Supplier Quality Auditor

Gsccareers

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 significantly contributes to the assurance that material and service suppliers to GSK’s manufacturing and supply-chain sites are in adequate compliance with GSK requirements and all applicable standards

Job Summary

  • The role significantly contributes to the assurance that material and service suppliers to GSK’s manufacturing and supply-chain sites are in adequate compliance with GSK requirements and all applicable standards.
  • Day-to-day, the successful candidate will be generally focused on planning, executing and documenting GMP and Quality Systems compliance audits/assessments for a number of assigned suppliers in region and managing associated supplier action plans.
  • The annual base salary in Poland for new hires in this position ranges from PLN 182,250 to PLN 303,750 gross.

Matching Summary

The role significantly contributes to the assurance that material and service suppliers to GSK’s manufacturing and supply-chain sites are in adequate compliance with GSK requirements and all applicable standards.

Salary

Base: PLN 182,250 to PLN 303,750 gross (Poland); Bonus/Equity: potential bonus and/or awards for exceptional performance; Benefits: statutory benefits in accordance with Polish law, private healthcare, additional paid days off, life insurance, private pension plan, fully paid parental leave & care of family member leave

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

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 (QMS)
  • Comfortable with verbal and written English
  • Experience in API, sterile, parenteral, and/or biopharmaceutical manufacturing

Work Rights

Not specified

Tailored Resume

Cover Letter