Project Coördinator LIMS Implementation
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 and Biotechnology organisation, based in Groningen Netherlands.
- Review and approval van validation documents
- Optimize test method process flows
- Be in charge for IQ/OQ/PQ
- Support of the Quality Department on QA tasks
- Must have minimum 8 years’ experience in a medical device or pharmaceutical GMP
environment. This experience must include working with validation, change control,
test methods (IQ/OQ/PQ)
- Experience with the leading and implementation of LIMS project is highly desirable.
- Familiarity with test method and software validation is a plus.
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
The company is a pharmaceutical multinational which is located in Groningen, Leiden and Breda. For the department of Surgical Vision in Groningen, we are looking for an experience LIMS Implementation Project Coordinator.Role Description
You will be responsible for executing QA Tasks within the Quality Department. You will be the lead for a cross-functional project of LIMS implementation. You have to understand the test-methods, manage the change control process and review/approve validation documents.Responsibilities
- Manage the project of LIMS implemenation- Review and approval van validation documents
- Optimize test method process flows
- Be in charge for IQ/OQ/PQ
- Support of the Quality Department on QA tasks
Requirements
- Master and/or Bachelor Degree in Engineering, Pharmacy, Computer Science- Must have minimum 8 years’ experience in a medical device or pharmaceutical GMP
environment. This experience must include working with validation, change control,
test methods (IQ/OQ/PQ)
- Experience with the leading and implementation of LIMS project is highly desirable.
- Familiarity with test method and software validation is a plus.
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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