Biotech process validation engineer (F/M)

Biotech process validation engineer (F/M)
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Biotech process validation engineer (F/M)

Suisse - Vaud
Ingénierie Industrielle et Life-Science
CDI
2/9/2024
POSTULER

Vos responsabilités

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.

 

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.

 

Votre profil

This is some text inside of a div block.
  • 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.

À propos d'Antaes

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.

  • Organisation and transformation consulting
  • Industrial Engineering
  • Information Systems Management

 

By joining our team you will discover :

  • A dynamic team in a start-up spirit
  • A human accompaniment and a follow-up of your career development
  • Challenges to contribute to the development of your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • A company certified @HappyAtWork and with a committed CSR policy (Ecovadis2023 gold medal)

You too can be part of the Antaes adventure !

POSTULER
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  • Proposer des concepts en tenant compte des objectifs
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Biotech process validation engineer (F/M)

Suisse - Vaud
Ingénierie Industrielle et Life-Science
CDI

Vos responsabilités

This is some text inside of a div block.

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.

 

Votre profil

This is some text inside of a div block.
  • 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.

Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis.

À propos d'Antaes

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.

  • Organisation and transformation consulting
  • Industrial Engineering
  • Information Systems Management

 

By joining our team you will discover :

  • A dynamic team in a start-up spirit
  • A human accompaniment and a follow-up of your career development
  • Challenges to contribute to the development of your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • A company certified @HappyAtWork and with a committed CSR policy (Ecovadis2023 gold medal)

You too can be part of the Antaes adventure !