At a Glance
- Tasks: Ensure quality compliance and support documentation in a dynamic healthcare environment.
- Company: Join Johnson & Johnson, a leader in healthcare innovation and MedTech.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Exciting career path with potential to join the new DePuy Synthes company.
- Why this job: Make a real impact on health solutions while working with a passionate team.
- Qualifications: 1-2 years in Quality or Regulatory roles, strong attention to detail.
The predicted salary is between 38250 - 46750 £ 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 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.
Learn more at jnj. com.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as De Puy 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 De Puy Synthes and your employment would be governed by De Puy Synthes employment processes, programs, policies, and benefit plans.
In that case, details of any planned changes would be provided to you by De Puy Synthes at an appropriate time and subject to any necessary consultation processes.
All Job Posting Locations: Leeds, West Yorkshire, United Kingdom
Key Responsibilities
- Ensure compliance to all applicable quality standards & regulatory requirements in the UK/Ireland LOCs and JJMS.
- Support documentation of the Quality Management System (QMS) processes in the document management system and assist other departments to ensure documents are maintained.
- Support training activities – including maintenance & implementation of the training matrix, development and issuance of training metrics on a regular basis.
- Own, track and conduct non-conformances and CAPA investigations and document in the appropriate systems using approved tools.
- Ability to work alone but part of a virtual team. Work independently to resolve quality issues locally or where applicable with appropriate escalation.
- Manage & lead change control activities as applicable.
- Support Monthly metric generation & collate data for Quality Management Review.
- Act as records coordinator for UK / Irl LOC.
- Assist in driving continuous improvements, simplification & standardization within the QMS.
- Execute a culture of compliance and good customer service/feedback.
- Ensure compliance with the procedures and processes.
- Support & Participate on site audits (e. g. from regulatory bodies).
- Collaborate closely with Sales, Customer Service, and Distribution/Returns teams.
- Required Experience
1-2 years' experience in Quality, Regulatory, or Compliance within a regulated environment.
Understanding of quality systems and regulatory requirements.
Strong attention to detail and documentation skills.
Excellent written and verbal English communication.
Ability to work independently and cross-functionally.
Strong computer skills (Excel, Word, Power Point, Outlook, and business systems).
Customer-focused with strong relationship-building skills.
Preferred Experience
Medical devices, healthcare, pharmaceuticals, or other regulated industries.
Audit, inspection, or regulatory assessment support.
Experience in a multinational or matrix organization.
Exposure to health authority or notified body inspections.
Ideal Candidate Profile
This role would suit someone with early-career quality or regulatory experience who enjoys: Investigating issues and solving problems.
Working with compliance processes.
Collaborating with multiple stakeholders while maintaining high attention to detail.
- Required Skills
- None
- Preferred Skills
- Business Behavior
- Compliance Management
- Continuous Improvement
- Data Analysis
- Data Compilation
- Detail-Oriented
- Execution Focus
- Goal Attainment
- Internal Controls
- Issue Escalation
- Process Oriented
- Quality Control (QC)
- Quality Management Systems (QMS)
- Quality Standards
- Regulatory Environment
- Report Writing
- #J-18808-Ljbffr
Commercial Quality Specialist | Johnson & Johnson| MedTech employer: 7355-Johnson & Johnson Medical Limited Legal Entity
At Johnson & Johnson Medical Limited, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. Our Global Value Creation Lead role offers not only competitive benefits and opportunities for professional growth but also the chance to work in a dynamic environment that values accountability and stakeholder engagement. With significant international travel and the ability to shape impactful solutions, this position is perfect for those seeking meaningful and rewarding employment.
Contact Details:
7355-Johnson & Johnson Medical Limited Legal Entity Recruitment Team
