Supervisor, Quality Assurance Internal Operations

PCI Pharma Services

Cgmp manufacturing operations support
Qa scheduling and project management
Quality system events oversight
This role is responsible for leading QA Associates to ensure compliance with cGMP principles during the manufacturing of clinical and commercial drug products

Job Summary

  • This role is responsible for leading QA Associates to ensure compliance with cGMP principles during the manufacturing of clinical and commercial drug products.
  • The supervisor will partner with Manufacturing Operations, Facilities, and Materials Management to identify and resolve quality issues in a timely manner.
  • Candidates must have a BS degree in a scientific discipline and at least 5 years of relevant GMP experience to qualify for this position.

Matching Summary

This role is responsible for leading QA Associates to ensure compliance with cGMP principles during the manufacturing of clinical and commercial drug products.

Skills & Requirements

Must-have

  • cGMP manufacturing operations support
  • QA scheduling and project management
  • Quality System Events oversight
  • Standard Operating Procedure writing
  • Cross-functional team collaboration

Nice-to-have

  • Previous supervisory experience preferred
  • Experience supporting manufacturing training
  • Knowledge of FDA/ISO regulatory trends
  • Strong interpersonal leadership skills
  • Ability to work overtime or weekends

Key Requirements

  • BS degree in a scientific discipline
  • Minimum 5+ years relevant GMP experience
  • Knowledge of FDA/ISO regulatory requirements
  • Microsoft Office and Windows computer knowledge

Work Rights

Not specified

Tailored Resume

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