Quality Specialist Ii

Catalent

Bathgate, UK
Onsite
Gmp documentation management
Material specification review
Internal audit execution
Catalent is seeking a Quality Specialist II for their Bathgate, UK location. The role involves ensuring compliance with GMP standards and supporting quality systems in packaging and materials operations

Job Summary

  • The role involves supporting site Quality objectives by ensuring systems operate to required GMP standards.
  • Candidates will manage the movement, control, and tracking of GMP documentation while reviewing material specifications for compliance.
  • Catalent is a global drug development leader producing over 70 billion doses annually to advance life-saving medicines.

Matching Summary

Match Score: 85

Catalent is seeking a Quality Specialist II for their Bathgate, UK location. The role involves ensuring compliance with GMP standards and supporting quality systems in packaging and materials operations.

Skills & Requirements

Must-have

  • GMP documentation management
  • Material specification review
  • Internal audit execution
  • Deviation report analysis
  • CAPA implementation

Nice-to-have

  • Cross-functional team collaboration
  • Strong analytical problem-solving
  • Client quality check support

Key Requirements

  • BSc in relevant scientific discipline
  • Experience in Pharmaceutical Quality Assurance
  • Clinical Trials experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter