SIRE Life Sciences®

Validation Manager

Location: Switzerland

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!

THE COMPANY

Our client is a professional Biotechnology and Pharmaceutical organization, based in Basel-Stadt Switzerland.

Our client is focused on established pharmaceuticals.

ROLE DESCRIPTION

Preparation of Process Performance Qualification plans, protocols and reports as well as process risk assessments for complete biopharmaceutical manufacturing processes.

RESPONSIBILITIES

- Preparation of Continued Process Verification documents and carry out trending for selected processes in a timely manner
- Promote and ensures efficient and in-time PPQ in projects according to regulatory and Novartis requirements
- Fulfill the role of validation coordinator for PPQ activities in larger projects
- Availability for PPQ and CPV relevant questions and consulting function for manufacturing
- Support the update of SOPs for production processes and process validation within BP
- Support harmonized validation/documentation approach between Manufacturing plants

REQUIREMENTS

- Education: University studies of Biotechnology, Chemistry, Process Engineering, Microbiology or a similar education
- Languages: fluent in German / English
- Experience: several years of experience in pharmaceutical industry preferably experience with manufacturing processes for biopharmaceuticals, as well as experience with Process Performance Qualification (PPQ)

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.

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SIRE Life Sciences®

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