70 Becton Dickinson jobs in Singapore

The Opportunity

A global leader in advanced analytics, technology solutions, and clinical research, are seeking a dedicated Field Service Engineer to support their operations in the medical technology space.

This is a hands-on, field-based role providing critical technical support for the installation, maintenance, and troubleshooting of advanced medical and analytical instruments.

You will act as the vital link between the customer and internal support teams, ensuring equipment is fully functional and service levels exceed expectations. This is an exciting opportunity to work with cutting-edge technologies that support life sciences and healthcare advancements.

Key Responsibilities

• Deliver timely on-site technical support to customers, Field Applications Scientists/Specialists, and Territory Account Managers
• Install, upgrade, repair, and maintain complex medical and scientific instrument systems
• Maintain up-to-date knowledge using service manuals, SOPs, Field Service Bulletins, and support remote connectivity
• Manage and control service inventory to ensure first-time fix performance
• Collaborate with sales and marketing teams to support system placements, contract renewals, and promotional efforts
• Build strong relationships with key clients to support the success of their systems
• Provide resolution for technical issues while maintaining excellent customer satisfaction
• Perform qualification and validation procedures at customer sites
• Coordinate and execute new system installations, including facility readiness assessments
• Participate in team projects to support continuous improvement and innovation

Required/Preferred Qualifications

• Degree in Engineering (Electrical, Electronics, Biomedical, Mechanical, or related disciplines)
• Experience servicing medical devices or analytical/laboratory instruments
• Exposure to optics and laser-based equipment is advantageous
• Strong technical troubleshooting and problem-solving skills
• Excellent interpersonal and communication abilities
• Basic knowledge of laboratory best practices and safety protocols
• Understanding of genomics, sequencing technologies, or bioinformatics is a plus
• Customer-oriented mindset with a commitment to service excellence
• Willingness to travel for on-site support, installations, and training

What’s on offer:

• Work with advanced medical and analytical technologies
• Competitive remuneration
• Dynamic and collaborative working environment

What’s next?

If you’re looking to apply your expertise in field service within a meaningful sector, we’d love to hear from you. Apply directly with your latest CV or send to us directly at

Note: Due to the high volume of applications, we may not be able to respond to everyone individually. If you do not hear from us, please assume your application was unsuccessful this time, but we encourage you to reapply in the future.

We look forward to considering your application!

Engage Group Life Science – Singapore & SEA


Engage Group Pte.Ltd is a licensed business under the Ministry of Manpower: (EA: 18C9316)

The Opportunity

A global leader in advanced analytics, technology solutions, and clinical research, are seeking a dedicated Field Service Engineer to support their operations in the medical technology space.

This is a hands-on, field-based role providing critical technical support for the installation, maintenance, and troubleshooting of advanced medical and analytical instruments.

You will act as the vital link between the customer and internal support teams, ensuring equipment is fully functional and service levels exceed expectations. This is an exciting opportunity to work with cutting-edge technologies that support life sciences and healthcare advancements.

Key Responsibilities

• Deliver timely on-site technical support to customers, Field Applications Scientists/Specialists, and Territory Account Managers
• Install, upgrade, repair, and maintain complex medical and scientific instrument systems
• Maintain up-to-date knowledge using service manuals, SOPs, Field Service Bulletins, and support remote connectivity
• Manage and control service inventory to ensure first-time fix performance
• Collaborate with sales and marketing teams to support system placements, contract renewals, and promotional efforts
• Build strong relationships with key clients to support the success of their systems
• Provide resolution for technical issues while maintaining excellent customer satisfaction
• Perform qualification and validation procedures at customer sites
• Coordinate and execute new system installations, including facility readiness assessments
• Participate in team projects to support continuous improvement and innovation

Required/Preferred Qualifications

• Degree in Engineering (Electrical, Electronics, Biomedical, Mechanical, or related disciplines)
• Experience servicing medical devices or analytical/laboratory instruments
• Exposure to optics and laser-based equipment is advantageous
• Strong technical troubleshooting and problem-solving skills
• Excellent interpersonal and communication abilities
• Basic knowledge of laboratory best practices and safety protocols
• Understanding of genomics, sequencing technologies, or bioinformatics is a plus
• Customer-oriented mindset with a commitment to service excellence
• Willingness to travel for on-site support, installations, and training

What’s on offer:

• Work with advanced medical and analytical technologies
• Competitive remuneration
• Dynamic and collaborative working environment

What’s next?

If you’re looking to apply your expertise in field service within a meaningful sector, we’d love to hear from you. Apply directly with your latest CV or send to us directly at

Note: Due to the high volume of applications, we may not be able to respond to everyone individually. If you do not hear from us, please assume your application was unsuccessful this time, but we encourage you to reapply in the future.

We look forward to considering your application!

Engage Group Life Science – Singapore & SEA


Engage Group Pte.Ltd is a licensed business under the Ministry of Manpower: (EA: 18C9316)

The Opportunity

A global leader in advanced analytics, technology solutions, and clinical research, are seeking a dedicated Field Service Engineer to support their operations in the medical technology space.

This is a hands-on, field-based role providing critical technical support for the installation, maintenance, and troubleshooting of advanced medical and analytical instruments.

You will act as the vital link between the customer and internal support teams, ensuring equipment is fully functional and service levels exceed expectations. This is an exciting opportunity to work with cutting-edge technologies that support life sciences and healthcare advancements.

Key Responsibilities

• Deliver timely on-site technical support to customers, Field Applications Scientists/Specialists, and Territory Account Managers
• Install, upgrade, repair, and maintain complex medical and scientific instrument systems
• Maintain up-to-date knowledge using service manuals, SOPs, Field Service Bulletins, and support remote connectivity
• Manage and control service inventory to ensure first-time fix performance
• Collaborate with sales and marketing teams to support system placements, contract renewals, and promotional efforts
• Build strong relationships with key clients to support the success of their systems
• Provide resolution for technical issues while maintaining excellent customer satisfaction
• Perform qualification and validation procedures at customer sites
• Coordinate and execute new system installations, including facility readiness assessments
• Participate in team projects to support continuous improvement and innovation

Required/Preferred Qualifications

• Degree in Engineering (Electrical, Electronics, Biomedical, Mechanical, or related disciplines)
• Experience servicing medical devices or analytical/laboratory instruments
• Exposure to optics and laser-based equipment is advantageous
• Strong technical troubleshooting and problem-solving skills
• Excellent interpersonal and communication abilities
• Basic knowledge of laboratory best practices and safety protocols
• Understanding of genomics, sequencing technologies, or bioinformatics is a plus
• Customer-oriented mindset with a commitment to service excellence
• Willingness to travel for on-site support, installations, and training

What's on offer:

• Work with advanced medical and analytical technologies
• Competitive remuneration
• Dynamic and collaborative working environment

What's next?

If you're looking to apply your expertise in field service within a meaningful sector, we'd love to hear from you. Apply directly with your latest CV or send to us directly at

Note: Due to the high volume of applications, we may not be able to respond to everyone individually. If you do not hear from us, please assume your application was unsuccessful this time, but we encourage you to reapply in the future.

We look forward to considering your application

Engage Group Life Science – Singapore & SEA



Engage Group Pte.Ltd is a licensed business under the Ministry of Manpower: (EA: 18C9316)

Field Service Engineer

We are seeking a skilled Field Service Engineer to support our medical technology operations. As a key member of our team, you will deliver timely on-site technical support to customers and internal teams, ensuring equipment is fully functional and service levels exceed expectations.

• Deliver timely on-site technical support to customers and internal teams.
• Install, upgrade, repair, and maintain complex medical and scientific instrument systems.

To be successful in this role, you must have:

• A degree in Engineering (Electrical, Electronics, Biomedical, Mechanical, or related disciplines).
• Experience servicing medical devices or analytical/laboratory instruments.
• Strong technical troubleshooting and problem-solving skills.
• Excellent interpersonal and communication abilities.

In return for your expertise, we offer:

• The opportunity to work with advanced medical and analytical technologies.

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Job Category: Administration

Posting Date: 2 Aug 2025

You will assist in the identification, validation and selection of unmet clinical needs, as well as participate in solution generation and prototyping. You will conduct testing, create supporting documentation required for patenting and regulatory approval and work with partners on commercialisation strategy.

You will coordinate and compile relevant information for grants and other funding applications, as well as manage and drive project tasks to ensure timely completion of project milestones. You will create relevant documentation, meeting records and support follow-up actions for clinical innovation projects.

You will support the device development team in brainstorming and prototype creation for projects. You will also be involved in general administrative and procurement assistance, and support the department in the program management of med-tech innovation grants including the grant application process, grant award and progress reporting.

You will provide administrative support for innovation training and education initiatives, including planning, implementation, publicity and events.

You will ensure compliance with quality, regulatory and organisation policies and systems, and support record-keeping and documentation needed for compliance.

Requirements

• Master’s / Bachelor’s Degree in Engineering, Biomedical Engineering or Science with preferably 2 years’ experience in medical technology innovation leading the development of concept ideas into products.
• Excellent team work and communication skills.
• Excellent problem solving skills with strong focus in technical writing.
• Strong knowledge in IT, CAD and/or Simulation Skills, e.g. LabView, MatLab, SolidWorks, AutoCad.
• Good knowledge in ISO 13485, ISO14155, Good Clinical Practice (GCP), Regulatory Affairs, Medical Device Standards, Intellectual Property Strategy will be an advantage.
• Knowledge of trial procedures, institutional, Centralised Institutional Review Board and regulatory authority (HSA) requirements will be an advantage.

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Senior / Engineer, Innovation, Medical Technology Office

Job Category: Administration

Posting Date: 2 Aug 2025

You will assist in the identification, validation and selection of unmet clinical needs, as well as participate in solution generation and prototyping. You will conduct testing, create supporting documentation required for patenting and regulatory approval and work with partners on commercialisation strategy.

You will coordinate and compile relevant information for grants and other funding applications, as well as manage and drive project tasks to ensure timely completion of project milestones. You will create relevant documentation, meeting records and support follow-up actions for clinical innovation projects.

You will support the device development team in brainstorming and prototype creation for projects. You will also be involved in general administrative and procurement assistance, and support the department in the program management of med-tech innovation grants including the grant application process, grant award and progress reporting.

You will provide administrative support for innovation training and education initiatives, including planning, implementation, publicity and events.

You will ensure compliance with quality, regulatory and organisation policies and systems, and support record-keeping and documentation needed for compliance.

Requirements

• Master’s / Bachelor’s Degree in Engineering, Biomedical Engineering or Science with preferably 2 years’ experience in medical technology innovation leading the development of concept ideas into products.
• Excellent team work and communication skills.
• Excellent problem solving skills with strong focus in technical writing.
• Strong knowledge in IT, CAD and/or Simulation Skills, e.g. LabView, MatLab, SolidWorks, AutoCad.
• Good knowledge in ISO 13485, ISO14155, Good Clinical Practice (GCP), Regulatory Affairs, Medical Device Standards, Intellectual Property Strategy will be an advantage.
• Knowledge of trial procedures, institutional, Centralised Institutional Review Board and regulatory authority (HSA) requirements will be an advantage.

The Agency for Care Effectiveness (ACE) is a Health Technology Assessment (HTA) entity within MOH. The role of ACE is to a) support national policy decision making through evidence-based assessments and appraisals; b) produce national Guidance on appropriate, clinical and cost-effective patient care; and c) design and deliver interventions to ensure maximum value for the system and patients.

As a Analyst/Specialist you will be responsible for a) conducting HTA or horizon scanning assessments by collating, analysing and synthesising qualitative and quantitative evidence; b) developing Guidance and other outputs informed by evidence-based decision-making; c) developing negotiation strategies to achieve fair prices for medical technologies prior to consideration for listing into the Implant Subsidy List (ISL); d) working with stakeholders, including clinical experts and senior staff to facilitate successful implementation of recommendations and Guidance; (e) horizon scanning for new and emerging health technologies on a regular basis, and monitoring these technologies for their regulatory and developmental status.

CRITICAL ACCOUNTABILITIES

Technical evaluation

• Critically appraise published evidence on the clinical and cost effectiveness of medical technologies, its potential budget impact and organisational feasibility
• Conduct systematic reviews, meta-analysis and economic evaluations (when required) to inform decision-making using standardised methods
• Assess the completeness of the evidence base, identifying gaps and highlighting important issues for discussion
• Liaise with clinical experts and other stakeholders to better understand local clinical management of specific conditions
• Prepare evaluation reports, guidance documents and other related products for internal and external dissemination
• Analyse market trends for health technologies and generate market forecasts for medical technologies using published reports, data, and statistics
• Manage market intelligence for emerging health technologies before their local regulatory approval or in the early stages of use in the Singapore healthcare system
• Develop strategies to inform negotiations with companies based on evidence submissions, pricing proposals, and market analyses
• Draft manuscripts for publication in select journals in collaboration with key clinical experts to increase visibility of ACE’s technical evaluations

Planning & organisation

• Participate in and assist with the coordination of key internal meetings such as scoping workshops, pricing negotiation meetings, committee meetings and meetings with senior management
• In conjunction with the Senior Lead Specialist, ensure adequate operational technical capacity and resourcing for each project

Implementation & evaluation of impact

• Work with other team within ACE, other MOH divisions, and other stakeholders to ensure successful implementation of guidance and subsidy
• Support efforts to evaluate the impact of ACE guidance in terms of clinical outcomes, system impact, and costs
• Manage databases related to technologies evaluated
• Preparing and presenting structured summaries of evidence and specialist advice to ACE’s committees to facilitate discussion on possible recommendations
• Maintain links with external academic, professional and clinical institutions to ensure current best practice
• Promote technical work of ACE internationally to increase the Agency’s visibility as a centre for technical excellence in HTA
• Draft written responses to comments and queries received from stakeholders
• Develop educational collaterals and communication pieces relevant to stakeholders’ needs
• Undertake continuing personal and professional development to satisfy the required technical competencies for the role
• For Senior Specialist, supervise and mentor other more junior members of the team as needed

Commissioning & quality assurance

• Provide quality assurance for internal and externally commissioned projects conducted by team members (peer-review)
• Ensure consistency across documents produced in terms of format, content and acceptable quality
• Continually evaluate and evolve workflows to maximise efficiency

JOB REQUIREMENTS

• Bachelor’s degree in biomedical engineering, pharmacy, life sciences or related fields (recent graduates welcome)
• Post graduate qualifications in genomics, public health, epidemiology, statistics or equivalent level of knowledge acquired through research experience and further training/development is desirable
• Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research evidence
• Understanding of methodology to conduct clinical and cost-effectiveness analyses of health technologies, and produce HTA reports
• Working knowledge of all of the following areas and specialist knowledge in at least one of the following:

> Genomics

> Health economics

> Medical statistics

> Clinical trials

> Public health

> Health policy

> Systematic reviews

• Ability to gather, analyse, critique, synthesise and interpret complex information and prepare guidance documents, policy papers and briefing documents
• Experience and familiarity with databases, such as PubMed/Medline, Embase and Cochrane, and grey literature
• Familiarity with conducting internet searches of various websites including regulatory and HTA agencies, and manufacturer webpages
• Ability to anticipate the system-wide impact of recommendations to subsidise particular treatments including the impact on other hospital units, patients, and the society as a whole is desirable.
• Ability to write succinctly and translate complex technical information into plain English for different audiences
• A commitment to excellence in quality of research and outputs
• Effective organisational and time management skills with ability to prioritise work efficiently and effectively to meet deadlines
• Sensitivity to emerging technology trends and ability to conduct trend analysis to decipher the patterns of market movement
• Effective and persuasive communicator demonstrating oral, written and presentation skills with a high degree of personal credibility and sensitivity
• Ability to establish effective working relationships with a range of professionals both within and outside MOH
• Ability to think and plan strategically and to exercise sound judgement in the face of conflicting pressures
• A general understanding of the local health system and the social, political, economic and technical context within which MOH operates is desirable
• Experience working within an academic, clinical or health services research environment, or pharmaceutical or medical device company and supporting a multidisciplinary team is desirable.
• Ability to use standard Microsoft packages. Familiarity with specialist statistics and/or health economics software packages (e.g. TreeAge, STATA) is desirable
• For the Senior Specialist role, line management or mentoring experience of junior staff members is desirable.

Only shortlisted candidates will be notified

• Seniority level Mid-Senior level

• Employment type Contract

• Job function Analyst
• Industries Government Administration, Hospitals and Health Care, and Public Health

Referrals increase your chances of interviewing at Agency for Care Effectiveness (ACE) by 2x

Get notified about new Information Technology Analyst jobs in Singapore, Singapore .

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

Analyst / Specialist / Senior Specialist, Medical Technology Evaluation

Analyst / Specialist / Senior Specialist, Medical Technology Evaluation

The Agency for Care Effectiveness (ACE) is a Health Technology Assessment (HTA) entity within MOH. The role of ACE is to a) support national policy decision making through evidence-based assessments and appraisals; b) produce national Guidance on appropriate, clinical and cost-effective patient care; and c) design and deliver interventions to ensure maximum value for the system and patients.

As a Analyst/Specialist you will be responsible for a) conducting HTA or horizon scanning assessments by collating, analysing and synthesising qualitative and quantitative evidence; b) developing Guidance and other outputs informed by evidence-based decision-making; c) developing negotiation strategies to achieve fair prices for medical technologies prior to consideration for listing into the Implant Subsidy List (ISL); d) working with stakeholders, including clinical experts and senior staff to facilitate successful implementation of recommendations and Guidance; (e) horizon scanning for new and emerging health technologies on a regular basis, and monitoring these technologies for their regulatory and developmental status.

CRITICAL ACCOUNTABILITIES

Technical evaluation

• Critically appraise published evidence on the clinical and cost effectiveness of medical technologies, its potential budget impact and organisational feasibility
• Conduct systematic reviews, meta-analysis and economic evaluations (when required) to inform decision-making using standardised methods
• Assess the completeness of the evidence base, identifying gaps and highlighting important issues for discussion
• Liaise with clinical experts and other stakeholders to better understand local clinical management of specific conditions
• Prepare evaluation reports, guidance documents and other related products for internal and external dissemination
• Analyse market trends for health technologies and generate market forecasts for medical technologies using published reports, data, and statistics
• Manage market intelligence for emerging health technologies before their local regulatory approval or in the early stages of use in the Singapore healthcare system
• Develop strategies to inform negotiations with companies based on evidence submissions, pricing proposals, and market analyses
• Draft manuscripts for publication in select journals in collaboration with key clinical experts to increase visibility of ACE’s technical evaluations

Planning & organisation

• Participate in and assist with the coordination of key internal meetings such as scoping workshops, pricing negotiation meetings, committee meetings and meetings with senior management
• In conjunction with the Senior Lead Specialist, ensure adequate operational technical capacity and resourcing for each project

Implementation & evaluation of impact

• Work with other team within ACE, other MOH divisions, and other stakeholders to ensure successful implementation of guidance and subsidy
• Support efforts to evaluate the impact of ACE guidance in terms of clinical outcomes, system impact, and costs
• Manage databases related to technologies evaluated
• Preparing and presenting structured summaries of evidence and specialist advice to ACE’s committees to facilitate discussion on possible recommendations
• Maintain links with external academic, professional and clinical institutions to ensure current best practice
• Promote technical work of ACE internationally to increase the Agency’s visibility as a centre for technical excellence in HTA
• Draft written responses to comments and queries received from stakeholders
• Develop educational collaterals and communication pieces relevant to stakeholders’ needs
• Undertake continuing personal and professional development to satisfy the required technical competencies for the role
• For Senior Specialist, supervise and mentor other more junior members of the team as needed

Commissioning & quality assurance

• Provide quality assurance for internal and externally commissioned projects conducted by team members (peer-review)
• Ensure consistency across documents produced in terms of format, content and acceptable quality
• Continually evaluate and evolve workflows to maximise efficiency

JOB REQUIREMENTS

• Bachelor’s degree in biomedical engineering, pharmacy, life sciences or related fields (recent graduates welcome)
• Post graduate qualifications in genomics, public health, epidemiology, statistics or equivalent level of knowledge acquired through research experience and further training/development is desirable
• Understanding of the principles of evidence-based healthcare, critical appraisal and the interpretation and synthesis of health care research evidence
• Understanding of methodology to conduct clinical and cost-effectiveness analyses of health technologies, and produce HTA reports
• Working knowledge of all of the following areas and specialist knowledge in at least one of the following:

> Genomics

> Health economics

> Medical statistics

> Clinical trials

> Public health

> Health policy

> Systematic reviews

• Ability to gather, analyse, critique, synthesise and interpret complex information and prepare guidance documents, policy papers and briefing documents
• Experience and familiarity with databases, such as PubMed/Medline, Embase and Cochrane, and grey literature
• Familiarity with conducting internet searches of various websites including regulatory and HTA agencies, and manufacturer webpages
• Ability to anticipate the system-wide impact of recommendations to subsidise particular treatments including the impact on other hospital units, patients, and the society as a whole is desirable.
• Ability to write succinctly and translate complex technical information into plain English for different audiences
• A commitment to excellence in quality of research and outputs
• Effective organisational and time management skills with ability to prioritise work efficiently and effectively to meet deadlines
• Sensitivity to emerging technology trends and ability to conduct trend analysis to decipher the patterns of market movement
• Effective and persuasive communicator demonstrating oral, written and presentation skills with a high degree of personal credibility and sensitivity
• Ability to establish effective working relationships with a range of professionals both within and outside MOH
• Ability to think and plan strategically and to exercise sound judgement in the face of conflicting pressures
• A general understanding of the local health system and the social, political, economic and technical context within which MOH operates is desirable
• Experience working within an academic, clinical or health services research environment, or pharmaceutical or medical device company and supporting a multidisciplinary team is desirable.
• Ability to use standard Microsoft packages. Familiarity with specialist statistics and/or health economics software packages (e.g. TreeAge, STATA) is desirable
• For the Senior Specialist role, line management or mentoring experience of junior staff members is desirable.

Only shortlisted candidates will be notified

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Analyst

• Industries

  Government Administration, Hospitals and Health Care, and Public Health

Referrals increase your chances of interviewing at Agency for Care Effectiveness (ACE) by 2x

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Principal / Engineer, Innovation (Innovation Adoption), Medical Technology Office (Contract)
Job Category: Administration
Posting Date: 26 Jul 2025
As part of the innovation team, your role involves establishing processes and working to productise selected innovations including medical devices, software and AI medical devices for adoption within the SingHealth cluster. This includes collaborating with internal stakeholders and external manufacturing partners to implement these innovations in operational and clinical settings, while providing post-deployment technical support.
A key aspect of the role involves interfacing with end users and stakeholders to gather real-world implementation, clinical and cost-effectiveness data. This data supports impact assessment of adopted innovations and their eventual commercial potential. Additionally, the role encompasses defining, implementing and maintaining relevant processes and procedures under the office's ISO 13485-compliant quality management system.
Job Requirements
Bachelor’s Degree in Engineering or Science
2-4 years of relevant working experience in productisation, quality management systems, supply chain, enterprise IT and/or manufacturing
A Master’s Degree or PhD is advantageous
Experience in creating medical devices from project to marketed product
Experience in implementation/maintenance of a quality management system
Familiarity with ISO 13485, ISO 14971, IEC 62304, AI Medical Devices, Software-as-Medical-Device (SAMD), Medical Device Regulations, Medical Device Standards, Risk Management for Medical Devices
Knowledge of business or financing models for medical technology industries
Meticulous, responsible and self-motivated individual with excellent communication skills
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