Project Engineer

Project Engineer
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Project Engineer

Asia - Singapore
Industrial Engineering and Life-Science
Permanent
January 27, 2026
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About the role

Job Description

  • Contribute to Life Science projects for Antaes Asiaclients.
  • Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. 
  • End-to-end C&Q lifecycle support for process, utility, and support systems—e.g., bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities. 
  • Manage the execution of commissioning and qualification activities in line with project schedules, safety standards, and GMP compliance. 
  • Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems. 
  • Review vendor documentation and coordinate SAT with suppliers and engineering teams. 
  • Troubleshoot and resolve technical issues encountered during C&Q execution. 
  • Ensure all C&Q deliverables meet internal Quality and Validation standards, and align with the site Validation Master Plan (VMP).
  • Support the handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
  • Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
  • Contribute to promoting Antaes services in addition to providing assistance to clients. 

Job Description

  • Contribute to Life Science projects for Antaes Asiaclients.
  • Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. 
  • End-to-end C&Q lifecycle support for process, utility, and support systems—e.g., bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities. 
  • Manage the execution of commissioning and qualification activities in line with project schedules, safety standards, and GMP compliance. 
  • Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems. 
  • Review vendor documentation and coordinate SAT with suppliers and engineering teams. 
  • Troubleshoot and resolve technical issues encountered during C&Q execution. 
  • Ensure all C&Q deliverables meet internal Quality and Validation standards, and align with the site Validation Master Plan (VMP).
  • Support the handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
  • Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
  • Contribute to promoting Antaes services in addition to providing assistance to clients. 

Your profile

This is some text inside of a div block.

Job Requirements: 

  • Bachelor's Degree in Chemical, Mechanical, Biomedical, or related Engineering field.
  • 3–7 years of quality, safety, and environment (QSE) experience in the pharmaceutical industry  
  • Strong understanding of GMP, GEP, ISPE Baseline Guides, ASTM E2500, and FDA/EMA validation expectations. 
  • Experience in process equipment qualification (bioreactors, chromatography, UF/DF, CIP/SIP), clean utilities, and automation integration. 
  • Familiar with risk-based CQV approach and change control processes. 
  • Proficiency with documentation management systems (e.g., Veeva) 
  • Candidates must be highly motivated, able to work independently as well as in a team, and have good organizational and oral and written communication skills. 
  • Excellent communication skills, both written and verbal, in English - to coordinate and liaise with English-speaking counterparts.

About Antaes

Founded in 2007, Antaes is a Swiss management and technology consulting company ranked among the top 15 consulting firms in Switzerland. We employ over 300 experienced consultants who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international customers at clients in the following areas:

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

 

By joining our teams you will discover :

  • A dynamic team in a start-up spirit
  • Human support and career development monitoring
  • Challenges to help develop your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • An @HappyAtWork certified company with a committed CSR policy (Ecovadis2023 Gold Medal)

APPLY
Our other offers

Project Engineer

Asia - Singapore
Permanent
Industrial Engineering and Life-Science

Job Description

  • Contribute to Life Science projects for Antaes Asiaclients.
  • Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. 
  • End-to-end C&Q lifecycle support for process, utility, and support systems—e.g., bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities. 
  • Manage the execution of commissioning and qualification activities in line with project schedules, safety standards, and GMP compliance. 
  • Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems. 
  • Review vendor documentation and coordinate SAT with suppliers and engineering teams. 
  • Troubleshoot and resolve technical issues encountered during C&Q execution. 
  • Ensure all C&Q deliverables meet internal Quality and Validation standards, and align with the site Validation Master Plan (VMP).
  • Support the handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
  • Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
  • Contribute to promoting Antaes services in addition to providing assistance to clients. 
See the offer

Automation Engineer

Asia - Singapore
Permanent
Industrial Engineering and Life-Science

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients.
  • Lead the review, closure, and follow-up of I/O and Loop Check qualification protocols.
  • Identify and track discrepancies found during loop checks (e.g., wiring errors, signal scaling issues, or hardware faults) and drive them to closure with the electrical and instrumentation (E&I) teams.
  • Ensure that every physical instrument correctly communicates with the DeltaV system according to the P&IDs and Functional Specifications.
  • Perform qualification deliverables for DeltaV coding, including Phase Logic, Module testing, and Graphics verification.
  • Perform on-site software testing and dry runs during the Water Batching/Startup phases to ensure code aligns with process requirements.
  • Manage software versions and formal Change Controls during the transition from the "build" phase to the "validated" state.
  • Create and manage pre-execution documents (e.g., test scripts, user requirement specifications, functional design specifications).
  • Compile post-execution summary reports, ensuring all "As-Built" documentation is accurate and compliant with Data Integrity standards.
  • Maintain the automation validation master file to be ready for regulatory inspections (FDA/EMA).
  • Contribute to the promotion of Antaes services on top of assistance provided to clients.
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Industrial Engineering and Life-Science

We are recruiting an Industrial Robotics Engineer - Live Tracking (M/F) on a permanent contract to join our expertise center as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As an Industrial Robotics Engineer - Live Tracking, your responsibilities will include:

 

  • Develop and optimize embedded code (C/C++, Python, ROS/ROS2, LabVIEW).
  • Program trajectories, direct/reverse kinematics, safety and sensor management.
  • Configure and program industrial robots (Fanuc, Kuka, UR, ABB...).
  • Integrate the robot into its industrial or R&D environment.
  • Carry out tests, validations, performance measurements and fault analysis.
  • Interface with PLCs, industrial equipment and systems.
  • Define preventive and corrective maintenance procedures.
  • Diagnose mechanical/electrical/software faults.
  • Train users (operators, technicians, production teams).
See the offer

Industrial Metrologist - Dimensional Control M/F

Switzerland - Vaud
Permanent
Industrial Engineering and Life-Science

We are recruiting an Industrial Metrologist - Dimensional Control (M/F) 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 an Industrial Metrologist - Dimensional Control, your responsibilities will include:

 

  • Perform physical measurements using three-dimensional inspection equipment such as coordinate measuring machines (CMMs), laser trackers, and Faro polyarticulated measuring arms.
  • Ensure the programming, validation, and optimization of 3D measurement programs, ensuring their performance and compliance with metrological requirements.
  • As a leader in three-dimensional metrology, you also play a training role for internal teams. In this capacity, you assist technicians in learning how to use 3D equipment and applying best measurement practices.
  • Develop and implement metrology procedures, instruction sheets, and related monitoring documents.
  • Write inspection reports by analyzing, interpreting, and utilizing measurement results and statistical data.
  • You will occasionally visit suppliers in Europe (approximately 10% of the time), where you will carry out checks during the manufacturing process, analyze non-conformities, and write the associated reports.
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Watchmaking Product Industrialization Project Manager F/H

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We are recruiting a Watchmaking Product Industrialization Project Manager 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 Project Manager, your responsibilities will include :

 

 

  • Plan and lead technical convergence reviews, including process plans, controls and capabilities.
  • Develop and industrialize ranges and bills of materials for new products.
  • Manage activity planning and risk management.
  • Unite the resources involved.
  • Manage and implement product and process evolutions, adapting the governance of series during their life cycle.
  • Capitalize on best practices and contribute to the development of reference systems.
  • Manage the model plan approach in line with industrial tool capacities.
See the offer
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Project Engineer

Asia - Singapore
Industrial Engineering and Life-Science
Permanent

About the role

This is some text inside of a div block.

Job Description

  • Contribute to Life Science projects for Antaes Asiaclients.
  • Develop and execute C&Q documentation including commissioning protocols, SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices. 
  • End-to-end C&Q lifecycle support for process, utility, and support systems—e.g., bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities. 
  • Manage the execution of commissioning and qualification activities in line with project schedules, safety standards, and GMP compliance. 
  • Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems. 
  • Review vendor documentation and coordinate SAT with suppliers and engineering teams. 
  • Troubleshoot and resolve technical issues encountered during C&Q execution. 
  • Ensure all C&Q deliverables meet internal Quality and Validation standards, and align with the site Validation Master Plan (VMP).
  • Support the handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
  • Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
  • Contribute to promoting Antaes services in addition to providing assistance to clients. 

Your profile

This is some text inside of a div block.

Job Requirements: 

  • Bachelor's Degree in Chemical, Mechanical, Biomedical, or related Engineering field.
  • 3–7 years of quality, safety, and environment (QSE) experience in the pharmaceutical industry  
  • Strong understanding of GMP, GEP, ISPE Baseline Guides, ASTM E2500, and FDA/EMA validation expectations. 
  • Experience in process equipment qualification (bioreactors, chromatography, UF/DF, CIP/SIP), clean utilities, and automation integration. 
  • Familiar with risk-based CQV approach and change control processes. 
  • Proficiency with documentation management systems (e.g., Veeva) 
  • Candidates must be highly motivated, able to work independently as well as in a team, and have good organizational and oral and written communication skills. 
  • Excellent communication skills, both written and verbal, in English - to coordinate and liaise with English-speaking counterparts.
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 among the top 15 consulting firms in Switzerland. We employ over 300 experienced consultants who share our passion.

 

With offices in Switzerland, Singapore, Hong Kong and France, we support our Swiss and international customers at clients in the following areas:

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

 

By joining our teams you will discover :

  • A dynamic team in a start-up spirit
  • Human support and career development monitoring
  • Challenges to help develop your network
  • Events: team building, meet-up, workshop, Winter Event ...
  • An @HappyAtWork certified company with a committed CSR policy (Ecovadis2023 Gold Medal)