88 Medical Equipment jobs in Singapore

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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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
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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A leading provider of integrated medical supply chain solutions in the ASEAN region, this company specializes in medical equipment, devices, consumables, supplies, and services. They boast an extensive distribution network that serves a wide range of healthcare institutions, including government and private hospitals, day surgery centers, specialist and primary care clinics, laboratories, and nursing homes.
25 sales offices across 6 markets in SEA
Over 1,600 employees, a team of more than 250 clinical specialists
More than 10,000 hospitals and institutions served
A portfolio of over 200 brands
The Job
Promote and sell medical equipment and consumables to Hospitals, Clinics, and Eldercare facilities.
Develop and build customer relationships and expand professional networks within the healthcare sector.
Maintain and grow the existing customer base by identifying new business opportunities.
Organize and execute seminars, exhibitions, and other marketing initiatives as assigned by the company.
Consistently achieve assigned sales targets and contribute to overall business growth.
Deliver product presentations and conduct training sessions for agency-related products, including organizing product evaluation trials and gathering user feedback to support new product development.
Prepare comprehensive quarterly reports covering market intelligence, competitive landscape, promotional activities, and evolving customer needs.
Manage the full product lifecycle across all SKUs and model variants.
Implement brand management strategies with effective product positioning and benchmarking against key competitors.
Collaborate with the Manager to develop and execute successful launch plans for new products.
Oversee and control project-related costs for accounts under your responsibility, ensuring profitability and efficient resource use.
The Talent
Diploma, preferably in Nursing / Business / Biomedical Science / Science
2 years of experience in Medical Sales industry
Good communication, presentation, and interpersonal skills
Motivated, outgoing and independent
Computer Skills with MS products (Excel, PowerPoint, Word)
Next Steps: Interested applicants, please send your updated resume to with your current and expected salary. Only shortlisted candidates will be contacted.
Contact Person: Gillian Yoong, EA Licence No. 91C2918, Personnel Reg No: R , Direct Line:
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Retail Sales Executive

• Working Location: Orchard
• Working Days & Hours: 44 hours / Week
• Salary Range: $2500- $2800 + Commission

Key Responsibilities:

• Engage and guide walk-in customers in a friendly, patient manner

• Share product knowledge

• Explain the benefits of electric potential therapy and wellness tools

• Support team sales goals

• Provide excellent after-sales service

• Work closely with your team on marketing campaigns and in-store experiences

Requirements:

• Open to work on Full Shifts, weekends and public holidays
• Training Provided

Interested applicants may click apply or send your resume via WA to # (Liora) for faster response :)

Chow Zi Xin | EA R

The Supreme HR Advisory | Reg No: 14C7279

Safety Officer cum Drafter
Work Sites: Hospitals, Clinics, Nursing Homes
Full-Time | Up to $2,700 + AWS
Your Key Responsibilities:
Ensure full compliance with safety rules, SOPs, and site instructions
Act as Site Incident Controller (SIC) during emergency situations
Prepare Risk Assessments and Method Statements (RAMS)
Conduct monthly safety orientation briefings for technical staff
Draft and update project drawings using AutoCAD
Support site coordination, PM, and installation work (advantageous)
What You Bring: Advanced Certificate in Workplace Safety and Health (Level B or higher) – Mandatory
1-2 years’ experience in site safety coordination
Proficient in AutoCAD and MS Office
Experience in WICA claims handling (advantageous)
Benefits & Perks: Transport Reimbursement
from office to client sites 6-month probation period
with training and certification provided Vaccination & Safety Courses
required for site access (reimbursed after probation)
Company-Provided
Medical Insurance
& Panel Clinics Annual Medical Screening
(claim up to $00/year after 1 year) Dental Benefits
(claim up to 250/year after 1 year) Annual Leave
starting from 12 days (1-3 years)
Note:
Early termination during or shortly after probation may require reimbursement of initial costs (vaccinations, uniforms, safety courses, boots, etc.)
Ready to Take the Next Step?
If you’re passionate about safety, skilled in AutoCAD, and eager to make a real-world impact in healthcare environments — we want to hear from you.
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Clinical Support Specialist | Medical Equipment | Travel Around
Interested applicants can also send your resume to and allow our Consultant to match you with our Clients. No Charges will be incurred by Candidates for any service rendered.
WA ME @ 8882 4*** for other
Clinical Sale / Dental sales
role
Clinical Support Specialist
Salary: $3500 - $200 + Daily Allowance
Working Days & Hours: 5 Days | 9am - 6.30pm (Flexible based on clinical support nature)
Working Location: Island wide / global travel (Latam, Asean and Europe)
Reports to: Head of International Business
Position Summary
We are seeking a
Clinical Support Specialist
to provide expert support during coronary and peripheral Intravascular Lithotripsy (IVL) procedures. This field-based role combines in-procedure case support, physician and distributor training, and clinical trial facilitation. You will play a critical part in ensuring safe and effective use of our IVL platform, driving early adoption in key accounts, and gathering clinical insights to inform commercial and product strategies.
Key Responsibilities
Clinical Support & Training
Provide real-time, in-person clinical support during IVL procedures to ensure optimal use of the clinical supportsystem.
Guide clinicians through device preparation, imaging, and delivery, ensuring safe and effective technique.
Deliver comprehensive training programs to physicians, nurses, cath lab staff, and field teams.
Provide remote clinical support via on-call conference calls to assist distributor teams with urgent cases.
Train and certify distributors (both online and on-site) on product use, ensuring competency in procedural support, troubleshooting, and education.
Stand by for urgent distributor-notified clinical cases, with flexible availability for case calls or travel.
Clinical Education & Therapy Development
Deliver technical presentations and conduct workshops at hospitals, clinical meetings, and distributor events.
Build and maintain strong relationships with interventionalists and cath lab staff to support early adoption and sustained usage.
Support setup and execution of local registries or observational studies, coordinating with sites on logistics, IRB submissions, and data collection.
Engage with Key Opinion Leaders (KOLs) to support protocol development, feedback, and publication efforts.
Clinical Research & Feedback Collection
Present and support clinical trial materials (e.g., study protocols, IFUs, core lab manuals, CRFs).
Support post-market clinical follow-up and data integrity monitoring at assigned sites.
Serve as liaison between users and the marketing/R&D team to collect real-world product feedback and suggestions for improvement.
Assist in documenting product performance, case reports, adverse events, and user experience insights.
Operational & Reporting
Maintain accurate records of site visits, training sessions, and case support via CRM or designated tools.
Manage expense reports, training logs, and clinical documentation in a timely manner.
Support additional strategic accounts across regions when needed.
Requirements
At least Diploma or Degree Certificate in biomedical engineering, Nursing, Life Sciences, or related field.
2 years of clinical support in interventional cardiology, radiology, vascular surgery, or cath lab environments or at least 1 year of medical device case support or clinical research experience.
Familiarity with coronary or peripheral devices such as IVL, atherectomy, PTA/PTCA, or imaging catheters.
Technically adept, with experience in console setup, catheter prep, and procedural imaging workflows.
Clinic Sales Consultant
Salary: 3000 - 3500 + Comm
Working Days: 5.5 days including weekends (Off on weekdays)
Working Hours: 9am – 6pm / 1pm
Working Location: Tanjong Pagar
Responsibilities:
Attend to daily new leads through face-to-face interaction.
Track and meet planned sales goals and report results as and when necessary.
Design and implement strategic business plans to expand the Company’s customer base and ensure strong presence.
Coordinate with marketing team on lead generation.
Provide exceptional customer service.
Maintain fantastic rapport with customers throughout their smile journey.
Assist customer payments.
Liaise with healthcare professionals and patients about treatment plans.
Oversee clinic operations and staff duties.
Perform other ad-hoc and general administrative tasks as required by the Management.
Requirements:
At least 2 years sales experience
With experience in beauty industry is a plus
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Clinical Support Specialist - Position Overview
Position details include in-procedure support for coronary and peripheral Intravascular Lithotripsy (IVL) procedures, physician and distributor training, and clinical trial facilitation. This field-based role supports safe and effective use of the IVL platform, drives early adoption in key accounts, and gathers clinical insights to inform commercial and product strategies.
Position Details
Salary: $3500 - $200 + Daily Allowance
Working Days & Hours: 5 Days | 9am - 6.30pm (Flexible based on clinical support nature)
Working Location: Island wide / global travel (Latam, Asean and Europe)
Reports to: Head of International Business
Responsibilities
Clinical Support & Training
Provide real-time, in-person clinical support during IVL procedures to ensure optimal use of the clinical support system.
Guide clinicians through device preparation, imaging, and delivery, ensuring safe and effective technique.
Deliver comprehensive training programs to physicians, nurses, cath lab staff, and field teams.
Provide remote clinical support via on-call conference calls to assist distributor teams with urgent cases.
Train and certify distributors (both online and on-site) on product use, ensuring competency in procedural support, troubleshooting, and education.
Stand by for urgent distributor-notified clinical cases, with flexible availability for case calls or travel.
Clinical Education & Therapy Development
Deliver technical presentations and conduct workshops at hospitals, clinical meetings, and distributor events.
Build and maintain strong relationships with interventionalists and cath lab staff to support early adoption and sustained usage.
Support setup and execution of local registries or observational studies, coordinating with sites on logistics, IRB submissions, and data collection.
Engage with Key Opinion Leaders (KOLs) to support protocol development, feedback, and publication efforts.
Clinical Research & Feedback Collection
Present and support clinical trial materials (e.g., study protocols, IFUs, core lab manuals, CRFs).
Support post-market clinical follow-up and data integrity monitoring at assigned sites.
Serve as liaison between users and the marketing/R&D team to collect real-world product feedback and suggestions for improvement.
Assist in documenting product performance, case reports, adverse events, and user experience insights.
Operational & Reporting
Maintain accurate records of site visits, training sessions, and case support via CRM or designated tools.
Manage expense reports, training logs, and clinical documentation in a timely manner.
Support additional strategic accounts across regions when needed.
Clinic Sales Consultant Roles
Clinic Sales Consultant — Salary: $3 00 - 3500 + Comm
Working Days: 5.5 days including weekends (Off on weekdays)
Working Hours: 9am – 6pm / 1pm (subject to scheduling)
Working Location: Tanjong Pagar
Responsibilities
Attend to daily new leads through face-to-face interaction.
Track and meet planned sales goals and report results as necessary.
Design and implement strategic business plans to expand the Company’s customer base and ensure strong presence.
Coordinate with marketing team on lead generation.
Provide exceptional customer service.
Maintain rapport with customers throughout their smile journey.
Assist customer payments.
Liaise with healthcare professionals and patients about treatment plans.
Oversee clinic operations and staff duties.
Perform other ad-hoc and general administrative tasks as required by the Management.
Requirements
At least 2 years sales experience
Experience in beauty industry is a plus
The Supreme HR Advisory Pte Ltd | 14C7279
Ong Boon Kiet (Travys) | R
Senior Recruitment Consultant
WA ME
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Work Sites: Hospitals, Clinics, Nursing Homes
Full-Time | Up to $2,700 + AWS

Ensure full compliance with safety rules, SOPs, and site instructions
Act as Site Incident Controller (SIC) during emergency situations
Prepare Risk Assessments and Method Statements (RAMS)
Conduct monthly safety orientation briefings for technical staff
Draft and update project drawings using AutoCAD
Support site coordination, PM, and installation work (advantageous)

️ Advanced Certificate in Workplace Safety and Health (Level B or higher) – Mandatory

️ 1-2 years’ experience in site safety coordination
️ Proficient in AutoCAD and MS Office
️ Experience in WICA claims handling (advantageous)

Benefits & Perks:

️ Transport Reimbursement from office to client sites
️ 6-month probation period with training and certification provided
️ Vaccination & Safety Courses required for site access (reimbursed after probation)
️ Company-Provided Medical Insurance & Panel Clinics
️ Annual Medical Screening (claim up to $00/year after 1 year)
️ Dental Benefits (claim up to $2 0/year after 1 year)
️ Annual Leave starting from 12 days (1-3 years)
Note: Early termination during or shortly after probation may require reimbursement of initial costs (vaccinations, uniforms, safety courses, boots, etc.)

If you’re passionate about safety, skilled in AutoCAD, and eager to make a real-world impact in healthcare environments — we want to hear from you.