CSV engineer
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Zuid-Holland Netherlands.
he client is a leading pharmaceutical in Europe with presence in all European markets. They have specialists working on its commercial, development and manufacturing operations and manages all aspects of product development, production, marketing, sale and supply.
ROLE DESCRIPTION
Are you a passionate Process Engineer or are you a Computerized quality system expert with a few years of relevant work experience? Do you want a position where you can act as first point of contact? Do you have interest in Lean/six sigma? Then this is the perfect job for you!
RESPONSIBILITIES
You will be responsible to acts as a Center of Expertise for GMP Computerized Quality Systems and as single point of contact. Also you will maintains and improves GMP Computerized Quality Systems, ensuring that the state-of-the-art technology is up tot date. next to that you will be responsible for the following:
- Is responsible for all project aspects of Computerized Quality Systems improvement initiatives and application updates
- Project lead for local Quality Systems initiatives
- Cooperates with the global Computerized Quality Systems team to develop and maintain the standards for regulatory compliance, e.g. on Data Integrity.
- Provides support to the end users, resolves issues, and performs troubleshooting.
REQUIREMENTS
- Pharmaceutical or related industry work experience with minimum 2-3 years relevant to this role
- Experience in a multinational work environment/company is a pre.
- Project management skills and interpersonal skills, engaged in contact with personnel at all levels within the organization.
- Written and oral communication skills in English. Dutch is preferable.
- Self-starter, planning skills, and ability to prioritize multiple commitments.
- Analytical thinking and (technical) problem solving. Lean/Six Sigma experience is desirable.
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.
