QA Specialist

3 dni temu


Warszawa, Mazovia, Polska RBW Consulting Pełny etat

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CDMO and Vendor - Delivering recruitment solutions across the UK and Europe.

QA Specialist

Location: Warsaw, Poland

Are you an experienced QA professional with a background in GMP pharmaceuticals? We are looking for two dedicated QA Specialists to join a dedicated QA team in Warsaw. One role will focus on QC documentation, and the other on Quality Management Systems (QMS), with significant interaction with the Berlin site.

Key Responsibilities:

  • QC Documentation Specialist:
  • Manage and maintain quality control documentation.
  • Ensure compliance with GMP standards.
  • Collaborate with the QC team to support documentation needs.
  • QMS Specialist:
  • Oversee and maintain the Quality Management System.
  • Interact frequently with the Berlin site to ensure alignment and compliance.
  • Implement and monitor QMS processes and improvements.
  • Work hours: 7am-3pm, 8am-4pm – changing weekly

Role Requirements:

  • At least 1 year+ of QA experience in a GMP pharmaceutical environment.
  • Strong attention to detail and organizational skills.
  • Excellent communication and collaboration abilities.

What's On Offer:

  • A supportive and dynamic work environment.
  • Opportunities for professional growth and development.
  • Competitive salary and benefits.

If you are ready to take on a challenging and rewarding role in quality assurance, apply now to join this team and contribute to a mission of maintaining the highest standards of quality.

Apply today and be a part of quality assurance excellence

Seniority level
  • Associate
Employment type
  • Full-time
Job function
  • Quality Assurance
  • Pharmaceutical Manufacturing
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