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Salary
$40k – $49k per year
Location
In office (Cirencester)
Visa
Licensed UK visa sponsor

Confirmed on the employer's own hiring board on Oct 13, 2026. First seen by Alion on Sep 14, 2026. Corin Group info@coringroup scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Discover Corin’s innovative orthopaedic technology that’s revolutionizing patient care with advanced implants and robotic surgery solutions.

Packaging and Labelling Engineer

Corin are looking for a Packaging and Labelling Engineer to join our team and play a key role in ensuring all packaging and labelling activities meet the required regulatory standards for medical devices. This is an excellent opportunity for an experienced engineer with a strong compliance mindset who enjoys ownership, technical challenge, and cross-functional collaboration.

What you’ll do

Validating equipment used in the packaging and labelling of medical devices to the required regulatory standards

Providing technical support and coordinating packaging and labelling activities for new products, including project management of validation, transit testing and shelf-life testing

Writing and executing validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and Process Validation, with hands-on testing and coordination of activities

Creating and maintaining medical device labels and Packaging Bills of Materials (PBOMs)

Managing and administering the label database and label management software

Coordinating and managing requests for PBOM-related translations, including labels and Instructions for Use (IFUs)

Owning packaging and labelling systems, identifying opportunities for improvement and implementing enhanced processes and packaging solutions

Working in compliance with cGMP requirements and industry best practice

Supporting New Product Introduction (NPI/PCT) project requirements and communicating progress at team meetings

Ensuring compliance with relevant packaging, labelling and validation standards, including:

21 CFR 820.75

ISO 13485

ASTM standards

ISO 19227, ISO 14644, ISO 11137, ISO 11135, ISO 11607

 

About You

Practical experience within the medical device industry (preferred), with manufacturing environment experience being highly beneficial

Strong analytical and problem-solving skills

Excellent written and verbal communication skills

The ability to work independently with minimal supervision

Confidence working within multi-disciplinary teams while managing multiple priorities effectively

What We Offer

A competitive salary from £30,000 - £37,000 depending on experience and a discretionary annual bonus of 7.5%

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 up to £1,000 for each successful hire you recommend

Opportunity to work on regulated, high-impact medical device products

A collaborative, quality-driven working environment

Ongoing professional development and career progression opportunities

How to Apply

If you are a detail-focused engineer with a passion for regulatory compliance and continuous improvement, we’d love to hear from you. Please apply with your CV or contact us for further information.

 

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