Packaging & Labelling Engineer in Cirencester

Packaging & Labelling Engineer in Cirencester

Cirencester Full-Time 58000 - 62750 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead projects ensuring compliance and performance of medical device packaging and labelling.
  • Company: Join a leading medical device company focused on innovation and quality.
  • Benefits: Competitive salary, generous holiday, private medical insurance, and career development.
  • Other info: Collaborative team culture with opportunities for mentorship and growth.
  • Why this job: Make a real impact on global health by ensuring the safety of medical devices.
  • Qualifications: Degree in engineering or related field with experience in regulated environments.

The predicted salary is between 58000 - 62750 £ per year.

We are looking for an experienced Senior Packaging & Labelling Engineer to join our Validation & Sterility Assurance team based onsite in Cirencester.

This is a pivotal role responsible for ensuring the compliance, performance, and continuous improvement of our medical device packaging, labelling, and packing systems across a global portfolio.

As the subject matter expert for packaging and labelling validation, you will lead critical projects, support regulatory compliance activities, mentor a small team, and work closely with colleagues across Quality, Regulatory Affairs, R&D, Manufacturing, and external partners.

This is an excellent opportunity for a driven engineer who enjoys technical problem-solving, project leadership, and influencing business-wide quality and compliance strategies within a highly regulated medical device environment.

  • Monitor and validate all aspects of medical device packaging and labelling, including:
  • Transportation testing
  • Shelf-life studies
  • Equipment performance validation
  • Labelling control systems
  • Label content compliance
  • Support a global portfolio of medical devices, including orthopaedic implants, reusable instruments, and single-use devices.
  • Review and approve technical documentation, labels, and packaging Bills of Materials (BOMs).
  • Drive continuous improvement of packaging and labelling validation strategies.

• Manage validation and improvement projects, including

  • Equipment qualification and validation
  • Product evaluations
  • New system implementation
  • Collaborate with cross-functional global teams, including Regulatory Affairs, R&D, Quality, Operations, contractors, and external laboratories.
  • Ensure regulatory compliance deadlines are achieved and maintained and provide technical responses to regulatory authorities.
  • Develop and deliver training to operational teams.
  • Lead investigations relating to non-conformances, CAPAs, and customer complaints.
  • Act as an auditee during internal, customer, and regulatory audits.
  • Mentor, supervise, and develop a small team, including participation in recruitment activities.
    Degree in a scientific, engineering, or related technical discipline.
  • Proven experience within the medical device industry or another highly regulated environment.
  • Strong understanding of packaging and labelling validation requirements.

• Experience working with

  • MDR and/or MDD
  • ASTM standards
  • Knowledge of Good Manufacturing Practice (GMP).
  • Strong analytical, investigative, and problem-solving skills.
  • Excellent attention to detail.
  • Ability to manage multiple priorities and complex technical projects.
  • Strong written and verbal communication skills with the ability to influence stakeholders at all levels.

Desirable

  • Previous experience mentoring, coaching, or supervising others.
  • Experience leading validation projects within a medical device manufacturing environment.
  • Exposure to regulatory inspections and external audits.
  • Experience of packaging equipment validation and qualification.

Why Join Us?

  • Play a key role in ensuring the safety and compliance of innovative medical devices used worldwide.

With the opportunity to Lead impactful projects within a collaborative, cross-functional environment

  • A competitive salary of £58,000 - £62,750 and a discretionary annual bonus
  • 25 days holiday plus bank holidays
  • Excellent pension - starts at 6%, going up to 9.7% after 18 months.
  • Life assurance - Six times your basic salary
  • Private medical insurance with BUPA for you and your family
  • Free annual eye tests and flu vaccinations
  • Employee referral program where you can earn from £1,000 for each successful hire you recommend
  • Opportunity to work on regulated, high-impact medical device products
  • Ongoing professional development and career progression opportunities
  • Be part of a business committed to quality, innovation, and improving patient outcomes.
  • #J-18808-Ljbffr

Packaging & Labelling Engineer in Cirencester employer: CORIN LIMITED

At CORIN LIMITED, we pride ourselves on being an excellent employer, offering a dynamic work culture that fosters collaboration and innovation in the medical device sector. Our Cirencester location provides a supportive environment where you can grow your career through mentorship and continuous improvement initiatives, while also enjoying the benefits of working with a global portfolio of cutting-edge technologies. Join us to make a meaningful impact in healthcare and advance your professional journey in a company that values your contributions.

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Contact Details:

CORIN LIMITED Recruitment Team

We think you need these skills to ace Packaging & Labelling Engineer in Cirencester

Packaging and Labelling Validation
Regulatory Compliance
Project Leadership
Technical Problem-Solving
ISO 13485
ISO 11607
21 CFR 820.75