Validation engineer - Fluency in English required
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 organisation, based in Netherlands.
Ensure all procedures measure up to required specifications
Evaluate procedures for validation
Work in close collaboration with multidisciplinary departments
Establish validation standards, develop testing protocols, prepare equipment, document test results, prepare risk assessments and ensure handover with final users
You successfully finished a master in (Bio)Medical Engineering or similar
At least 3 years of experience in a Validation job
Experience with systems, cleaning, processes, methods
Ability to comprehend computer systems applications
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
.Role Description
You are going to work with cross-functional departments in order to achieve continuous improvementResponsibilities
Coordinate and execute validation testsEnsure all procedures measure up to required specifications
Evaluate procedures for validation
Work in close collaboration with multidisciplinary departments
Establish validation standards, develop testing protocols, prepare equipment, document test results, prepare risk assessments and ensure handover with final users
Requirements
Familiar with relevant regulations and GxP guidelinesYou successfully finished a master in (Bio)Medical Engineering or similar
At least 3 years of experience in a Validation job
Experience with systems, cleaning, processes, methods
Ability to comprehend computer systems applications
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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