QA Specialist/ Pharma / Permanent / Gelderland / The Netherlands / GMP + GDP / Validation & Qual
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 Gelderland Netherlands.
- Contact point for quality issues, both other departments and customers
- Responsible for GMP and GDP regulations
- Give training to staff
- Participate in audits
- Completed study program (HBO / WO) in Life Sciences
- Knowledge of relevant laws and regulations such as GMP, while other standards are a plus (GDP, ISO 9001/13485)
- Team player but also can work independently
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.
The Company
Our client is an international company, based in the Nijmegen, Gelderland. The company is a international company in the Pharmaceutical industry. The company is active in has 220 countries. Our client focuses on accessible care for everyone. They are growing enormously and are working on new construction services that anticipate the future How? By defying all boundaries, to this day.Role Description
As Quality Assurance (QA) Specialist you support the implementation of operational and system changes in such a way that the legal regulations, for the storage and treatment of medicines and medical devices, are followed at the location in Nijmegen.Responsibilities
- Qualification & validation- Contact point for quality issues, both other departments and customers
- Responsible for GMP and GDP regulations
- Give training to staff
- Participate in audits
Requirements
- Extensive experience and affinity in Quality Assurance in a Life Science environment- Completed study program (HBO / WO) in Life Sciences
- Knowledge of relevant laws and regulations such as GMP, while other standards are a plus (GDP, ISO 9001/13485)
- Team player but also can work independently
Other information
Our client is proud that they can provide specialist services in various areas. Life Sciences & Healthcare is a very important branch of sport, because it means that important products can reach the end user in a timely and accurate manner. The location in Nijmegen is fully focused on this sector. Our client is growing enormously and they are working on new services that anticipate the future.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.
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