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Quality Control Inspector

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Quality Control Inspector

Bragg Life Sciences

Quality Control Inspector

Skills

Compliance

1 month ago

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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

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