Project Scheduler

Project Scheduler
Voir toutes les offres

Project Scheduler

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

Vos responsabilités

Job Scope

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and maintain detailed CQV schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
  • Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning, validation and qualification activities.
  • Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of CQV milestones.
  • Support the development and execution of CQV strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
  • Ensure CQV activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
  • Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
  • Coordinate resource planning and availability for CQV tasks, including vendor and contractor support.
  • Maintain accurate documentation and change control records related to CQV scope.
  • Support audits and inspections by providing schedule-related documentation and insights.
  • Ad-hoc duties as assigned by Supervisor.
  • Contribute to the promotion of Antaes services on top of assistance provided to client

Job Scope

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and maintain detailed CQV schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
  • Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning, validation and qualification activities.
  • Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of CQV milestones.
  • Support the development and execution of CQV strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
  • Ensure CQV activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
  • Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
  • Coordinate resource planning and availability for CQV tasks, including vendor and contractor support.
  • Maintain accurate documentation and change control records related to CQV scope.
  • Support audits and inspections by providing schedule-related documentation and insights.
  • Ad-hoc duties as assigned by Supervisor.
  • Contribute to the promotion of Antaes services on top of assistance provided to client

Votre profil

This is some text inside of a div block.

Job Requirements

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • Minimum 3 years of experience in project planning within a GMP-regulated pharmaceutical environment.
  • Strong understanding of CQV processes and lifecycle documentation (URS, DQ, IQ, OQ, PQ).
  • Proficiency in project scheduling software (Primavera P6, MS Project, etc.).
  • Familiarity with ISPE Baseline Guides and industry best practices for CQV.
  • Excellent communication, organizational, and stakeholder management skills.

Good to have:

  • PMP or equivalent project management certification.
  • Experience with large-scale pharmaceutical capital projects (e.g., new facility builds, equipment upgrades).
  • Knowledge of computerized systems validation (CSV) and data integrity principles.
  • Experience with digital validation platforms (e.g. KNEAT) or eQMS systems.

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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Asia - Singapore
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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.
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  • Contribute to the promotion of Antaes services on top of assistance provided to clients
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Asia - Singapore
CDI
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  • Contribute to Life Science projects for Antaes Asia clients
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  • Troubleshoot mechanical/electrical issues to minimize equipment downtime and support uninterrupted production.
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  • Create and update Bill of Materials (BOMs), spare parts lists, and maintenance documentation in CMMS/ERP systems.
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  • 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.
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  • 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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Project Scheduler

Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI

Vos responsabilités

This is some text inside of a div block.

Job Scope

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and maintain detailed CQV schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
  • Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning, validation and qualification activities.
  • Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of CQV milestones.
  • Support the development and execution of CQV strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
  • Ensure CQV activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
  • Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
  • Coordinate resource planning and availability for CQV tasks, including vendor and contractor support.
  • Maintain accurate documentation and change control records related to CQV scope.
  • Support audits and inspections by providing schedule-related documentation and insights.
  • Ad-hoc duties as assigned by Supervisor.
  • Contribute to the promotion of Antaes services on top of assistance provided to client

Votre profil

This is some text inside of a div block.

Job Requirements

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • Minimum 3 years of experience in project planning within a GMP-regulated pharmaceutical environment.
  • Strong understanding of CQV processes and lifecycle documentation (URS, DQ, IQ, OQ, PQ).
  • Proficiency in project scheduling software (Primavera P6, MS Project, etc.).
  • Familiarity with ISPE Baseline Guides and industry best practices for CQV.
  • Excellent communication, organizational, and stakeholder management skills.

Good to have:

  • PMP or equivalent project management certification.
  • Experience with large-scale pharmaceutical capital projects (e.g., new facility builds, equipment upgrades).
  • Knowledge of computerized systems validation (CSV) and data integrity principles.
  • Experience with digital validation platforms (e.g. KNEAT) or eQMS systems.
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)