Supplier Quality Auditor

gssi.world

Ware, UK
Base: pln 182,250 to pln 303,750 gross (pol + ); b...
Fully remote
Gmp assessment of quality critical materials
Planning, executing and documenting audits
Managing supplier action plans
The role supports the Central Supplier Quality Audit and Compliance function for the Pharma Supply Chain, promoting quality and compliance throughout the product life-cycle

Job Summary

  • The role supports the Central Supplier Quality Audit and Compliance function for the Pharma Supply Chain, promoting quality and compliance throughout the product life-cycle.
  • Key responsibilities include planning, executing, and documenting GMP and Quality Systems compliance audits for assigned suppliers, and managing associated corrective action plans.
  • The position requires a confident, self-motivated individual with strong auditing experience and the ability to work remotely as part of a matrix organization, with approximately 30% to 50% travel.

Matching Summary

The role supports the Central Supplier Quality Audit and Compliance function for the Pharma Supply Chain, promoting quality and compliance throughout the product life-cycle.

Salary

Base: PLN 182,250 to PLN 303,750 gross (Poland); Bonus/Equity: Eligible for bonus (if applicable); Benefits: Statutory benefits, private healthcare, additional paid days off, life insurance, private pension plan, fully paid parental leave (Poland)

Skills & Requirements

Must-have

  • GMP assessment of quality critical materials
  • planning, executing and documenting audits
  • managing supplier action plans
  • risk-based recommendation on supplier approval
  • collating identified risks and escalating issues
  • English written and verbal communication

Nice-to-have

  • strong people skills
  • continuous improvement mindset
  • curious and able to assimilate information
  • agile working culture

Key Requirements

  • Relevant experience in a highly regulated environment
  • Degree in Life Science or relevant disciplines
  • Knowledge of current GMP requirements
  • Knowledge of Quality Management Systems principles
  • Experience in API, sterile, parenteral, or biopharmaceutical manufacturing (preferred)
  • Auditor certification (preferred)

Work Rights

Not specified

Tailored Resume

Cover Letter