Bragg Life Sciences
Quality Control Inspector
Skills
1 month ago
Share this opportunity
Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.
Important information
Contract type:
Permanent
Location:
Glasgow, UK
Work mode:
Onsite
Published on:
8 September 2026
What they need
Our client is a market leader Life Sciences manufacturing products (medicinal, cosmetic and medical device) throughout the UK, Ireland and the Middle East. From their head office in Glasgow, they send products to as many as 60 countries. They are looking to strengthen the QC team by adding a Quality Control Inspector for their site.
The Quality Control Inspector is responsible for the timely sampling, inspection, labelling, documentation and release of raw materials and packaging components in line with procedures, approved specifications, Good Manufacturing Practice (GMP) and applicable quality standards. The role supports production efficiency, inspection readiness and continuous improvement within the Quality Control function.
Responsibilities & Accountabilities:
- Inspect packaging components against approved artwork, specifications and quality requirements
- Sample and label raw materials, inspect deliveries and review containers against approved specifications
- Prepare, review and maintain documentation, including artwork, specifications and Quality Control records
- Manage retained samples for raw materials, contract goods and packaging components
- The Quality Control Inspector will complete inspection and documentation activities promptly, accurately and in line with GMP, hygiene, safety and housekeeping requirements
- Represent Quality Control at product, departmental or company meetings as required
- Support continuous improvement of Quality Control systems and processes.
- Maintain quality standards and assure compliance
- Support production through timely inspection and release activity
- Identify errors early to reduce downtime and improve efficiency
- Maintain inspection readiness across relevant activities and records
Skills & Qualifications:
- Attention to detail with a quality-focused, right-first-time mindset
- Computer literate with good documentation practice
- Knowledge of current GMP and health and safety practices
- Experience in a GMP-compliant environment, preferably Life Sciences
- Experience of, or exposure to, regulatory audits (desirable not a deal breaker)
- HNC or equivalent is desirable, practical expertise also considered
- Driving licence required
Benefits
- Holidays – 33 days per annum
- Private Health Cover
- Company Pension Scheme - doubled company contribution
- Life Assurance Cover of 8 times annual salary
- Company Bonus Scheme
- Virtual GP and Wellbeing Program
- Company Sick Pay
- Free flu vaccine
- Group income Protection – paying 80% of salary for up to 5 years if off for 6 months or more
- Half day finish on a Friday
Working hours
- 37 hours per week
- Monday - Thursday 08:00-16:30
- Friday – 08:00-13:00
Pay: £28,000.00-£32,000.00 per year
Benefits:
- Company pension
- Free flu jabs
- Health & wellbeing programme
- Life insurance
- On-site parking
- Private medical insurance
- Profit sharing
- Sick pay
Work Location: In person
Other offers great for you!
These companies are also looking for great profiles
Alpineo Consulting
Control Engineer - Inverter & Motor Control
Permanent contract
Luxembourg
Onsite
Skills
3 days ago
Quick apply
Naxo
Analyst Data Quality
440
Freelance
Lille, France
Hybrid
Skills
3 days ago
Quick apply
CAPEFRONT Energies
Senior Installation Engineers
Freelance
Lisbon, Portugal
Onsite
Skills
9 hours ago
Quick apply