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SIRE Life Sciences
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Fulltime
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Junior/Medior/Senior
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Engels (taal)
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Vacature in het kort
As a Sr. Associate QA, you'll ensure compliance within a regulatory environment, develop solutions to technical problems, and manage product quality complaints and safety investigations. You'll perform assessments, review batch records, and participate in site regulatory inspections. This role offers a unique opportunity to contribute to groundbreaking medical advancements. Take the next step and explore why this role is a great fit for you.Volledige vacaturetekst
Sr. Associate QA
The Company
Our client is an innovative leader on the field of pharmaceutical biotechnology. Over the past 40 years, they have been pioneers in developing revolutionary medicine to help ill people around the world.
The Role
As an Associate Quality Assurance, you will be responsible for ensure compliance within regulatory environment, develops solutions to technical problems, as well initiate and own product quality complaints, safety quality investigations and product security investigations.
Responsibilities
– Perform assessments in support of complaint investigations, batch record review, reserve sample inspection, Return sample inspection.
– Prepare, review and approve procedures or work instructions in compliance with corporate, site and regulatory requirements.
– Initiate and own QA Non-Conformances/CAPAs as needed.
– Participate in site regulatory inspections of complaint handling process and in audits.
Requirements
– Bachelor’s degree or Master degree in related field.
– Typically, 3 or more years of related professional experience
– Fluent in English language.
– Experience in Quality Assurance, including handling product complaints investigations.
– Experience in pharmaceutical industry.
Other information
Are you ready to the next step in your career? Feel free to contact me.
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