QA Specialist with leadership ambition
Location: BelgiumSIRE® 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 Limbourg Belgium.
- Managing permits and ensure compliancy with the regulations
- Coach and supervise a team of 10 RPs (distributed in Europe) globally
- Reviewing contracts regarding the quality requirements
- Manage and analyze the internal and external quality (KPIs)
- Contact person and networking with authorities
- Support quality-related projects
- You will travel around 20% of the time.
- At least 5 years of working experience in life science industry
- Good knowledge of relevant quality standards (GDP, GMP, ISO9001 ...)
- Thorough knowledge of Dutch and English, both spoken and written
- Excellent coaching skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
The Company
Our client is a big international company who is also operating in the QA Supply Chain / Logistics. They offer an interesting and ambitious job opportunity with a leadership aspect. A challenging working environment with numerous growth opportunities.Role Description
You are responsible for ensuring the QMS and compliancy regarding all regulations. You will be trained as RP (Responsible Person) for the company. This includes the development and optimization of an integrated quality management system in terms of environment, safety, quality and food safety. In this role you will lead a team od other responsible person globally (10 FT). You will travel around 20% of the time.Responsibilities
- Responsible for changes within the (inter) national legislation regarding pharmaceutical, food and chemical products and implement/communicate this with our clients- Managing permits and ensure compliancy with the regulations
- Coach and supervise a team of 10 RPs (distributed in Europe) globally
- Reviewing contracts regarding the quality requirements
- Manage and analyze the internal and external quality (KPIs)
- Contact person and networking with authorities
- Support quality-related projects
- You will travel around 20% of the time.
Requirements
- MSc. (Industrial) Pharmacy, pharmaceutical sciences, medicine, veterinary medicine, chemistry, biology or master in biomedical sciences- At least 5 years of working experience in life science industry
- Good knowledge of relevant quality standards (GDP, GMP, ISO9001 ...)
- Thorough knowledge of Dutch and English, both spoken and written
- Excellent coaching skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
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