To join our Life sciences activities, we are looking for a Biotech process validation engineer (F/M), to take part to a long-term project, in partnership with a big pharma company.
Role
Part of the engineering team and in collaboration with quality and production stakeholders, in a context of a biotech manufacturing project (drug products, drug substances), your role is to:
Coordinate process validation activities,
Take part to the design, optimization, improvment, verification and validation of the processes of biotech formulation,
Support Continued Process Verification activities (CPV),
Be involved in the execution of a PPQ (DS DP),
Study the impact of changes on the process, manage the investigations on the process in case of non-conformances,
Ensure the quality (design, validation...) and the good running of the processes.
Engineer/university degree in Biotechnology, Chemistry or Biology or similar,
3 years of experience in biotech process engineering / process design and validation,
Experience in GMP production environment,
Good communication and proactivity,
Team spirit, easiness in a multidisciplinary environment,
Fluent french and profiscient english at least.
Founded in 2007, Antaes is a Swiss management and technology consulting company ranked 7th among consulting companies in French-speaking Switzerland. We have over 300 experienced engineers who share our passion.
With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international clients in the following areas.
By joining our team you will discover :
You too can be part of the Antaes adventure!
To join our Life sciences activities, we are looking for a Biotech process validation engineer (F/M), to take part to a long-term project, in partnership with a big pharma company.
Role
Part of the engineering team and in collaboration with quality and production stakeholders, in a context of a biotech manufacturing project (drug products, drug substances), your role is to:
Coordinate process validation activities,
Take part to the design, optimization, improvment, verification and validation of the processes of biotech formulation,
Support Continued Process Verification activities (CPV),
Be involved in the execution of a PPQ (DS DP),
Study the impact of changes on the process, manage the investigations on the process in case of non-conformances,
Ensure the quality (design, validation...) and the good running of the processes.
Engineer/university degree in Biotechnology, Chemistry or Biology or similar,
3 years of experience in biotech process engineering / process design and validation,
Experience in GMP production environment,
Good communication and proactivity,
Team spirit, easiness in a multidisciplinary environment,
Fluent french and profiscient english at least.
Founded in 2007, Antaes is a Swiss management and technology consulting company ranked 7th among consulting companies in French-speaking Switzerland. We have over 300 experienced engineers who share our passion.
With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international clients in the following areas.
By joining our team you will discover :
You too can be part of the Antaes adventure!