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.
Job Description
SIRE 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.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control / Production Audit
