GMP Project Engineer

SIRE Life Sciences® - More jobs by this advertiser
SIRE® 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.

The Company

This client is an international pharmaceutical organization, specialized in the packaging and distribution of medicines with a powerful sense of shared purpose toward their mission: to serve patients.

Role Description

Our client is looking for a GMP Project Engineer who can represent and manage the delivery of engineering and maintenance projects. The delivery of these projects will require GMP utility, facility and supporting system changes.

The successful candidate must have the discipline and technical knowledge to work independently and take on responsibilities as demanded by these projects. They must investigate and deploy innovative solutions to improve the efficiency of our current installations. They must ensure procedures are followed and new systems are implemented in compliance with FDA/EMA and other regulatory requirements.

They will work directly with the company's SMEs, vendors and customers to ensure regulatory (e.g. validation), business, functional and application specific requirements are met.


- Execute projects to the company's Project Execution Plan (PEP) and meet all GMP requirements;
- Ensure the highest levels of project safety;
- Identify project critical paths and prioritize accordingly;
- Discover and understand end-user/process requirements; translate these into user requirements specifications;
- Compile all project documentation including URS/FS/HDS/FAT/SAT/TOPs;
- Manage design inputs to ensure robust, testable requirements are established and accurately reflect user and safety needs;
- Manage day to day project activities including permitting/method statement review etc.;
- Develop and document strong rational for testing strategy, acceptance criteria, and results;
- Generate, review, and/or approve protocols, reports ensuring robust documentation for regulatory adherence;
- Monitor installation quality and record inspections – Comply to the company and Dutch standards;
- Set up and manage communication channels – Weekly report out/Project Team Meetings;
- Follows a strict handover process to allow for future system maintenance.


- 5-10 years mechanical/projects background;
- 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 Michelle Tang.

SIRE Life Sciences®

Amsterdam, (Netherlands)

Phone: +31 (0)20 658 9800

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Company Profile

14 August 2019
Location: Netherlands Noord-Brabant Noord-Brabant
Salary: Competitive Salary
Work type:
Life Sciences

This career opportunity is no longer open.
Please search for current vacancies here.

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