Biotech process validation engineer (F/M)

Biotech process validation engineer (F/M)
See all offers

Biotech process validation engineer (F/M)

Switzerland - Vaud
Industrial Engineering and Life-Science
Permanent
2/9/2024
APPLY

About the role

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.

 

Your profile

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.

About 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!

APPLY
Our other offers

Project Director - Major CAPEX (Aseptic Filling Line)

Switzerland - Neuchâtel
Permanent
Industrial Engineering and Life-Science

Location: Neuchâtel

Start date: Asap

Workload: 100%, on site

 

 

To join our Life Sciences team in Neuchâtel, we are looking for a Project Director - Major CAPEX (Aseptic Filling Line).

 

Lead and coordinate a large-scale capital investment project for a new aseptic filling line. Oversee planning, budget, and milestones, ensuring smooth transition from project phase to operations. Act as the project management expert guiding technical teams and senior leaders.

 

 

The project:

  • Manage project completion, including Engineering Runs (ER) and Process & Performance Qualification (PPQ).
  • Coordinate communication and reporting with site leadership, global teams, and external partners.
  • Track and control project schedules, budgets, resources, and risks.
  • Ensure compliance with policies and good project management practices.
  • Facilitate meetings, support change management, and manage handover to operations.
  • Develop contingency and risk mitigation plans.
See the offer

Project Manager, Methods - Investment Maintenance

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

Location: Geneva, Switzerland

Start date: January 2026

Staffing: 100%, on site

 

 

As part of the development of our industrial activities, we are looking for a Methods Project Manager to support maintenance in the implementation of investment projects.

 

Your role will be to represent maintenance on projects, prepare for the integration of new equipment, and guarantee its maintainability throughout its life cycle.

 

 

Mission:

  • Participate in equipment acquisition projects and monitor their progress.
  • Managing feedback and gathering internal requirements.
  • Coordinate the teams and partners involved.
  • Ensure compliance with technical specifications and schedules.
  • Develop and monitor project performance indicators.
  • Prepare maintenance of new equipment (spare parts, documentation, maintenance plans, training).
  • Carry out maintenance and logistics reviews during and at the end of the project.
See the offer

Project Manager - Hospitals - part-time

Switzerland - Geneva
Permanent
Consulting and Business Management

Location: Geneva, Switzerland

Start date: November 2025

Job occupancy: 60% for 1 year

 

 

We are looking for a part-time Project Manager / PMO consultant to manage a project portfolio in a medical division of our hospital client .

 

 

Mission:

1. Management of the department's project portfolio

  • Preparation and updating of monitoring and reporting dashboards.
  • Examination of project announcements and preparation of the elements required for the departmental committee's decision.
  • Use of One2Team PPM software for project tracking and coordination.
  • Development of a departmental roadmap in line with the client's corporate strategy.

 

2. Project management

  • Manage two projects, including planning, risk management, stakeholder coordination and documentation.
  • Participation and reporting to steering committees.
  • Projects concerned: building renovation and refurbishment.

 

3. Methodological support for departmental and service projects

  • Provide methodological support for priority projects, including: system implementation, development of a new concept and relocation of a unit, extension and securing of a unit, renovation of several units.
See the offer

Continuous Improvement Project Manager - Industrial F/H

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting a Continuous Improvement Project Manager - Industrial F/H on a permanent contract to join our industrial expertise division as part of a large-scale, long-term project to expand our partner's activities.

 

As a Continuous Improvement Project Manager - Industrial F/H, your missions will be :

 

  • Deploy the continuous improvement process across all sectors and ensure overall coordination of the approach.
  • Define the roles and responsibilities of those involved at each stage of the process.
  • Design and run an effective session routine, in line with the objectives of the approach.
  • Set up a coaching system to ensure that the process runs smoothly and is sustainable.
  • Contribute to the implementation and evolution of audits, while defining relevant performance indicators.
  • Structure and formalize the approach through regular reporting and presentations to management.
  • Develop the skills of stakeholders (operations, industrialization, support functions) and support change management.
See the offer

Watchmaking Product Industrialization Methods Engineer F/H

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting a Watchmaking Product Industrialization Methods Engineer F/H on a permanent contract to join our Industrial Expertise division as part of a large-scale, long-term project to expand the activities of our partner in Geneva.

 

As a Watchmaking Product Industrialization Methods Engineer F/H, your responsibilities will include :

 

  • Take charge of technical problems in several production sectors.
  • Analyze and frame requests, assess their impact and coordinate the implementation of changes with business teams.
  • Manage the deployment of changes in production, monitoring the schedule and associated deliverables.
  • Design and deploy a centralized tracking dashboard for all requests.
  • Organize regular reporting points with Production teams and the business lines concerned.
  • Lead continuous improvement projects (CIP) upstream of the change flow.
  • Monitor and control references to be launched in production whose industrial files are incomplete.
See the offer
APPLICATION FORM
* required fields
By submitting this form, you acknowledge that you have read our website's privacy policy, which includes your rights regarding your personal data.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Biotech process validation engineer (F/M)

Switzerland - Vaud
Industrial Engineering and Life-Science
Permanent

About the role

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.

 

Your profile

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.

About 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!