Are you ready to take your career in Quality Control to the next level? Do you have a passion for ensuring the highest standards of raw materials in the pharmaceutical or biotech industry? If so, this is your opportunity to shine!

Your role would be to:

• Manage tasks related to the sampling of raw materials, excipients, clean media (water, gases), and single-use materials.
• Evaluate reports from external laboratories and perform physicochemical testing of media.
• Develop and review specifications, procedures, and instructions related to raw materials.
• Support the release process of starting materials by verifying release documentation and preparing certificates of analysis.
• Maintain accurate documentation in line with GMP and regulatory requirements.
• Participate in supplier qualification and requalification processes.
• Monitor and report the condition of control and measuring equipment.
• Play an active role in audits, risk assessments, and change control processes.
• Drive improvements in GMP compliance, process efficiency, and workplace safety.

Our expectations:

• Higher education in biotechnology, chemistry, or related).
• Over 3 years of experience in Quality Control or a similar role.
• Good working knowledge of GMP, EMA, FDA regulations, pharmacopoeial guidelines, and pharmaceutical law.
• Fluency in English (oral and written).
• Proficiency in MS Office.
• Strong organizational and multitasking abilities.
• Clear communication and reporting skills.

What We Offer:

• Employment at a company that is a leader in the Polish biotechnology sector, and contribute to life-changing medicines reaching patients globally.
• Collaboration with experts from the world’s leading biotechnology companies.
• Attractive benefits package, including:
  
  • Private healthcare.
  • Life insurance.
  • Employee Pension Program (EPP).
  • Annual and occasional bonuses.
  • Financial support for skills development.
  • Lunch card.
  • One additional day off per year (Polpharma Day).
• And much more...