232 Medical Technology jobs in Singapore

As a seasoned Medical Technology Project Manager, you will be responsible for the end-to-end planning and execution of cross-functional projects within the medical sector. These may include new product development, manufacturing transfers, or market launches.

The ideal candidate will have a proven track record of delivering projects on time, within scope, and budget while maintaining compliance with internal quality systems and regulatory requirements.

• Lead cross-functional teams to deliver new medical devices from concept to commercialization.
• Develop and manage detailed project plans, timelines, budgets, and risk registers.
• Navigate organizational change and evolution, embedding new operating models.

You will work closely with internal and external stakeholders to define project scope, goals, and deliverables. The ability to communicate effectively and facilitate regular project meetings is essential.

As a Project Manager, you will ensure all project documentation is completed accurately and on time. You will also monitor production and supply chain performance, implementing corrective actions as needed.

• Sustainability
• Leadership
• Risk Management
• Inventory Control
• Operational Excellence
• Project Management

We are looking for a highly motivated and organized individual who can drive project velocity, ensuring successful initial implementation of projects into production.

Experience in leveraging technology to drive data-based decisions and automation across the business is highly desirable.

The Project Lead oversees the entire lifecycle of medical technology projects, from concept to commercialization.

o Develop and manage comprehensive project plans, timelines, and budgets.

o Drive execution through all phases of the product development lifecycle (PDP/NPD), including design.

The Project Lead must possess excellent leadership skills, business acumen, and the ability to motivate and direct cross-functional teams towards a common goal. They should have a strong understanding of medical device regulations, quality systems, and industry best practices.

o Deliver high-quality medical devices that meet customer needs and exceed expectations.

The Project Leader is responsible for end-to-end planning, execution and delivery of projects across various functions within the medical technology sector. These may include new product development, internal business-driven manufacturing development, clinical studies, regulatory submissions, manufacturing transfers or market launches. The Project Leader ensures all project objectives are met on time, within scope and budget while maintaining compliance with internal quality systems and regulatory requirements.

• Lead cross-functional teams to deliver new medical devices from concept to commercialization.
• Develop and manage detailed project plans, timelines, budgets and project trackers.
• Drive execution through all phases of the product development lifecycle.
• Ensure compliance with ISO 13485, FDA QSR and other relevant standards/regulations.

• Project management skills.
• Leadership and team management skills.
• Communication and stakeholder management skills.
• Risk management and mitigation skills.
• Documentation and reporting skills.

This role offers opportunities for professional growth and development in a dynamic and innovative environment.

• Bachelor's degree in Business Administration, Engineering or related field.
• 5+ years of experience in project management or related field.
• Proven track record of delivering projects on time and within budget.

Job Highlight:

• Kaki Bukit
• Basic up to $2,500
• Work Hours: (Mon – Fri)
• Morning Shift: 7:00 AM – 3:00 PM
• Afternoon Shift: 3:00 PM – 11:00 PM
  (Monday – Friday)
• Allowances: Transport Allowance: $10/month, Shift Allowance (Afternoon Shift): 180/month

Responsibilities

• Perform production processes independently following work instructions, process descriptions, cGMP, and safety guidelines.
• Operate equipment and carry out assigned process steps within the production cell.
• Maintain a safe and clean work environment in line with 5S principles.
• Participate in continuous improvement initiatives to reduce waste and enhance efficiency.
• Ensure compliance with quality standards and contribute to a culture of quality.

Requirements

• Nitec in Engineering
• No experience required; training provided.
• Comfortable working with microscopes.

Interview Process

• Face-to-face interview to understand the role.
• Theory test on Maths and English.
• Practical test using a microscope.

Interested candidate may submit full resume to (WhatsApp - Miya) and only shortlisted candidate will be notified.

By submitting your personal data and/or resume, you give consent to collection, use and disclosure of your personal data and/or resume by the company (or its agent) for the purpose of the processing and administration by the company relating to this job application.

Kuan Mei Yang

Registration Number: R

EA License No: 06C2859 (MCI Career Services Pte Ltd)

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.

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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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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The Opportunity
This global leader in medical technology, specialising in innovative therapies for cellular and gene treatments, is looking for a Legal Counsel, Asia Pacific, to join its team in Singapore.

This regional role covers South-East Asia (SEA), Australia and New Zealand (ANZ), and other APAC markets including China.

You will be part of an organisation producing cutting-edge treatments that positively impact patient outcomes. If you’re seeking a role that blends legal expertise, compliance oversight, and strategic business partnering in a dynamic sector—this could be the next step in your career.

About the Role
You’ll be a trusted advisor to senior leadership and business teams, providing practical, solution-driven legal and compliance support. Your remit will include commercial contracts, compliance programs, data protection, cybersecurity, and strategic projects such as licensing, collaborations, investments, and M&A.

This role is ideal for a legal professional who enjoys variety, thrives in international environments, and
wants to directly influence both business growth and risk management.

Shape the legal strategy towards driving growth and innovation across APAC in a leading medtech company transforming patient care.

Regional Impact: Lead legal matters across multiple high-growth APAC markets.
Strategic: M&A, partnerships, licensing, and high-value commercial agreements.
Innovation: life-changing therapies in an ever-evolving medtech environment.

What You Will Do

• Advise on legal and compliance matters across SEA, ANZ, and other APAC markets.
• Draft, review, and negotiate a wide range of agreements (distribution, vendor, licensing, clinical
  trial, sponsorship, and more).
• Support strategic initiatives including M&A, joint ventures, and collaborations.
• Partner with business leaders to identify risks and provide commercially minded legal solutions.
• Drive compliance programs, policies, and training across the region.
• Stay on top of evolving laws and regulations and communicate business impact clearly.
• Handle regulatory interactions, audits, or investigations where needed.
• Manage and collaborate with external counsel.
• Work closely with regional and global colleagues on cross-border matters.
  

What’s On Offer

• A highly visible regional role covering diverse and fast-growing markets.
• Direct involvement in both strategic projects and day-to-day business operations.
• The chance to combine legal skills with commercial impact in the healthcare sector.
• An international, collaborative culture that values openness, integrity, and practical solutions.
• Competitive benefits.
  

What We Look For

• Law degree (Juris Doctor or equivalent) from a reputable institution.
• 5–8 years’ post-qualification experience in commercial transactions.
• At least 3 years’ experience in the medical device, pharmaceutical, or biotechnology sector.
• In-house experience within a multinational environment is highly desirable.
• Regional experience supporting South-East Asia; exposure to China is a plus.
• Strong ethics, integrity, and sound judgment.
• Ability to provide clear, business-focused advice.
• Strong drafting, negotiation, and stakeholder management skills.
• Independent, proactive, and comfortable working in fast-paced environments.
  

What’s Next

If this role excites you, please apply with your updated CV directly to this posting or to our email below.

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)

Overview
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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