Responsible Person (travel of 20%)
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 Luxembourg 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.
- 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 Amber Moet.
The Company
They are a large international company within the Supply Chain / Logistics. The client offers a challenging work environment with numerous growth opportunities.Role Description
As Responsible Person you are responsible for ensuring the QMS. 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 of 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
- Responsible Person (GDP) in accordance with 956§2 of the Royal Decree of 14 December 2006 concerning medicines for human and veterinary use- 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 Amber Moet.
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