Project Engineer (GMP)
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 organisation, based in Noord-Brabant Netherlands.
engineering and maintenance projects. The delivery of these projects will require GMP utility,
facility and supporting system changes.
• Compile all project documentation including URS/FS/HDS/FAT/SAT/TOPs.
• Ensure the highest levels of project safety.
• Identify project critical paths and prioritize accordingly.
• Generate, review, and/or approve protocols, reports ensuring robust documentation for
regulatory adherence.
• Experience in a Regulated Environment
• MS Project
• Cost/Budget control
• Change Management
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
The Company
One of the largest pharmaceutical companies in the world.Role Description
Our client is looking for a GMP Project Engineer who can represent and manage the delivery ofengineering and maintenance projects. The delivery of these projects will require GMP utility,
facility and supporting system changes.
Responsibilities
• Execute projects to Project Execution Plan (PEP) and meet all GMP requirements.• Compile all project documentation including URS/FS/HDS/FAT/SAT/TOPs.
• Ensure the highest levels of project safety.
• Identify project critical paths and prioritize accordingly.
• Generate, review, and/or approve protocols, reports ensuring robust documentation for
regulatory adherence.
Requirements
• WTB or E• Experience in a Regulated Environment
• MS Project
• Cost/Budget control
• Change Management
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Suleyman Ekiz.
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