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Sr. QA/GCP specialist/manager Amsterdam • QTC Recruitment
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Gevraagd
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40 uur
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Medior/Senior
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Engels (taal)
Aanbod
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Vast contract
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Bonusregeling, Pensioenregeling
Vacature in het kort
Amsterdam
Join a leading biotechnology company dedicated to advancing life sciences through innovation and research. As a Senior QA/GCP Specialist/Manager, you will play a crucial role in ensuring top-tier quality standards in clinical operations. Lead compliance efforts, develop quality management systems, and collaborate with cross-functional teams. Discover more about this exciting opportunity by reading further.
Over het bedrijf
QTC Recruitment
Werving en selectie
Bedrijfsprofiel
Volledige vacaturetekst
Our client is a leading biotechnology company committed to advancing life sciences through innovation and high-quality research. Their solutions drive progress in clinical development, regulatory compliance, and patient safety, supporting breakthroughs across the industry. As the company continues to grow, they are expanding their team and are currently seeking a Senior QA/GCP Specialist/Manager to oversee quality assurance in clinical operations.
This is how you will make the difference
As a Senior QA/GCP Specialist/Manager, you will ensure the highest quality standards in clinical operations, leading compliance efforts and ensuring alignment with regulatory and industry requirements. You’ll develop and maintain quality management systems, oversee audits, and support clinical teams in adhering to Good Clinical Practice (GCP) guidelines. Your role involves identifying and addressing compliance risks, implementing corrective and preventive actions, and ensuring inspection readiness. You’ll collaborate with cross-functional teams, including clinical operations and regulatory affairs, to uphold quality across all clinical activities. You will also mentor team members, promote best practices, and contribute to the continuous improvement of quality assurance processes.
What you bring
You, as the ideal Sr. QA/GCP specialist/manager will recognise yourself in the following:
- Bachelor or Master degree in Pharmacy, Biotechnology, or a related field
- 5+ years of experience in GCP quality assurance, clinical operations, or regulatory compliance within the biotechnology, pharmaceutical, or medical device industry
- Strong analytical and problem-solving skills to assess compliance risks and implement improvements.
What's in it for you
What we offer:
- Competitive salary
- Performance bonus
- 30 holidays
- Pension scheme
- Meaningful Impact: Contribute to innovative healthcare solutions that make a real difference
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