Quality Assurance Officer / Utrecht / GMP & GDP
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 Utrecht Netherlands.
- Handling the complaint according the internal work instructions
- Documenting various processes
- Database management
- At least 2 years experience within the QA
- Experience within the GMP or GDP is required, both is a plus
- Experience in- and passion for administrative work
- You are accurate and service oriented
- You speak english and dutch fluently
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.
The Company
This pharmaceutical company is focused on the prevention, relief and healing of various diseases to improve the quality of life by innovating products and solutions. They aim to achieve this goal by using biochemical processes in living organisms. Within this company the focus is on delivering a good quality with personal attention for the patients.Role Description
In addition to the current Regulatory Affairs quality department they are looking for a QA officer with experience in the GMP and GDP environment who is capable of ensuring the compliance of current regulations with the QMS. They are looking for an officer who specializes in administrative work and has a lot of knowledge of Quality Management SystemsResponsibilities
- Keeping the QMS up-to-date- Handling the complaint according the internal work instructions
- Documenting various processes
- Database management
Requirements
- A pharmaceutically oriented degree- At least 2 years experience within the QA
- Experience within the GMP or GDP is required, both is a plus
- Experience in- and passion for administrative work
- You are accurate and service oriented
- You speak english and dutch fluently
Other information
Within this company we will invest in you and your career by offering you a competitive salary, but also an inspiring work environment with the possibilities to grow.Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ria Bos.
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