).

Certifications: Quality or Regulatory certifications (e.g., ASQ, ISO Lead Auditor) 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 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.

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.

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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