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Quality Specialist II

Job in Bathgate, West Lothian, EH48, Scotland, UK
Listing for: Catalent
Full Time position
Listed on 2026-05-31
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 60000 - 80000 GBP Yearly GBP 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Location

Bathgate, UK

Position Summary

Onsite role, Monday – Friday 37.5 hours per week. As a Quality Specialist II you will support the site’s Quality (GMP) objectives and policies, ensuring quality systems and processes operate to the required standards. You will provide QA expertise across packaging and materials operations, working closely with cross‑functional teams to ensure compliance with GMP, pharmacopoeia, client, and regulatory requirements.

The Role
  • Managing the movement, control, and tracking of GMP documentation to support production schedules
  • Reviewing and approving material specifications, incoming bulk, intermediate and finished materials
  • Reviewing and approving GMP documentation, deviations, and observation reports
  • Performing internal audits, monitoring and trending audit findings
  • Conducting QC inspections and sampling of products and materials
  • Performing receipt inspection and approval of blank label stock
  • Taking and controlling reference samples for packaging components, pre‑printed materials, and devices
  • Approving or rejecting packaging components, pre‑printed materials, and medical devices
  • Creating material specifications for in‑process visual inspections where required
  • Supporting additional quality checks requested by clients, QA, or Operations
  • Verifying shipments against client documentation and approved specifications
  • Recording, communicating, and closing supplier issues, including CAPAs and effectiveness checks, in a timely manner
The Candidate
  • BSc in a relevant scientific discipline or equivalent experience within a pharmaceutical environment or equivalent technical knowledge
  • Experience working within Quality Assurance either Pharmaceutical or Clinical Trials
  • Excellent verbal and written communication skills
  • High level of attention to detail and concentration
  • Strong analytical and problem‑solving skills
Equal Opportunity Statement

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

Disability Accommodation

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to Disabili This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration to the application or hiring process.

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