QA Manager
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 Zuid-Holland Netherlands.
- You optimize the quality management system, processes and procedures with the objective of optimizing the functioning of all quality processes.
- You support both internal and external quality audits and you implement the necessary actions resulting from these audits.
- You coordinate and investigate quality issues such as non-conformities, complaints about product quality, etc. You prepare action plans and adjust where necessary.
- You have a thorough knowledge of QA systems and GxP requirements, including regulations and standards that affect medical devices, nutritional supplements and other pharmaceutical products.
- You are analytical and think problem solving with a focus on continuous improvement.
- You have strong communication skills in Dutch/English and preferably French
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
The Company
For a very interesting pharmaceutical company I am looking for a qualified QA Manager.Role Description
As a QA Manager and Responsible Person you are responsible for GDP (Good Distribution Practices) requirements for the different countries in which the company carries out distribution activities for medicines.Responsibilities
- You are responsible for the follow-up and implementation of new legislation and quality standards.- You optimize the quality management system, processes and procedures with the objective of optimizing the functioning of all quality processes.
- You support both internal and external quality audits and you implement the necessary actions resulting from these audits.
- You coordinate and investigate quality issues such as non-conformities, complaints about product quality, etc. You prepare action plans and adjust where necessary.
Requirements
- Masters in Pharmaceutical Sciences, Medicine, Chemistry or similar.- You have a thorough knowledge of QA systems and GxP requirements, including regulations and standards that affect medical devices, nutritional supplements and other pharmaceutical products.
- You are analytical and think problem solving with a focus on continuous improvement.
- You have strong communication skills in Dutch/English and preferably French
Other information
Are you interested or do you want to know more about this position? Do not hesitate to call me, reply to this message or send an e-mail to j.zanting@sire-search.com !Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
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