Specjalista Zapewnienia Jakości/ Specjalistka Zapewnienia Jakości

Polpharma Group

Competitive base salary; performance-based bonus s...
Gmp documentation verification
Deviation management processes
Change control procedures
The role involves evaluating batch reports and verifying GMP documentation for non-sterile solid dosage forms

Job Summary

  • The role involves evaluating batch reports and verifying GMP documentation for non-sterile solid dosage forms.
  • Candidates will manage quality deviations, oversee change controls, and lead CAPA processes within the pharmaceutical sector.
  • The company offers competitive base pay, a bonus system, hybrid work options, and comprehensive benefits including private healthcare.

Matching Summary

The role involves evaluating batch reports and verifying GMP documentation for non-sterile solid dosage forms.

Salary

Competitive base salary; Performance-based bonus system; Not specified

Skills & Requirements

Must-have

  • GMP documentation verification
  • Deviation management processes
  • Change control procedures
  • CAPA process execution
  • Quality agreement drafting
  • Internal and external audits

Nice-to-have

  • Hybrid work environment
  • Team collaboration skills
  • Ability to work under pressure
  • High attention to detail
  • Independent work organization

Key Requirements

  • Master's degree in relevant life science field
  • Minimum 2 years experience in Quality Assurance or Control
  • Fluent English communication skills
  • Proficiency with MS Office and QMS systems like TrackWise
  • Knowledge of pharmaceutical manufacturing technologies

Work Rights

Not specified

Tailored Resume

Cover Letter