CQV Engineer

CQV Engineer
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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 communicate and work 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
Nos autres offres

Métrologue Industriel - Contrôle Dimensionnel H/F

Suisse - Vaud
CDI
Ingénierie Industrielle et Life-Science

Nous recrutons en CDI un Métrologue Industriel - Contrôle Dimensionnel H/F afin de rejoindre notre pôle d'expertise industrielle, dans le cadre d'un projet de grande envergure et de longue durée d'extension des activités de notre partenaire.

 

En tant que Métrologue Industriel - Contrôle Dimensionnel H/F, vos missions seront :

 

  • Réaliser des opérations de mesure physique à l’aide de moyens de contrôle tridimensionnels tels que des machines de mesure tridimensionnelle (MMT), des laser trackers et des bras de mesure polyarticulés Faro.
  • Assurer la programmation, la validation et l’optimisation des programmes de mesure 3D, en veillant à leur performance et à leur conformité aux exigences métrologiques.
  • Référent en métrologie tridimensionnelle, vous jouez également un rôle de formateur auprès des équipes internes. À ce titre, vous accompagnez les techniciens dans la prise en main des équipements 3D et dans l’application des bonnes pratiques de mesure.
  • Elaborer et déployer les procédures de métrologie, les fiches d’instruction ainsi que les documents de suivi associés.
  • Rédiger les procès-verbaux de contrôle en analysant, interprétant et exploitant les résultats de mesure et les données statistiques.
  • Vous intervenez ponctuellement chez les fournisseurs en Europe (environ 10 % du temps), où vous réalisez des contrôles en cours de fabrication, analysez les non-conformités et rédigez les rapports associés.
Voir l'offre

Chef de Projet Industrialisation Produit Horlogerie F/H

Suisse - Genève
CDI
Ingénierie Industrielle et Life-Science

Nous recrutons en CDI un Chef de Projet Industrialisation Produit Horlogerie F/H afin de rejoindre notre pôle d'Expertise Industrielle dans le cadre d'un projet de grande envergure et longue durée, d'extension des activités de notre partenaire situé à Genève.

 

En tant que Chef de Projet Industrialisation Produit Horlogerie F/H, vos missions seront :

 

 

  • Planifier et animer les revues de convergences techniques, incluant les plans, le contrôle et les capacités des processus.
  • Élaborer et industrialiser les gammes et nomenclatures des nouveaux produits.
  • Piloter le planning des activités et gérer la levée des risques.
  • Fédérer les ressources impliquées.
  • Piloter et mettre en œuvre les évolutions des produits et des processus, en adaptant la gouvernance des séries en cours de vie.
  • Capitaliser sur les bonnes pratiques et contribuer à l’évolution des référentiels.
  • Piloter la démarche de plans modèles en lien avec les capacités de l’outil industriel.
Voir l'offre

Cloud Architect

Asia - Singapore
CDI
Conseil et Business Management

Responsibilities

  • Maintain the Division/Department architecture reference documentation all along with the changes brought by projects:
  1. IT system diagrams (Division level, or per sub-block)
  2. Application referential (with the help of Application Owners)
  3. Division level principles and related non-conformities and remediation plans
  4. Obsolescence KPIs
  • Lead the solution architecture on the projects he/she is assigned to:
  1. Supporting the Project Manager/Business Analysts during solution ideation, design, and implementation
  2. Collaborating with application teams and Business Analysts/Tech leads of impacted applications to design the solution
  3. Ensuring the alignment of projects with our architecture principles and IT standards
  4. Ensuring the solution is optimized for running on our IBM Private Cloud
  • Support project managers and tech leads along the architecture validation process by:
  1. Leading the build of a consistent architecture documentation
  2. Presenting projects in architecture validation committee
  3. Being the reference point on a set of applications for support/evolution activities
  4. Supporting the architecture process till the go-live
  5. Bringing Cloud and architecture awareness to application teams
  • Being the reference architect on a set of applications for support/evolution activities (having low architecture impacts), before and after they are migrated into the Cloud platform.
  • Collaborate with following roles:
  1. Project managers/Business analyst of major transversal projects he/she is assigned to
  2. Tech leads/Developers, to understand the architecture of the applications/screens and analyze potential issues
  3. Application owner, to update the referential information on applications
  4. Engineering and Production team, to check the availability/compatibility with infrastructure/Cloud services
  5. Enterprise Architects, to facilitate the review and validation process.
  • Ensure the reference documentation is updated all along the changes brought by projects:
  1. Application referential
  2. IT architecture diagrams and documents
  3. Application non-conformities and remediation plans
  4. Architecture principles, checklist, guidelines
  • Provide and share specific expertise on our Cloud capabilities and in selected technical areas
  • Participate in studies and proof-of-concepts with the business before a project is launched
Voir l'offre

Senior Frontend Developer - Angular

Asia - Singapore
CDI
Conseil et Business Management

We’re seeking a hands-on Software Developer to design, implement, and refine features across the product. You’ll collaborate with peers to deliver maintainable software, participate in code reviews, and mentor junior developers. You’ll also help evolve the codebase, estimate development effort, and contribute to end-to-end delivery from feature inception to production.

Key Responsibilities

  • Develop and test new features for our product, ensuring quality and maintainability.

  • Participate in constructive design discussions to deliver practical, maintainable solutions.

  • Make recommendations on how to evolve the code base to improve performance, reliability, and scalability.

  • Accurately estimate development effort and contribute to sprint planning.

  • Squash bugs promptly and implement robust fixes.

  • Participate in peer code reviews to share knowledge and ensure code quality.

  • Mentor junior developers to help grow technical capability within the team.

Functional and Transversal Competencies

  • Familiar with CI/CD of Frontend Deployment.

  • Familiar with Banking Domain (or tailor to your domain if not banking).

Voir l'offre

IT Scheduler & TWS specialist

Asia - Singapore
CDI
Conseil et Business Management

Key Responsibilities

  • TWS design and modification: Create new plans, perform impact analysis, forecast workload needs, and validate requests; maintain and evolve TWS configurations across environments (TWS, DWC, WebAdmin, framework, DB2, workstation agents).

  • Troubleshooting and incident management: Resolve Severity 1 incidents, perform cross-functional troubleshooting, escalate as needed, restore services, and perform root-cause analysis; participate in crisis management for scheduler tool incidents.

  • TWS administration: Install, configure, upgrade, maintain, and decommission TWS components; manage access rights and security; oversee obsolescence planning.

  • Service degradation response: Diagnose, log, purge, and back up scheduler data; manage logs and backups; recover from service degradation and schedule-related crises.

  • Batch server and file maintenance: Manage flat file cleanup, TSM backups, and file system health; ensure data integrity and retention policies.

  • Batch planning and system management: Coordinate batch plans during releases, DRP exercises, and environment migrations; oversee TWS and batch-related activities.

  • Projects and migrations: Lead onboarding/offboarding, site migrations, environment creation and migration (TWS, DB2, flat files); coordinate yearly FAN testing and cross-environment TWS database transfers.

  • Performance monitoring and optimization: Analyze and optimize Batch S2i and satellite performance, maintain calendars, resources, events, objects, and batch workflows.

  • Development and automation: Create shell and Python scripts, Ansible playbooks for automation; develop automated reporting and tooling to detect and resolve TWS and batch issues.

  • Documentation and governance: Maintain standard operating procedures, runbooks, and change documentation; ensure auditability and compliance.

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 communicate and work 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)