Project Manager API manufacturing
Location: BelgiumSIRE® 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 Brussels Hoofdstedelijk Gewest Belgium.
- 3-5 years of experience in a similar role
- GMP knowledge
- Peptide knowledge is considered a plus
- Fluent in French
- Strong organizer with natural sense for overview
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
The Company
Our client is an international contract manufacturer of active pharmaceutical ingredients, servicing both pharmaceutical and biotech companies.Role Description
As the project manager you will be working at the manufacturing subsidiary where you will lead from 5 up to 10 projects at the same time. This position reports directly to the Head of project management. You will also engage with clients to discuss and probe their needs in order to set up a project for success.Responsibilities
You are responsible for project set-up; milestone indications; making sure that projects run smoothly on time, within budget. You are the center figure between manufacturing, clients and the vendors while maintaining relationships with all stakeholders. You prioritize your own work and perform all risk assessments and gap analysis.Requirements
- A degree in engineering, biotech or pharmaceutical sciences- 3-5 years of experience in a similar role
- GMP knowledge
- Peptide knowledge is considered a plus
- Fluent in French
- Strong organizer with natural sense for overview
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
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