DePuy Synthes is recruiting for a(n) EMEA CQSS Specialist,locatedin LSt Anthony's Road, Leeds, UK Alternate Hybrid locations may be considered at Umkirch, Germany, Loughbeg, Ringaskiddy, Zug, Switzerland

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):

Loughbeg, Ringaskiddy Ireland and Umkirch, Germany - Requisition Number: R-082530

Zug, Switzerland - Requisition Number: 082534

Johnson & Johnson announced plans to separate our Orthopedics business toestablisha standalone orthopedics company, operating as DePuy Synthes. The process of the planned separation isanticipatedto be completed within 18 to24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may berequired, regulatory approvals and other customary conditions and approvals. Should you accept this position, it isanticipatedthat, following conclusion of the transaction, you would be an employee of DePuySynthesand 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 atan appropriate timeand subject to any necessary consultation processes.

The EMEA CQSS Specialist supports the execution and continuous improvement of regionalCommercialQuality and Safety Surveillance (CQSS) activities across the EMEA region. This role plays a critical part in ensuring compliance with applicable quality system requirements, supportingpost‑marketsurveillance and vigilance processes, and partneringcross‑functionallytomaintainpatient safety and regulatory readiness. This is an opportunity to contribute directly to product quality, regulatory compliance, and patient outcomes within a leadingorthopedicsorganization.

Key Responsibilities

• Support EMEA CQSS activities, includingpost‑marketsurveillance, quality system compliance, and safety reporting processes in alignment with global and regional requirements.

• Assistin 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 withcross‑functionalpartners (e.g., Regulatory Affairs, Medical Safety, Operations) to supporttimelyinvestigation and resolution of quality and compliance issues.

• Contribute to continuous improvement initiatives byidentifyingopportunities to enhance CQSS processes, tools, and reporting.

• Maintainaccuratetracking and reporting of CQSS metrics to support management review and regulatory compliance.

Qualifications

Education

• Bachelor’s degreerequiredin 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‑marketsurveillance, vigilance).

• Experience supporting investigations, documentation, and quality recordsin accordance withestablished procedures.

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

Preferred:

• Experience supportingEMEA‑basedquality, vigilance, or regulatory activities within the medical device industry.

• Familiarity with EU MDR/IVDRpost‑marketsurveillance and safety reporting requirements.

• Experienceparticipatingin audits or health authority inspections.

• Proficiencywith quality systems, databases, and reporting tools.

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

Other:

• Languages:Proficiencyin Englishrequired;additionalEMEA language skills are a plus.

• Travel: Limited regional travel may berequired(generally upto 10%).

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

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