Validation Engineer GMP
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 Biotechnology and Pharmaceutical organization, based in Noord-Brabant Netherlands.
Pharmaceutical company that offers the opportunity to develop and grow within the company. There is a large portfolio of Pharmaceutical and biotech products.
ROLE DESCRIPTION
The Validation Engineer will be responsible for developing a validation impact assessment for change requests. It is expected that the Validation Engineer faces highly complex technical issues.
Information
- Type of contract: temporary via Freelance (ZZP) or Payroll
- Location: Breda, The Netherlands
- Duration: 6 months (minimum)
- FTEs: full-time
RESPONSIBILITIES
- Develop a validation impact assessment for change requests
- Provide solutions to a variety of highly complex technical validation problems
- Independently evaluate, select and apply standard validation engineering techniques, policies, procedures and criteria
- Develop requirements and recommendation for system modifications
- Participate in several projects and occasionally set deadlines and budget constraints
Main projects content
- Pharma Controlled Temperature mapping
- Pharma secondary packaging, including MES and Serialization
REQUIREMENTS
- Strong knowledge and working experience applying Validation principles, concepts, theories and standards
- Previous experience in a pharmaceutical GMP environment
- Work under minimal supervision
- Advanced English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
