Quality Assurance Director (Clinical)
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 Noord-Holland Netherlands.
- Be back-up for the department head
- Advise and consult other departments on cGMP matters
- Steer the CMOs on a daily basis and audit suppliers on a regular basis.
- You have at least 8 years of experience in a similar role
- You will have to bring result-orientedness, integrity, tenacity
- Having communication skills and networking skills are important to be a success
- You are a team player who builds relationships to make sure they have excellent cooperation with the business partners
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
The Company
This company is committed to making their treatments against life-threatening diseases as effective as possible. It is their goal to increase life expectancy.Role Description
You are a peoples manager with dedication to bring the most out of the team? Do you want to work at an international company where your input really counts? You love traveling to your clients to build up a long term relationships? Then this is the job you!Responsibilities
You will be responsible for managing and resolving the QA related non-conformances at CMOs and suppliers. You will provide support to their external parties and ensure completeness and correctness of documentation. Next to that you will be responsible for the following:- Be back-up for the department head
- Advise and consult other departments on cGMP matters
- Steer the CMOs on a daily basis and audit suppliers on a regular basis.
Requirements
- MSc degree biotechnology or pharmaceutical industry- You have at least 8 years of experience in a similar role
- You will have to bring result-orientedness, integrity, tenacity
- Having communication skills and networking skills are important to be a success
- You are a team player who builds relationships to make sure they have excellent cooperation with the business partners
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
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