SIRE Life Sciences®

Project Manager

Location: Netherlands
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 looking for a project manager who can represent and manage the delivery of their site and NPI (New Product Introduction) 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 the 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.

Role Description

They will work directly with SMEs, vendors and customers to ensure regulatory (e.g. validation), business, functional and application specific requirements are met.
The role will also require the generation of proposals for the 2019 program.

Responsibilities

- Execute projects to Project Execution Plan (PEP) and meet all GMP requirements.
- Ensure the highest levels of project safety.
- Perform continual project risk analysis.
- Identify project critical paths and prioritize accordingly.
- Discover and understand end-user/process requirements; translate these into user requirements specifications.
- Manage the compilation of all project documentation.
- 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 Dutch standards.
- Set up and manage communication channels – Weekly report out/Project Team Meetings.
- Managing Key business stakeholders expectations/interactions (Planning, Manufacturing, Warehouse & Distribution, Customer Service and Quality).

Requirements

- Project management qualification or 5+ years PM experience
- MS Project
- Cost/budget control
- Change management
- Excellent communication skills

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
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SIRE Life Sciences®

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