Process Engineer
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Process Engineer
Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI
8/7/2024
Partager
POSTULER
Vos responsabilités
Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Perform and review process engineering drawings and calculations, including but not limited to (heat exchanger sizing, pump selection, piping design, control valve sizing, heat and mass balances, and other engineered calculations).
- Verify and validate calculations provided by vendors, clients, and other consultants to ensure accuracy and compliance with industry standards.
- Prepare and review technical data sheets for various equipment, instrumentation, and systems used in biologics manufacturing.
- Ensure all documentation aligns with the project’s technical requirements and industry best practices.
- Support the preparation and review of risk assessments, including Hazard and Operability Studies (HAZOPs), to identify and mitigate potential risks in the process design and operation.
- Collaborate in the preparation and review of automation sequences required for process automation, ensuring seamless integration with existing systems and compliance with regulatory requirements.
- Work closely with other engineering disciplines and cross-functional departments such as automation engineering, facilities engineering, validation, project management, operations, quality, and safety.
- Facilitate effective communication and coordination to ensure project success and alignment with overall business goals.
- Review Commissioning Project Plans, Validation Project Plans, Design Qualifications, Traceability Matrices, Commissioning Protocols, Qualification Protocols, and Validation Protocols for pharmaceutical equipment and systems.
- Ensure that all client process equipment and facilities operate as intended to meet biopharmaceutical manufacturing requirements.
- Provide ongoing support to the client’s plant operations, ensuring that engineering projects align with the changing needs of the business.
- Manage upstream and downstream equipment, as well as other unit operations, to optimize production efficiency and product quality.
- Implement projects addressing Corrective Actions/Preventative Actions (CAPA) identified during deviation investigations, requests from value stream stakeholders, or GMP audits.
- Offer on-the-floor troubleshooting support for manufacturing operations, with a focus on resolving equipment-related issues.
- Raise and lead GMP change requests for implementing changes to equipment and facilities, ensuring compliance with Good Manufacturing Practices (GMP).
- Adhere to all applicable Environmental, Health, and Safety (EHS) requirements, ensuring that engineering activities support a safe and compliant workplace.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Votre profil
Job Requirements:
- Bachelor’s Degree in Biomedical Engineering, Biotechnology, Science or equivalent
- Minimum 2+ years of pharmaceutical, biopharmaceutical experience in Process Engineering and/ or Compliance (GxP) environment
- Ability to quickly know products and processes in order to assess quality issues
- 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
- Demonstrated good knowledge of technical drawings, general arrangement drawings, and equipment design drawings (P&ID) is required.
- Experience in the design and operation of biopharmaceutical manufacturing equipment and facilities.
- Experience in the management and coordination of engineering and construction management consultants, equipment vendors and contractors.
- Excellent communication skills, both written and verbal, in English
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 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.
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- 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.
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Project Manager – Equipment Design
We are looking for a proactive and detail-oriented Project Manager in Equipment Design to lead the development, design, and implementation of process equipment within a regulated environment. You will oversee technical design activities from concept to qualification, ensuring compliance with engineering standards, project timelines, and GMP requirements.
Your role:
- Lead equipment design projects from feasibility through to commissioning and qualification.
- Coordinate mechanical, automation, and process design activities with internal and external stakeholders.
- Develop and review technical specifications, design documentation, and FAT/SAT protocols.
- Manage supplier relationships, including technical alignment, design reviews, and project follow-up.
- Ensure budget and schedule control across all project phases.
- Oversee change management and risk assessment related to equipment design and modifications.
- Support CQV teams during qualification phases and participate in design improvement workshops.
- Guarantee compliance with GMP, safety, and quality standards for all equipment.
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Process Engineer
Asia - Singapore
Ingénierie Industrielle et Life-Science
CDI
Vos responsabilités
Job Description:
- Contribute to Life Science projects for Antaes Asia clients
- Perform and review process engineering drawings and calculations, including but not limited to (heat exchanger sizing, pump selection, piping design, control valve sizing, heat and mass balances, and other engineered calculations).
- Verify and validate calculations provided by vendors, clients, and other consultants to ensure accuracy and compliance with industry standards.
- Prepare and review technical data sheets for various equipment, instrumentation, and systems used in biologics manufacturing.
- Ensure all documentation aligns with the project’s technical requirements and industry best practices.
- Support the preparation and review of risk assessments, including Hazard and Operability Studies (HAZOPs), to identify and mitigate potential risks in the process design and operation.
- Collaborate in the preparation and review of automation sequences required for process automation, ensuring seamless integration with existing systems and compliance with regulatory requirements.
- Work closely with other engineering disciplines and cross-functional departments such as automation engineering, facilities engineering, validation, project management, operations, quality, and safety.
- Facilitate effective communication and coordination to ensure project success and alignment with overall business goals.
- Review Commissioning Project Plans, Validation Project Plans, Design Qualifications, Traceability Matrices, Commissioning Protocols, Qualification Protocols, and Validation Protocols for pharmaceutical equipment and systems.
- Ensure that all client process equipment and facilities operate as intended to meet biopharmaceutical manufacturing requirements.
- Provide ongoing support to the client’s plant operations, ensuring that engineering projects align with the changing needs of the business.
- Manage upstream and downstream equipment, as well as other unit operations, to optimize production efficiency and product quality.
- Implement projects addressing Corrective Actions/Preventative Actions (CAPA) identified during deviation investigations, requests from value stream stakeholders, or GMP audits.
- Offer on-the-floor troubleshooting support for manufacturing operations, with a focus on resolving equipment-related issues.
- Raise and lead GMP change requests for implementing changes to equipment and facilities, ensuring compliance with Good Manufacturing Practices (GMP).
- Adhere to all applicable Environmental, Health, and Safety (EHS) requirements, ensuring that engineering activities support a safe and compliant workplace.
- Contribute to the promotion of Antaes services on top of assistance provided to clients
Votre profil
Job Requirements:
- Bachelor’s Degree in Biomedical Engineering, Biotechnology, Science or equivalent
- Minimum 2+ years of pharmaceutical, biopharmaceutical experience in Process Engineering and/ or Compliance (GxP) environment
- Ability to quickly know products and processes in order to assess quality issues
- 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
- Demonstrated good knowledge of technical drawings, general arrangement drawings, and equipment design drawings (P&ID) is required.
- Experience in the design and operation of biopharmaceutical manufacturing equipment and facilities.
- Experience in the management and coordination of engineering and construction management consultants, equipment vendors and contractors.
- Excellent communication skills, both written and verbal, in English
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)
