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QC Inspector

Job in Motherwell, North Lanarkshire, ML1, Scotland, UK
Listing for: Bragg Life Sciences Ltd
Full Time position
Listed on 2026-10-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA
Job Description & How to Apply Below
Our client is a market leader in consumer health products (medicinal, cosmetic and medical device) throughout the UK, Ireland and the Middle East. From their head office in Glasgow, they manufacture products to as many as 60 countries. They are looking to strengthen the QC team by adding a Quality Control Inspector to their operations.

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 license
On offer is the opportunity to join a growing life science company, offering opportunities for development and a half day on Fridays!
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