Quality Coordinator

Ferring Pharmaceuticals; Glasgow; On-site; GBP 80,000 - 100,000; Full time

Job summary

A leading pharmaceutical company in Glasgow is seeking a Quality Assurance Coordinator for a 6-month temporary contract. The successful candidate will contribute to site compliance with Good Manufacturing Practices (GMP) and manage the approval of documentation and audits. Ideal candidates should have at least two years of Quality Assurance experience in the pharmaceutical industry. Competitive benefits include a global bonus plan, annual leave, and a flexible working schedule.

Benefits

Ferring Global Bonus Plan

25 days annual leave, plus 9 bank holidays

Employer pension contribution: 7% min

Flexible working schedule

Enhanced Maternity & Paternity Policy

Private medical and dental care scheme

Qualifications

• Minimum of two years experience in Quality Assurance, preferably in the pharmaceutical industry.
• Familiarity with GXP regulations in a highly regulated environment.

Responsibilities

• Review and approve batch records and reports.
• Perform room authorisation checks during manufacturing.
• Monitor manufacturing processes and conduct internal audits.
• Participate in GMP inspections and address compliance issues.

Job description

Job Description: We have an exciting opportunity QA Coordinator to join us on a 6-month temporary contract.

Ferring Controlled Therapeutics is a highly successful pharmaceutical manufacturing, research and development company located in East Kilbride and we are currently seeking a Quality Assurance Coordinator to join our existing team.

Working within the Quality Assurance Department, the successful candidate would contribute to ensuring site compliance with Good Manufacturing Practices (GMP) and manufacturing licences for marketed products and clinical trials.

Reporting to the Quality Assurance Manager this position would ideally suit a Quality Assurance professional with at least five years relevant experience within the pharmaceutical industry or a regulated environment.

Responsibilities and Duties:

• Review and approval of batch records, reports, and other associated documentation
• Perform room authorisation checks during manufacturing and packaging processes
• In process control sampling and tests, monitoring of manufacturing process
• Perform Internal Audits
• Participate in GMP Inspections and audits
• Investigate deviations and CAPA implementation
• Follow up compliance issues in production
• Contribute to Site Quality Objectives and quality improvement projects

Required Experience and Competencies:

• Quality Assurance: 2 years (Preferred)
• Experience in pharmaceutical GXP regulated work or a highly regulated environment is preferred.

What you’ll get in return:

• Ferring Global Bonus Plan
• 25 days’ annual leave, plus 9 bank holidays
• Employer pension contribution: 7% min
• Flexible working schedule
• Enhanced Maternity & Paternity Policy
• Private medical and dental care scheme

About us:

Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group active in global markets. The company identifies, develops, and markets innovative products in the areas of reproductive health, urology, gastroenterology, endocrinology, and orthopaedics. Ferring has its own operating subsidiaries in nearly 60 countries and markets its products in 110 countries. To learn more about Ferring or its products please visit www.ferring.com.

Location: Ferring Controlled Therapeutics UK