QA Specialist / Pharma / Area of Amsterdam / 45-55K
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Noord-Holland Netherlands.
- Supervising Contract Manufacturing projects
- Performing internal audits
- Project management within the Pharmaceutical Affairs department
- Handling deviations, CAPAs and change controls
- At least 5 years of experience in the Pharmaceutical Industry
- Familiar with EU GMP and GDP regulations
- Experience with Batch review
- Preferably you have experience with coaching and performing audits
- Good command of Dutch and English language
Experience in the following areas is an advantage:
- Knowledge of quality systems (GMP / GDP)
- Experience with qualification and validation
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Turlough White.
The Company
With a wide range of generic medicines on the market such as cardiovascular, dermatological, antibiotics, antihistamines, antidepressants and a range of inhalations products. This company has all disciplines in-house for product development. With a dedicated professional team, the highest standards are pursued in the areas of Registration, Quality, Pharmacological and Supply Chain.Role Description
As QA Specialist you will support and report to the QA Manager by performing independent activities in the field of Quality Assurance. Perform internal audits, Batch reviews, change and CAPA, update SMF and SOP's. Additionally supervising Contract Manufacturing and Analytical Method Transfer projectsResponsibilities
- Review of batch documentation for QP certification- Supervising Contract Manufacturing projects
- Performing internal audits
- Project management within the Pharmaceutical Affairs department
- Handling deviations, CAPAs and change controls
Requirements
- At least HBO level- At least 5 years of experience in the Pharmaceutical Industry
- Familiar with EU GMP and GDP regulations
- Experience with Batch review
- Preferably you have experience with coaching and performing audits
- Good command of Dutch and English language
Experience in the following areas is an advantage:
- Knowledge of quality systems (GMP / GDP)
- Experience with qualification and validation
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Turlough White.
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