Process Engineer

Process Engineer
See all offers

Process Engineer

Asia - Singapore
Industrial Engineering and Life-Science
Permanent
9/5/2024
APPLY

About the role

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

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

Your profile

This is some text inside of a div block.

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

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

White Room Project Engineer

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

To join our teams in Geneva, we are looking for a Project Engineer in clean environments to act as the main contact for the MEF flow (melting) and guarantee control of pollution-related issues in cleanrooms.

 

The project :

  • Monitor, analyze and resolve pollution problems encountered in cleanrooms.
  • Guaranteeing the methodologies, processes, audits and best practices applied to clean environments, storage areas and transfers upstream of cleanrooms.
  • Conduct audits, provide coaching and make recommendations on best practices (handling, logistics, packaging).
  • Analyze existing standards and guarantee their reliability over time.
  • Characterize part cleanliness according to process requirements.
  • Manage MEF flow performance indicators.
  • Make proposals to improve the robustness of production in the face of pollution problems.

 

See the offer

Industrial Environmental Performance Project Manager F/H

Switzerland - Geneva
Permanent
Industrial Engineering and Life-Science

We are recruiting an Industrial Environmental Performance Project Manager on a permanent contract to join our center of expertise as part of a large-scale, long-term project to expand our partner's activities.

 

As an Industrial Environmental Performance Project Manager, your responsibilities will include :

 

  • Manage the continuous improvement of equipment specifications and associated environmental and energy requirements.
  • Define the objectives and guide the strategy of industrial equipment acquisition projects.
  • Integrate, promote and mobilize eco-design principles in the development of new industrial equipment.
  • On priority projects, drive the achievement of environmental objectives, from drafting specifications to industrial qualification, by bringing together all stakeholders.
  • Evaluate concepts, validate proposed technical solutions and contribute to key project decisions.
  • Organize the capitalization and valorization of environmental data in dedicated IT systems.
  • Participate in internal skills networks and cross-functional groups.
  • Communicate proactively and appropriately with our various contacts.
See the offer

Electronics Hardware/Software Test & Development Engineer M/F

Switzerland - Neuchâtel
Permanent
Industrial Engineering and Life-Science

We are recruiting a Hardware/Software Electronics Test & Development Engineer on a fixed-term contract (initially) to join our industrial expertise division as part of a large-scale project to expand our partner's activities.

 

As a Hardware/Software Electronics Test & Development Engineer, your responsibilities will include :

 

Technical analysis :

  • Analyze electronic specifications provided by clients.
  • Translate specifications into complete hardware-software technical solutions for testing the defined parameters.

 

Development & integration :

  • Develop test programs in C++.
  • Transfer and develop these programs on the D10 tester.
  • Install and debug test programs.

 

Electronic design :

  • Read, understand and validate electronic schematics.
  • Participate in their design if necessary.

 

Support & coordination :

  • Provide technical support for production.
  • Train and support production staff (on new features, updates, etc.).
  • Coordinate technical activities between clients and suppliers.

 

Tracking & tracing :

  • Manage budgets, monitor costs and ensure on-time delivery.
  • Analyze production data to optimize processes.
  • Ensure full traceability of activities carried out.

 

Quality & working environment :

  • Maintain order and cleanliness in the workplace (cleanroom, equipment, etc.).
  • Actively participate in the company's continuous improvement and quality processes.

 

See the offer

HMI Developer - Industrial Sector M/F

Switzerland - Fribourg
Permanent
Industrial Engineering and Life-Science

We are recruiting a HMI Developer - Industrial Sector 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 industrial activities.

 

As a HMI Developer - Industrial Sector M/F, your tasks will be :

 

  • Design the network architecture of the equipment and its integration into the client 's infrastructure;
  • Develop, configure and commission HMI applications, reporting tools and data collection systems for assembly machines;
  • Involvement in the entire project cycle: design, development, commissioning, testing and documentation;
  • Organize, plan and monitor projects in coordination with the team and the project manager;
  • Provide technical support and carry out on-site interventions at clients sites;
  • Contribute to R&D innovation projects, particularly in data analysis and machine learning.
See the offer

Automation Engineer F/H

Switzerland - Fribourg
Permanent
Industrial Engineering and Life-Science

We are recruiting an Automation Engineer F/H on a permanent contract to join our center of expertise, as part of a large-scale, long-term project to expand our partner's industrial activities.

 

As an Automation Engineer F/H, your responsibilities will include :

 

  • Precision machine programming.
  • Assembly machine programming.
  • Participation in the various phases of the project, from design to documentation, development, commissioning and testing.
  • Planning and monitoring of project progress in collaboration with the various stakeholders and project managers.
  • Provision of technical support and participation in visits to clients.
See the offer
APPLICATION FORM
* required fields
By submitting this form, you acknowledge that you have read our website's privacy policy, which includes your rights regarding your personal data.
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Process 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 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

Your profile

This is some text inside of a div block.

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.

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)