Senior QA Specialist
4 weeks ago
About the Role:
As a Senior QA Specialist, you will be responsible for supporting small biotech and pharmaceutical companies in crafting innovative new products. You will also architect and refine Quality Management Systems for emerging pharmaceutical firms. Additionally, you will serve as a QA specialist for the GCP/GMP site in Glostrup and conduct audits on various companies, including suppliers/vendors, with occasional travel.
Your Key Responsibilities:
- Develop and implement Quality Management Systems for pharmaceutical companies.
- Conduct audits and provide recommendations for improvement.
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
- Provide training and support to clients on Quality Management Systems.
Requirements:
- Proven experience in QA work and QMS maintenance within a pharmaceutical setting.
- Fluency in both written and spoken English and Danish.
- Experience in aseptic preparation and the ability to release biological products (a plus).
- Hold qualifications that make you eligible to become QP/QP Delegate.
- Experience with pharmaceutical manufacturing.
Why This Role?
This is an exciting opportunity to join a dynamic team and contribute to the development of innovative pharmaceutical products. As a Senior QA Specialist, you will have the opportunity to work with a variety of clients and projects, and to develop your skills and expertise in Quality Management Systems.
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