18 Medical Management jobs in Singapore

Job Responsibilities:

• Work closely with Clinical Services, Clinical Heads, other staff members of Clinical Services, internal and external stakeholders.
• Liaise with MOH and other ministry statutory boards on all hospital licensing and inspection matters.
• Coordinate and conduct Internal Hospital Quality Audit and support Quality Assurance and Clinical Services Committees.
• Provide secretariat support for Patient Record Review Committee meetings.
• Conduct audit on medical case notes to ascertain the level of completeness of clinical documentation.
• Manage Hospital Dashboard Clinical Data base (Balance score Card/ Quality Indicators).
• Ensure and maintain the roster for “Doctors On-Call” in a timely and regular manner.
• Provide oversight on document control matters, work with internal stakeholders to coordinate/work on the development or update Clinical Services’ SOPs in the hospital.
• Provide administrative and secretariat support (drafting meeting minutes) for various committees and ensure proper documentation of all meetings and follow-up.

Job Requirements:

• Experience in related areas (e.g. healthcare, clinical operations, finance) would be an advantage.
• Diploma or degree holder.
• Strong team player in a fast-pace environment with good interpersonal and communication skills (verbal and written).
• Keen eye for details.
• Adaptable, able to multi-task, work well independently and eager to learn.

Overview
Medical Doctor - Medical Services & Case Management (Singapore-based) role at Allianz Partners. This Singapore-based, non-bedside role focuses on applying medical judgment to complex, high-impact cases and championing cost-effective, evidence-based care. Partnering with global medical leadership and diverse teams, you’ll help shape decisions and pathways across local, regional, and global contexts in an office-based setting.
Note: This role will be employed under Allianz Partners Singapore (AWP Services Singapore Pte Ltd).
What You’ll Do
Case manage high-cost/complex cases, ensuring appropriate, safe, and cost-effective care
Conduct pre-authorizations for inpatient treatment and review medical claims
Lead clinical adjudication and negotiate fair, evidence-based care plans and costs
Provide internal clinical consultation to Care Operations, Underwriting, Actuarial, and Medical Provider Management (MPM) team
Build and maintain effective relationships with providers, brokers, and clients (in collaboration with MPM)
Partner with global medical decision-makers to align on best practice and outcomes
Contribute to clinical guidelines, process improvements, and knowledge sharing
Ad hoc duties aligned to the Medical Services function
Training and onboarding support will be provided. No regular travel required.
Who You Are
Medical degree with at least 2 years of clinical experience/residency (ER exposure advantageous)
Registered medical doctor; active clinical practice license not required for this role
Strong clinical judgment with the ability to balance medical appropriateness and cost-effectiveness
Healthcare insurance/assistance or managed care experience is an advantage
Negotiation skills and experience engaging with hospitals/providers are a plus
Fluent English; Mandarin and/or Cantonese are beneficial. Other languages are a plus
Proficient with Microsoft Office and comfortable with digital tools
Eligible to work in Singapore
Working pattern and location
Hybrid: 3 days in office, 2 days WFH
Work 5 days within a 7-day operation, including public holidays. Operational hours are 07:00–22:00 SGT, Monday to Sunday, with rotating shifts and two consecutive days off.
Office: AWP Services Singapore Pte Ltd, 79 Robinson Road
What Success Looks Like (6–12 Months)
Consistent delivery of safe, medically appropriate, and cost-effective case outcomes
Strong partnerships with providers and internal stakeholders; trusted clinical advisor in APAC
Visible contribution to playbooks, pre-authorization quality, and high-value claim oversight
What We Offer
Our employees play an integral part in our success as a business. We appreciate that each of our employees is unique and has unique needs and ambitions, and we enjoy being a part of their journey. We are there to empower and encourage you with your personal and professional development ensuring that you take control by offering a large variety of courses and targeted development programs. All that in a global environment where international mobility and career progression are encouraged. Caring for your health and wellbeing is a key priority for us. This is why we build Work Well programs to provide you with peace of mind and give the flexibility in planning and arranging for a better work-life balance.
If you’re excited about the role but don’t meet every single requirement, please apply—we value potential, learning agility, and diverse experiences.
Equal Opportunity
Allianz Group is committed to equal opportunities for all employees. We welcome applications regardless of ethnicity or cultural background, age, gender, nationality, religion, disability or sexual orientation, or any other characteristics protected under applicable local laws and regulations.
Join us. Let’s care for tomorrow.
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Overview
Biomedical Senior Engineer, Quality & Risk Management (Medical Devices)
Responsibilities
Implement and maintain quality management system processes across medical device innovation projects
Provide regulatory and quality guidance to project teams, including validation of unmet clinical needs, risk assessments, and de-risking of proposed solutions
Ensure compliance with quality standards, regulatory requirements, and organisational policies, supported by accurate documentation and record-keeping
Support project execution by monitoring milestones, preparing technical documentation, and ensuring alignment with grant deliverables and KPIs
Collaborate with cross-functional teams to strengthen risk and quality practices in the development of safe and effective medical technologies
Qualifications
Masters/ Bachelor Degree level in Engineering/ Science
2 - 4 years of relevant working experience preferably with hands-on in risk management processes and quality management systems for medical devices
Knowledge of ISO 13485, ISO 14971, IEC 62304; exposure to ISO 14155 and other medical device regulations/standards is an advantage
Experience with quality implementation/ maintenance and participation in ISO 13485 / IEC 62304 audits preferred
Familiarity with the software development lifecycle and technical project coordination/ documentation
Strong analytical, problem-solving, and technical writing skills
Effective communicator, team player, and highly detail-oriented
How to apply
Interested applicants, kindly furnish us with your full and detailed resume in MS Word format and click
Apply Now
button.
Disclaimers
We regret to inform only shortlisted candidates will be notified. Applicants who do not possess necessary experience or qualification will still be considered on individual merits and may be contacted for other opportunities.
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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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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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We are hiring a HR Recruiter for our organisation :)

Apply now!

What's in it for You?

- Personalized Mentorship: Experience 1-to-1 mentorship with a tailored learning scope.

Job Description:

As a vital part of our team, you'll embark on an exciting journey with responsibilities that include:

- Sourcing, evaluating, and experimenting with various recruitment methods to attract top talent through social media platforms, networking events, offline recruitment, infrastructure advertisements, and more.

- Ensuring each recruitment stage is seamlessly executed within the required time frame.

- Building and maintaining networks of potential candidates to fill future roles.

Why Choose Us:

- Educational Background: Minimum Degree

- Central Location: Work in the vibrant heart of Orchard.

- No Experience Required: On-the-job training provided.

How to Apply:

Excited to kickstart your career journey?

Interested candidates please send a copy of your resume in MS Word to:

Kennice Aw

Outsourcing Team

Recruit Express Pte Ltd, EA License No.: 99C4599

We are hiring a HR Recruiter for our organisation :)

Apply now!

What's in it for You?

- Personalized Mentorship: Experience 1-to-1 mentorship with a tailored learning scope.

Job Description:

As a vital part of our team, you'll embark on an exciting journey with responsibilities that include:

- Sourcing, evaluating, and experimenting with various recruitment methods to attract top talent through social media platforms, networking events, offline recruitment, infrastructure advertisements, and more.

- Ensuring each recruitment stage is seamlessly executed within the required time frame.

- Building and maintaining networks of potential candidates to fill future roles.

Why Choose Us:

- Educational Background: Minimum Degree

- No Experience Required: On-the-job training provided.

How to Apply:

Excited to kickstart your career journey?

Interested candidates please send a copy of your resume in MS Word to:

Kennice Aw

Outsourcing Team

Recruit Express Pte Ltd, EA License No.: 99C4599

We regret to inform that only suitable candidates will be shortlisted for an interview.

We are hiring a HR Recruiter for our organisation :)

Apply now!

What's in it for You?

- Personalized Mentorship: Experience 1-to-1 mentorship with a tailored learning scope.

Job Description:

As a vital part of our team, you'll embark on an exciting journey with responsibilities that include:

- Sourcing, evaluating, and experimenting with various recruitment methods to attract top talent through social media platforms, networking events, offline recruitment, infrastructure advertisements, and more.

- Ensuring each recruitment stage is seamlessly executed within the required time frame.

- Building and maintaining networks of potential candidates to fill future roles.

Why Choose Us:

- Educational Background: Minimum Degree

- No Experience Required: On-the-job training provided.

How to Apply:

Excited to kickstart your career journey?

Interested candidates please send a copy of your resume in MS Word to:

Kennice Aw

Outsourcing Team

Recruit Express Pte Ltd, EA License No.: 99C4599

Deployed in the Medical Report Unit, you will provide prompt operational and administrative support in processing medical report requests. You are expected to respond to public enquiries and feedback professionally regarding medical report applications. You will need to demonstrate excellent customer service skills and strong ability to manage complaints. Your role also includes coordination with Clinical Department Administration and doctors to ensure medical reports are provided accurately and in a timely manner.
Requirements
Diploma level with two years' working experience or Higher NITEC / GCE N / O / A level with eight years' working experience
Proficiency in MS Office applications (Word / Excel)
Excellent interpersonal and communication skills, including email writing
Strong organisational and coordination skills
Good customer service orientation with ability to handle complaints
Ability to work in a fast-paced environment
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