CQV Engineer

CQV Engineer
Voir toutes les offres

CQV Engineer

Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI
1/14/2026
POSTULER

Vos responsabilités

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
  • Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
  • Participate in design reviews (URS, FDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
  • Manage execution of commissioning and qualification activities in alignment 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 FAT and SAT with suppliers and engineering teams.
  • Troubleshoot and resolve technical issues encountered during CQV execution.
  • Ensure all CQV deliverables meet internal Quality and Validation standards, and align with site Validation Master Plan (VMP).
  • Support 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 the promotion of Antaes services on top of assistance provided to clients.

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
  • Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
  • Participate in design reviews (URS, FDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
  • Manage execution of commissioning and qualification activities in alignment 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 FAT and SAT with suppliers and engineering teams.
  • Troubleshoot and resolve technical issues encountered during CQV execution.
  • Ensure all CQV deliverables meet internal Quality and Validation standards, and align with site Validation Master Plan (VMP).
  • Support 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 the promotion of Antaes services on top of assistance provided to clients.

Votre profil

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 CQV 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).
  • Candidate must be highly motivated, be 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 liase with English speaking counterparts.

À propos d'Antaes

Créée en 2007, Antaes est une société suisse de conseil en management et technologie classée dans le top 15 des sociétés de conseil en Suisse. Nous comptons plus de 300 ingénieurs expérimentés qui partagent notre passion.

 

Présents en Suisse, à Singapour, à Hong-Kong et en France, nous accompagnons nos clients suisses, et internationaux en intervenant dans les domaines suivants :

  • Conseil en organisation et transformation
  • Ingénierie Industrielle
  • Management des systèmes d'Information

 

En rejoignant nos équipes vous découvrirez :

  • Une équipe dynamique dans un esprit start-up
  • Un accompagnement humain et un suivi de l’évolution de votre carrière
  • Des challenges pour contribuer au développement de votre réseau
  • Des événements : team building, meet-up, workshop, Winter Event …
  • Une entreprise certifiée @HappyAtWork et ayant une politique RSE engagée (médaille d’or Ecovadis2023)

POSTULER
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En tant que Ingénieur Software .NET Core F/H, vos missions seront :

 

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Key Responsibilities

  • Manage the full-cycle recruitment process including job posting, sourcing, screening, interviewing, and offer management.
  • Manage salary negotiation, prospection, sales activities, inbounds, outbounds, and client relationships.
  • Proactively source passive candidates through LinkedIn Recruiter, job boards, industry networks, and talent pipelines.
  • Build and maintain a strong pipeline of qualified candidates for current and future hiring needs.
  • Leverage niche platforms and life sciences talent communities to identify specialized candidates.
  • Collaborate with hiring managers to define role requirements, ideal candidate profiles, and hiring timelines.
  • Provide regular updates, market insights, and data-driven recommendations to stakeholders.
  • Act as a trusted advisor on talent availability, compensation benchmarks, and recruitment best practices.
  • Deliver a best-in-class candidate experience throughout the entire recruitment journey.
  • Maintain timely and transparent communication with all candidates.
  • Represent the company brand authentically and compellingly to prospective hires.
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  • Identify trends and suggest improvements to enhance recruitment efficiency.
  • Contribute to social media content and outreach that highlights company culture and opportunities.
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CDI
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Key Responsibilities

  • Risk Assessment and Data Protection: Conduct risk assessments and workshops to understand data protection scenarios and challenges within the organization.
  • CSRIT & DLP Tool Implementation: Work with DLP tools to identify and prevent risky data movements and ensure DLP controls are effective in protecting sensitive data assets.
  • Regulatory Compliance: Ensure compliance with data privacy and protection regulations, both business-related and regulatory.
  • Documentation and Requirements: Document business requirements, develop data protection scenarios, and create use cases for DLP tools.
  • Stakeholder Collaboration: Engage with business and IT stakeholders to define data security needs and implement controls.
  • Policy and Process Improvement: Partner with other teams to optimize existing DLP controls, identify new risks, and develop a DLP maturity plan.
  • Testing and Sign-off: Perform functional and technical testing of DLP policies and processes to ensure robust solutions are delivered.
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Quality Assurance Associate

Asia - Singapore
CDI
Ingénierie Industrielle et Life-Science

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Review and verify executed component batch records for accuracy and compliance with GMP/GDP requirements.
  • Perform timely release of raw materials, buffers, and media in SAP in accordance with approved specifications and procedures.
  • Support Electronic Batch Record (EBR) review activities for production operations.
  • Participate in Quality on the Floor (QOTF), GEMBA walks, and provide real-time guidance to operations personnel on documentation practices and GMP compliance.
  • Assist in identifying and escalating documentation or process deviations during record review or shopfloor interactions.
  • Collaborate cross-functionally with Production, QC, and Material Management teams to resolve discrepancies or issues related to material release and batch documentation.
  • Support QA team in continuous improvement initiatives and data gathering for metrics and trend analysis.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients
Voir l'offre

Maintenance Technician (Process Equipment)

Asia - Singapore
CDI
Ingénierie Industrielle et Life-Science

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Perform routine preventive, corrective, and predictive maintenance on manufacturing and utility equipment (e.g. bioreactors, chromatography skids, ultrafiltration systems, mixers, autoclaves, CIP/SIP systems).
  • Troubleshoot mechanical/electrical issues to minimize equipment downtime and support uninterrupted production.
  • Assist in equipment installation, commissioning, and qualification (IQ/OQ/PQ) in compliance with regulatory expectations.
  • Create and update Bill of Materials (BOMs), spare parts lists, and maintenance documentation in CMMS/ERP systems.
  • Execute maintenance activities according to SOPs, GMP, safety, and EHS standards.
  • Support root cause investigation and implement corrective/preventive actions (CAPA) for equipment-related deviations.
  • Collaborate with cross-functional teams including Manufacturing, Engineering, Validation, and Quality.
  • Participate in continuous improvement initiatives to enhance equipment reliability and lifecycle management.
  • Participate in design reviews, HAZOPs, FATs/SATs as needed for utility and equipment systems.
  • Contribute to the promotion of Antaes services on top of assistance provided to clients
Voir l'offre
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CQV Engineer

Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI

Vos responsabilités

This is some text inside of a div block.

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
  • Support end-to-end CQV lifecycle for process, utility, and support systems — e.g. bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
  • Participate in design reviews (URS, FDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
  • Manage execution of commissioning and qualification activities in alignment 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 FAT and SAT with suppliers and engineering teams.
  • Troubleshoot and resolve technical issues encountered during CQV execution.
  • Ensure all CQV deliverables meet internal Quality and Validation standards, and align with site Validation Master Plan (VMP).
  • Support 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 the promotion of Antaes services on top of assistance provided to clients.

Votre profil

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 CQV 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).
  • Candidate must be highly motivated, be 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 liase 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.

À propos d'Antaes

Créée en 2007, Antaes est une société suisse de conseil en management et technologie classée dans le top 15 des sociétés de conseil en Suisse. Nous comptons plus de 300 ingénieurs expérimentés qui partagent notre passion.

 

Présents en Suisse, à Singapour, à Hong-Kong et en France, nous accompagnons nos clients suisses, et internationaux en intervenant dans les domaines suivants :

  • Conseil en organisation et transformation
  • Ingénierie Industrielle
  • Management des systèmes d'Information

 

En rejoignant nos équipes vous découvrirez :

  • Une équipe dynamique dans un esprit start-up
  • Un accompagnement humain et un suivi de l’évolution de votre carrière
  • Des challenges pour contribuer au développement de votre réseau
  • Des événements : team building, meet-up, workshop, Winter Event …
  • Une entreprise certifiée @HappyAtWork et ayant une politique RSE engagée (médaille d’or Ecovadis2023)