151 Medical Technology jobs in Singapore

Overview
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Medical Technology Trainee
role at
Medpace . Medpace has established laboratories in the USA, Europe, Singapore, and China. We are currently seeking a full-time Medical Technologist to join our Medpace Reference Laboratory team in Singapore. This position plays a pivotal role in research-based drug development within the pharmaceutical industry. If you have an analytical mindset and enjoy working in a laboratory setting, this could be the opportunity for you. There is potential for great career development in the clinical trial industry. The successful candidate will be trained across multi-specialties within the lab.
Responsibilities
Perform routine instrument maintenance and troubleshooting.
Develop knowledge of local and international regulations regarding clinical trials.
Develop knowledge of pre-analytical variables affecting clinical laboratory testing.
Develop knowledge of disease processes and correlation with clinical laboratory data.
Perform laboratory investigations.
Perform clinical specimen testing, documentation, and routine lab system operations.
Ensure validity of laboratory data reported.
Qualifications
Bachelor of Science degree.
Basic knowledge of drug therapy techniques and medical terminology.
Excellent written and verbal communication skills.
Able to work in a team environment with effective interpersonal skills and able to work independently.
Able to work on rotational public holidays and weekends.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients who face diseases across key therapeutic areas. The work we do today will improve the lives of people living with illness in the future.
Medpace Perks
Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives
What To Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Employment type
Full-time
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We are seeking a motivated and creative Digital Marketing Intern to support the Medical Equipment Team in driving marketing campaigns, digital engagement, and content development. This internship provides an excellent opportunity to gain hands-on experience in medical aesthetic technology marketing while working in a dynamic and fast-paced industry.
Key Responsibilities:
Support digital marketing campaigns on social media, email, and other platforms.
Help manage and update marketing materials and product content.
Conduct market research and track campaign performance.
Support event promotions such as product launches and webinars.
Key Requirements
Currently pursuing a Diploma/Degree in Marketing, Communications, Digital Media, or related field.
Interest in digital marketing and healthcare/medical aesthetics.
Familiarity with social media platforms and basic design tools (e.g., Canva, Adobe, CapCut).
Strong communication skills and eagerness to learn.
What You’ll Gain
Practical exposure to digital marketing in the medical aesthetics industry.
Guidance from experienced marketing professionals.
Opportunity to build a portfolio of impactful projects.
Monthly stipend
We provide a complimentary chartered bus service to and fro Bishan MRT taxi stand to Tagore Building at scheduled timings.
Neoasia is committed to seeking and distributing products that are clinically proven to be safe, effective and of highest quality.
Since its inception in 1995, Neoasia has been dedicated to bringing the most technologically advanced aesthetic equipment and skincare products to the medical community and consumers.
Priding itself as the setter for high standards in aesthetic technology, Neoasia recognizes the need for aesthetics practitioners to maintain their art at its peak. Combining cutting-edge technologies with exceptional relationships and premier services, Neoasia continues to keep their clients at the forefront of aesthetic trends, keeping their fingers on the pulse of global aesthetic market and bringing only the finest technologies that ensure safety and optimal results, all through science.
Neoasia's corporate headquarter is situated in Singapore, with our distribution networks extended to Malaysia, Brunei, Indonesia, Vietnam, The Philippines and China. Our secured geographical coverage of clinics, hospitals and retail outlets in the region is your guarantee to greater distribution and marketing services.
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Principal / Senior Engineer, Innovation (Quality & Risk Management), Medical Technology Office
Job Category: Administration
Posting Date: 13 Sept 2025
You will assist to establish processes and work in a team to implement risk management best practices in innovation projects aimed at adoption and commercialisation. You will implement and maintain the office's ISO 13485 and IEC 62304-compliant quality management system processes and procedures across departmental work and projects.
Your technical responsibilities include providing guidance and development support to ongoing medical technology projects. This encompasses validating unmet clinical needs, advising project teams on regulatory, quality and risk requirements, performing risk assessments of proposed solutions with consideration of regulatory requirements, and conducting clinical need filtering and de-risking.
You will ensure compliance with quality, regulatory and organisational policies and systems while supporting required record-keeping and documentation. Managing project tasks includes recommending grants, ensuring timely completion of project milestones for successful grant applications, and meeting KPIs set by the grant agency and manager.
This role combines project coordination, quality management system implementation, risk assessment and technical writing. It is ideally suited for candidates with experience or strong interest in supporting medical device innovations in the healthcare industry.
Job Requirements
Bachelor’s or Master’s Degree in Engineering or Science with minimum 2 years’ experience in quality management systems, risk management processes, and/or design and development of medical devices
Experience in risk management processes for medical technology development
Experience in implementation/maintenance of a quality management system
Experience in ISO13485 / IEC62304 audit is highly advantageous
Experience in the software development lifecycle is highly advantageous
Experience in project coordination, technical project management, and/or technical documentation implementation/maintenance is desirable
Familiarity with ISO 13485, ISO 14971, IEC 62304, ISO14155, Medical Device Regulatory, Medical Device Standards, Risk Management for Medical Devices
Strong verbal and written communication skills with proven teamwork abilities
Strong problem-solving skills and technical writing skills
Meticulous, detail-oriented, responsible and self-motivated
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Reporting to the Assistant Director, you will execute administrative and operational activities that are critical to the operation of Internet of Medical Things (IoMT) activities for medical devices at one of SingHealth's institutions and coordinate and support cybersecurity strategies. You will collate and analyse information to facilitate management decisions and prepare reports for stakeholders. You will also work with the Biomedical Engineering (BME) shared services and IT security teams across SingHealth to ensure a robust risk management framework is in place for medical devices that are connected to the IT network. This includes updating the asset inventory, implementing the relevant standards and procedures for IoMT medical devices and evaluating and executing work instructions to minimise the risk for medical devices and systems. You will also provide secretariat support and participate in ad hoc projects.

Job Requirements

• Bachelor's Degree in Computer Engineering, Computer Science, Information Technology, Electrical Engineering or equivalent are preferred. Degree holders with a recognised Diploma in Cybersecurity/IT will also be considered
• At least 6 years of relevant working experience in the area of IT, Operations and Risk Management with medical devices/systems understanding
• Good understanding of both IT and BME processes/operations and the relationship between them is an advantage
• Good working knowledge of the best practices in mitigating security risks for IoMT medical devices/systems
• Experience in healthcare facilities projects and/or government projects will be an added advantage
• Possess strong communication, administrative, organisational and management skills
• Reliable team player, independent and committed

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Senior / Manager, Medical Device Technology
Job Category: Administration
Posting Date: 31 Jul 2025
Job Description
Reporting to the Assistant Director, you will execute administrative and operational activities that are critical to the operation of Internet of Medical Things (IoMT) activities for medical devices at one of SingHealth’s institutions and coordinate and support cybersecurity strategies. You will collate and analyse information to facilitate management decisions and prepare reports for stakeholders. You will also work with the Biomedical Engineering (BME) shared services and IT security teams across SingHealth to ensure a robust risk management framework is in place for medical devices that are connected to the IT network. This includes updating the asset inventory, implementing the relevant standards and procedures for IoMT medical devices and evaluating and executing work instructions to minimise the risk for medical devices and systems. You will also provide secretariat support and participate in ad hoc projects.
Job Requirements
Bachelor’s Degree in Computer Engineering, Computer Science, Information Technology, Electrical Engineering or equivalent are preferred. Degree holders with a recognised Diploma in Cybersecurity/IT will also be considered
At least 6 years of relevant working experience in the area of IT, Operations and Risk Management with medical devices/systems understanding
Good understanding of both IT and BME processes/operations and the relationship between them is an advantage
Good working knowledge of the best practices in mitigating security risks for IoMT medical devices/systems
Experience in healthcare facilities projects and/or government projects will be an added advantage
Possess strong communication, administrative, organisational and management skills
Reliable team player, independent and committed
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Manufacturing Engineer (Medical Equipment)
Manufacturing Engineer (Medical) will be responsible for planning, designing, implementing, and managing integrated production and service delivery systems that assure performance, reliability, maintainability, schedule adherence and cost control within the production site. The Manufacturing Engineer will adopt as its goals profitability, effectiveness, adaptability, responsiveness, quality, and continuous improvement of products and services throughout their life cycles.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Capable of performing High-Level Assembly (HLA) processes. Develop procedures for these processes and train staff accordingly.
Strong Knowledge in Healthcare business with ISO 13485 & FDA regulatory would be added advantage.
Proficient in understanding and interpreting assembly drawings, part drawings, and specifications. Knowledge of medical product assembly is a plus.
Skilled in report writing, conducting Design for Manufacturability (DFM) analyses, and effectively communicating with internal and external stakeholders.
Strong understanding of PFMEA, process flow, control plans, and process risk assessments.
Maintain frequent communication with operations, technical, and quality representatives within the support area through the tier process.
Provide leadership and commitment to continuous improvements in quality, productivity, and delivery performance by deploying a continuous improvement framework.
Review all input from the Engineering Department, including Engineering Change Orders (ECOs), new product releases, configuration control policies, and marking requirements, and participate in the DFM process.
Solid understanding of Bill of Materials (BOM), Engineering Change Notice (ECN) process, Product Change Notification (PCN), and shop floor management is a strong plus.
Monitor and continuously improve daily quality and efficiency performance for assigned areas. Familiarity with Lean Tools, such as Cycle Time, TAKT Time, and Labor Balance Ratio (LBR), as well as waste reduction, is essential.
Collaborate with R&D, New Product Development, and Quality teams to provide Design for Manufacturability guidance on new hardware.
Adhere to all safety and health regulations associated with this position, as directed by the supervisor. Comply with all procedures within the company's security policy.
REQUIREMENTS
Candidate must possess at least a Diploma, Degree, Engineering (Mechatronic/Mechanical) or equivalent. At least 5 years’ work experience in the related field is required for this position.
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Overview
Under general supervision, creates and maintains assembly instructions for the manufacturing operation. Responsible for inputting Bill of Materials (BOM) per the New Product Introduction (NPI) process, obtaining material pricing for the purchasing department and verifying completion of documentation packages.
Responsibilities
Prepares and maintains data storage on the Jabil computer network and master files per ISO standards.
Prepares and implements Engineering Change Orders (ECO’s) for manufacturing assembly instructions
Interprets customer documentation, drawings and blueprints for defining manufacturing process flow
Works with the process area and engineering to define process flow
Order stencils as needed, per stencil procedure
Updates SAP routing and production status
May assist in publishing weekly and monthly reports of department performance in accordance to established standards
May be required to work overtime
Performs other duties as assigned
Coordinates the ECO activities for the business unit and work with other appropriate personnel to resolve problems that result from ECO activity
Assists in the timely completion of ECOs through documentation, validation/approval and basic input of materials and drawing information into the SAP system
Verifies ECO documentation packages for completeness and accuracy and follow up on completed ECOs to ensure continued accuracy
Communicates ECO impact with appropriate personnel including engineering, materials and production personnel. May also interact with customer and/or supplier personnel when appropriate
Verifies system to ensure requote pricing entered in the system is accurate
Participates in special projects including SAP and other systems projects
Assists in transacting excess and obsolete inventory
Responsible for maintaining bills of material in SAP
Maintains appropriate additional documentation for process metrics
May update and maintain DOC program with current documentation
Trains lower level personnel in ECO processing and execution
May perform other duties and responsibilities as assigned
Knowledge Requirements
GMP/ ISO knowledge preferred
Knowledge of product and process design and development, materials, standardization science and applied statistics
Knowledge of project management and cost analysis preferred
Knowledge of word processing, spreadsheet analysis, data management, projects management, presentation graphics, engineering analysis and statistical software
Knowledge of information systems including but not limited to Enterprise Resource Planning (ERP), Quality Systems & Documentation Control Systems
Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
Ability to define problems, collect data, establish facts, and draw valid conclusions
Ability to operate a personal computer including using a Windows based operating system and related software
Advanced PC skills, including training and knowledge of Jabil’s software packages
Ability to write simple correspondence. Read and understand visual aid
Ability to apply common sense understanding to carry out simple one- or two-step instructions
Ability to deal with standardized situations with only occasional or no variables
Ability to read and comprehend simple instructions, short correspondence, and memos
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals
Ability to compute rate, ratio, and percent and to draw and interpret graphs
Education & Experience Requirements
Three to five years’ experience in a manufacturing environment and/or medical device industry preferred
Advance technical training in area(s) of expertise preferred
Generally requires 5 years related experience
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Overview
Salary range: $1500 - $2200
Working hours: Monday – Friday (9:00am – 6:00pm)
Working Location at Serangoon North
Excellent Welfare & Benefits
Well Established Medical Equipment Supplier Company
Training Provided
Job Scope
Perform rehabilitation equipment setup and maintenance – including drilling and painting.
Conduct equipment quality checks at onsite and offsite locations.
Support delivery of equipment.
Perform any other maintenance duties as assigned by the Supervisor.
Requirements
GCE O Level and above
0 – 2 years related experience
Candidates are encouraged to apply this position via Apply Now button with the following information in the resume:
Work experiences and job responsibilities
Current and Expected salary
Reason for leaving
Date of availability
Education background
We regret that only shortlisted candidates will be contacted.
YEOW CHANG FU (R )
EA Recruitment Pte Ltd
EA License No: 21C0492
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We are seeking a proactive and reliable Assistant Warehouse Manager to join our logistics team in Yishun. You will assist in overseeing daily warehouse operations supporting hospital equipment and supplies across Singapore. This role plays a vital part in ensuring accurate inventory management, timely order fulfillment, and smooth team coordination.

• Oversee day-to-day warehouse activities including receiving, picking, packing, and dispatching of goods.
• Supervise and coordinate the warehouse team: assign tasks, monitor performance, and ensure on-time execution.
• Enforce safety, cleanliness, and inventory control procedures in line with company standards.
• Maintain accurate records of inventory and goods movement within the Warehouse Management System (WMS) .
• Conduct and support regular stocktakes and cycle counts to ensure inventory accuracy.
• Troubleshoot and resolve operational issues such as order discrepancies, delays, or team conflicts.
• Plan and optimize space utilization for efficient warehouse layout and storage.
• Assist in training and onboarding of new warehouse staff.
• Monitor usage of equipment and coordinate preventive maintenance or repairs as needed.
• Contribute to continuous improvement initiatives to drive productivity and efficiency.
• Act as the point of contact in the absence of the Supply Chain Manager (SCM).

• Diploma in Logistics, Supply Chain Management, or a related discipline.
• 3 years of warehouse operations experience, with at least 1–2 years in a supervisory or team lead role .
• Proficient in warehouse management systems (WMS) and inventory control best practices.
• A forklift license or relevant certifications will be an added advantage.