QA Specialist
3 dni temu
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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
- Full-time
- Quality Assurance
- Pharmaceutical Manufacturing
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