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Process Development Specialist

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Process Development Specialist

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 Zuid-Holland Netherlands.

The Company

Their mission is to transform individual lives and fundamentally change the way diseases are interpreted, managed and in the end prevented. In over 150 countries the company is bringing innovative science and together with the most creative minds in the industry think differently about diseases. Trying to achieve the best possible results for their health.

Improving the access to medicines, making the best available treatment at an affordable price, starting in this entrepreneurial company will enrich your career!

Role Description

As a Process Development Specialist you will be contributing to process development activities. Involvement in technology transfer to the manufacturing site until manufacturing of process verification and validation batches that are introduced in the global market.

Responsibilities

- Set up, report and timely execution of process development, characterization and validation activities
- Managing different stages of the projects
- Preparing and periodically updating project plans
- Report periodically and escalating when necessary
- Maintain professional relationships with different stakeholders internal and external
- Technical content of the registration dossier, guaranteeing availability of source documentation and raw data
- Lead an participate in specialized committees to ensure continuous improvement on departmental and project level

Requirements

- Bachelor or Master of Science in a relevant field
- Minimal 5 years' of experience in vaccine or large molecule process development
- Strong background in a GMP drug product manufacturing environment
- Experienced with Technology Transfers and outsourcing
- Fluency in English, Dutch is considered a plus
- Strong communication skills, working in an international team

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

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