150 Policy Lead jobs in Singapore

Government Affairs and Public Policy Lead, Google Cloud
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Experience driving progress, solving problems, and mentoring more junior team members; deeper expertise and applied knowledge within relevant area.
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Google will be prioritizing applicants who have a current right to work in Singapore, and do not require Google's sponsorship of a visa.
Bachelor's degree or equivalent practical experience.
7 years of experience in policy analysis and campaigns, working on technology issues or the policy environments that surround them.
7 years of experience working within government, think tanks, public interest groups, technology industry groups, or corporate public policy organizations.
Preferred qualifications:
Experience working on public policy issues in the technology industry as a trusted advisor and partner to business teams in go-to-market, product development, legal and risk/compliance.
Experience in policy and regulatory issues relating to Cloud products and services (e.g. IaaS, PaaS and SaaS products) and Technical Infrastructure (data centers, cloud regions and subsea cables).
Experience in government relations and political acumen, leading public sector outcomes and policy implementations.
Experience in government relations and public policy across multiple Asia Pacific jurisdictions and markets. Leading and executing cross-functional projects.
About the job
As a member of Google’s Government Affairs and Public Policy team, you'll be part of a global government affairs team, working across regions, product areas, and functions. You’ll combine creativity and intellectual excellence with the organizational skills to manage various campaigns, projects and initiatives. In this role, you’ll advocate for Google to bring external perspectives back into the company to inform our perception and direction. You're passionate about the opportunity to shape the future of how we use and build technology for everyone.
Google takes its responsibilities seriously, including engaging with government and other stakeholders on important public policy challenges. The Government Affairs and Public Policy (GAPP) team leads the company’s engagement with executive branch officials, legislators, regulators and third-parties in the formation of public policy. Working closely with Google leaders, GAPP seeks to identify key policy issues, listen carefully to others’ views and opinions, and distill and share the company’s perspective on those issues with external stakeholders. While we focus on challenges affecting the internet, our issue areas are increasingly broad and encompass many areas where public policy, business, and technology intersect.
Responsibilities
Develop and lead government affairs and policy initiatives to create an operating and regulatory environment for Google Cloud across markets in Asia Pacific.
Build policy debates and advocate for pro-innovation policies that advance digital transformation through cloud adoption, responsible AI development, secure cross-border data flows, digital trust and enabling regulatory frameworks.
Serve as a trusted advisor to Google Cloud leadership on policy and political matters, using government engagement and policy levers to unlock opportunities for Google Cloud in the public sector and regulated industries.
Lead policy and government engagement efforts to support the expansion of Google's Technical Infrastructure, including data centers, cloud regions, subsea cables and supply chain activities.
Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents-to-be, criminal histories consistent with legal requirements, or any other basis protected by law. See also Google's EEO Policy , Know your rights: workplace discrimination is illegal , Belonging at Google , and How we hire .
Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.
To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes.
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Working as part of the Public Policy team and under the direction of the Head of Public Policy, this role contributes to the team’s mission by researching domestic and international regulatory frameworks, developing actionable reform proposals, and identifying barriers to implementation. It helps build reform momentum through early wins, stakeholder alignment, and strategic analysis that supports the team's broader policy objectives.

JOB RESPONSIBILITIES:

Conduct Comparative Policy Research & Analysis

Conduct high-quality research comparing Cambodia’s regulatory frameworks—particularly in financial services—to those of regional peers and relevant international models.

Deliverables could include structured benchmarking reports, sector diagnostics, and comparative insight memos.

Draft Recommendations for Policy Reform

Translate research findings into specific, evidence-based reform proposals tailored to Cambodia’s legal, institutional, and market context.

Recommendations should include rationale, regional relevance, and projected impact on investment climate improvement.

Identify Barriers, Bottlenecks and Encumbrances:

Systematically identify the legal, institutional, political, and operational obstacles that may impede the adoption or implementation of proposed reforms.

Deliverables may include risk maps, stakeholder resistance assessments, and internal advisory notes on mitigation strategies

Enable Reform & Build Momentum

Identify quick wins, low-hanging policy improvements, and opportunities for coalition-building to advance reform objectives. This includes mapping allies, sequencing proposals for early success, and creating conditions for broader institutional buy-in.

JOB REQUIREMENTS:

Education & Certification:

• Bachelor’s degree required in Law , Public Policy , Economics , Political Science , or a related field.
• Master’s degree (e.g. MPP , LL.M , MA in International Affairs , or Development Economics ) is strongly preferred.
• Additional certification or training in regulatory affairs , financial regulation , or public administration is a plus.

Experiences & Skills:

• 3–6 years of relevant experience in a regulatory authority, central bank, economic think tank, policy advisory role, or international development agency.
• Demonstrated ability to analyze regulatory frameworks , benchmark global best practices, and translate findings into concrete policy recommendations .
• Familiarity with financial sector regulation , especially in fintech, banking, or capital markets, and understanding of emerging market dynamics .
• Strong analytical and research skills , with the ability to synthesize complex legal and institutional material into actionable insights.
• Excellent written and verbal communication skills , including the ability to prepare clear memos, white papers, and reform proposals for both technical and non-technical audiences.
• Experience working in multistakeholder or cross-functional environments , ideally involving government counterparts, international institutions, and internal teams.

Due to the high volume of applications, only shortlisted candidates will be contacted. Contact us at com for general inquiries.

• Seniority level Associate

• Employment type Full-time

• Job function Research, Analyst, and Consulting
• Industries Investment Management, Venture Capital and Private Equity Principals, and Real Estate

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Regulatory Affairs Lead / Policy Advisor (Based in Cambodia)

Regulatory Affairs Lead / Policy Advisor (Based in Cambodia)

Working as part of the Public Policy team and under the direction of the Head of Public Policy, this role contributes to the team’s mission by researching domestic and international regulatory frameworks, developing actionable reform proposals, and identifying barriers to implementation. It helps build reform momentum through early wins, stakeholder alignment, and strategic analysis that supports the team's broader policy objectives.

JOB RESPONSIBILITIES:

Conduct Comparative Policy Research & Analysis

Conduct high-quality research comparing Cambodia’s regulatory frameworks—particularly in financial services—to those of regional peers and relevant international models.

Deliverables could include structured benchmarking reports, sector diagnostics, and comparative insight memos.

Draft Recommendations for Policy Reform

Translate research findings into specific, evidence-based reform proposals tailored to Cambodia’s legal, institutional, and market context.

Recommendations should include rationale, regional relevance, and projected impact on investment climate improvement.

Identify Barriers, Bottlenecks and Encumbrances:

Systematically identify the legal, institutional, political, and operational obstacles that may impede the adoption or implementation of proposed reforms.

Deliverables may include risk maps, stakeholder resistance assessments, and internal advisory notes on mitigation strategies

Enable Reform & Build Momentum

Identify quick wins, low-hanging policy improvements, and opportunities for coalition-building to advance reform objectives. This includes mapping allies, sequencing proposals for early success, and creating conditions for broader institutional buy-in.

JOB REQUIREMENTS:

Education & Certification:

• Bachelor’s degree required in Law , Public Policy , Economics , Political Science , or a related field.
• Master’s degree (e.g. MPP , LL.M , MA in International Affairs , or Development Economics ) is strongly preferred.
• Additional certification or training in regulatory affairs , financial regulation , or public administration is a plus.

Experiences & Skills:

• 3–6 years of relevant experience in a regulatory authority, central bank, economic think tank, policy advisory role, or international development agency.
• Demonstrated ability to analyze regulatory frameworks , benchmark global best practices, and translate findings into concrete policy recommendations .
• Familiarity with financial sector regulation , especially in fintech, banking, or capital markets, and understanding of emerging market dynamics .
• Strong analytical and research skills , with the ability to synthesize complex legal and institutional material into actionable insights.
• Excellent written and verbal communication skills , including the ability to prepare clear memos, white papers, and reform proposals for both technical and non-technical audiences.
• Experience working in multistakeholder or cross-functional environments , ideally involving government counterparts, international institutions, and internal teams.

Due to the high volume of applications, only shortlisted candidates will be contacted. Contact us at com for general inquiries.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Consulting

• Industries

  Investment Management, Venture Capital and Private Equity Principals, and Real Estate

Referrals increase your chances of interviewing at Belt Road Capital Management by 2x

Get notified about new Policy Advisor jobs in Singapore, Singapore .

Senior/Principal Policy Officer, Economic Policy

Senior / Public Health Officer (Operations and Policy)

User Trust Policy Manager - Business Integrity

Senior/ Health Policy Analyst (Recruitment & Attraction)

Deputy Director / Assistant Director (Competition and Consumer Policy)

Analyst/Senior Analyst/Lead Analyst (Appointments & Movements), HR Policy, PSD

High Harm Policy Manager, Malaysia, Trust & Safety

Assistant Director (Policy & Compliance), Online Safety and Content Regulation

Senior Executive / Assistant Manager / Manager, Security Policy & Governance

Senior Analyst / Lead Analyst (Performance Management), HR Policy

Policy Systems (Guidances) Intern - 2025 Start

Assistant Manager / Senior Assistant Manager, Registrar's Office (Academic Policies)

Assistant Manager / Manager (Market and Spectrum Policy)

Principal Analyst - Senior Principal Analyst (Strategic & Corporate Planning/ Policy and Planning Dept)

Senior Lead Analyst (Appointments, Movements & Benefits), HR Policy

Product Policy Manager - GenAI Safety Policy

Research Analyst / Senior Analyst / Associate Research Fellow (China Programme) (RSIS)

Assistant Manager/Manager (Compliance Policy & Analytics Dept) (1 year contract)

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REGULATORY AFFAIRS - PROJECT COORDINATOR - 8 Months contract

• Duration: 8 months

• udget: Up to $6.2K

• T rget onboarding: November 2025

• L cation: north

• C ordinate regulatory projects within the IPRA team

encompassing end-to-end planning, timeline management, regulatory submissions, and cross-functional communication to ensure project milestones are met and issues are promptly resolved.

• P epare and draft essential regulatory documentation for product registration across various countries, including the generation of specification sheets for new product submissions.

• O ersee a range of operational activities including blue sheet evaluations, regulatory assessments, internal training facilitation, IPRA system initiatives, PIP registrations, and the management of licenses, product listings, and related documentation.

• C mpile and consolidate technical and managerial reports from internal departments to support timely and accurate product registration submissions.

• R view marketing materials and technical documentation to ensure alignment with APAC regulatory requirements and compliance standards.

• P rform due diligence on contractual agreements and supporting materials to safeguard intellectual property rights and uphold business interests.

• D liver secretarial and administrative support for PIP meetings, including agenda setting, documentation review, minute taking, and follow up circulation to stakeholders. Track project progress and coordinate monthly dissemination of relevant data and updates, while managing document reviews and approvals through the designated gatekeeping systems.

• P rform any additional ad-hoc or miscellaneous tasks as assigned by the manager to support team operations and project objectives.

Interested candidates, do submit your resume to: OR telegram @jocelynchan

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R1331820

Principal Task: The successful candidate will first and foremost be responsible for regulatory affairs and product registrations for all SciMed products. The candidate will be the focal point of contact for advice on regulatory guidelines and activities. Besides regulatory affairs, the candidate will also support the Management Representative in ensuring an effective Quality Management System (QMS) and local implementation of PHC's compliance policies and ensure full adherence where necessary.

1. Regulatory Affairs

• Understand relevant regulatory regulations, policies & procedures behind the company's business activities and products
• Ensure product and company's compliance with regulations for maintenance of approvals
• Maintain ISO and GDPMDS records, and work closely with the ISO/GDPMDS team to provide timely updates on company's regulatory and licensing matters
• Preparation and submission of regulatory applications, including creating and maintaining templates and ensuring completion of submissions
• Advise management on regulatory processes, compliance and updates to policies
• Responsible for the maintenance of regulatory documentation databases
• Develop and maintain communication with regulatory agencies regarding submission strategies, compliancetest requirements, potential regulatory pathways, or clarification, and follow-up on submissions and reviews quality management systemo new product(s) launch in local and/or regional markets
• Main contact point for various regulatory-related internal inquiries regarding logistics, pre/post-marketing events in addressing customers' requirements.
• Support the country managers in medical device regulations or other regulations for regional countries
• Liaise with related departments in the PHC Group

2. Quality Management System

• Support the Management Representative in the company quality management system
• Maintain and update the document control system to ensure all quality-related documents are easily accessible, properly categorized, and up to date.
• Oversee the implementation and maintenance of Quality Management Systems (QMS) in accordance with ISO9001, GDPMDS and other relevant standards.
• Review and update ISO 9001 & GDPMDS documents when necessary and maintain records.
• Review and ensure all documents, including SOPs, work instructions, manuals, and forms, meet regulatory and company standards.
• Handle quality related matters such as non-conformances, customer complaints, change notification.
• Handle customer or supplier related enquiries, questionnaire and etc.
• Prepare for internal and external audits and ensure successful outcomes, tackle audit findings and recommendations in a timely manner
• Follow-up and verify corrective/preventive action (CAPA) effectiveness.
• Provide ISO 9001 and GDPMDS orientation to new employees

3. Compliance

• Coordinate, schedule and conduct required compliance orientation and training for employees
• Responsible to ensure compliance to regulations related to export controls and maintain records
• Provide support to employees on regulatory requirement and compliance procedures.
• Serve as a BizSafe member by overseeing and coordinating the preparation, management, and maintenance of all risk management and related documentation. Ensure all required documents are completed, up-to-date, and in compliance with BizSafe standards and regulations.

REQUIREMENTS

Candidates should bring with them

• A Degree in Life Sciences, Biomedical or any other related discipline.
• Minimum 2 years' experience in performing a similar job scope.
• Relevant experience in regulatory affairs will be advantageous
• Good knowledge and application of Microsoft 365.
• Able to work under a matrix reporting structure.
• Good organizational and time management skills.
• A strong database experience (Access, Excel) to set up functions, enter data or process information.
• Excellent interpersonal, presentation and verbal/written communications skills.
• Meticulous, able to work independently and timely in meeting deadlines.
• Integrity with a history of ethical decision-making is essential
• Sound knowledge of the regulatory requirements and legal framework for products and industry trends in the Asian Region.
• Knowledge in GDPMD, ISO9001, IVDR preferred.
• Familiarity with Health Science Authority's regulatory on medical devices, product registration, field safety correction and licensing requirements.

Welcome diversity and apply as you are!
At Adisseo, we cherish the value of diversity whatever it may be.

By joining Adisseo , you will join committed people who make the difference every day to contribute to this challenge.
By joining Adisseo , you will integrate a dynamic international environment.
By joining Adisseo , you will discover a world full of opportunities for every stage of your career by being actor to your professional journey.

Job Title : Regulatory Affairs Specialist

We are seeking a meticulous and proactiveRegulatory Affairs Specialist to ensure compliance with global regulatory requirements and support business operations. This role involves managing licenses and registrations, advising internal stakeholders, and staying ahead of regulatory changes. This role will work closely with the regional regulatory team and report functionally to Senior Regulatory Affairs Specialist. The ideal candidate will be highly organized, possess strong analytical skills, and thrive in both independent and collaborative work environments.

Key Responsibilities & Duties:

1. Regulatory Compliance & Monitoring

• Maintain and update a centralized regulatory database to track product licenses, renewal deadlines, and compliance documents.
• Monitor regulatory updates from local country teams and assess their impact on business operations.
• Implement a tracking system to ensure timely renewals, submissions, and compliance with evolving regulations.
• Ensure proper implementation of global processes (e.g., labelling, document requests) and contribute to continuous improvement.
• Support by working with cross-functions to respond to customer audit purposes and regulatory agency queries.

1. License & Registration Management

• Oversee end-to-end product registrations, including dossier preparation, submission, and follow-up with regulatory agencies.
• Renew licenses for existing products, ensuring adherence to labeling, MRL (Maximum Residue Limits), and safety requirements.
• Liaise with internal teams (R&D, Quality, Legal) and external stakeholders (regulatory bodies, third-party consultants) to resolve compliance issues.
• Prepare and submit regulatory dossiers for locally manufactured dilution products (Singapore-specific).
• Coordinate with Singapore authorities (e.g., SFA, NEA) to secure necessary approvals.

3. Documentation & System Maintenance

• Upload and maintain registration certificates, technical documents, and compliance records in the Product Lifecycle Management (PLM) system.
• Ensure data accuracy and completeness for audit readiness and regulatory inspections.
• Generate reports for management on registration statuses, expirations, and pending actions.
• Maintain records of formulation changes, batch records, and compliance certifications.

1. Stakeholder Communication & Business Support

• Advise HQ, sales, and supply chain teams on regulatory considerations for:
• New product launches (e.g., registration pathways, labeling compliance)
• Product amendments (e.g., formulation changes, claims adjustments)
• Sharing of related information from local teams (eg. updated requirements for import/export from local teams).
• Respond to customer regulatory requests, including undesirable substances declarations, safety data sheets (SDS), and supplier compliance questionnaires.
• Prepare customized compliance statements for clients based on regional regulatory requirements.
• Hold monthly alignment calls with country regulatory teams and senior regulatory affairs executive to track registration progress and address challenges.
• Support sales and supply chain teams by providing regulatory guidance for product distribution and market access.

Qualifications & Skills:

Education & Experience:

• Bachelor’s/Master’s degree in Regulatory Affairs, Chemistry, Life Sciences, or a related field.
• 2-3 years of experience in regulatory affairs, preferably in agrochemicals, pharmaceuticals, or consumer goods.
• Experience with APAC regulatory frameworks (e.g., China, India, ASEAN) is a plus.

Technical Skills:

• Proficiency in regulatory databases (e.g., PLM, SAP) and MS Office (Excel, PowerPoint).
• Knowledge of GLP, GMP, and ISO standards for compliance documentation.

Soft Skills:

• Strong attention to detail – Ensures accuracy in submissions and compliance records.
• Proactive problem-solving – Anticipates regulatory hurdles and proposes solutions.
• Excellent communication – Clearly conveys complex regulations to non-experts.
• Collaborative mindset – Works effectively with cross-functional teams.
• Results-driven – Committed to meeting KPIs (e.g., on-time renewals, audit pass rates).
• Service-oriented – Supports internal teams with a solutions-focused approach.
• Long-term thinker – Aligns regulatory strategies with business growth.

Alcotech Pte Ltd specializes in Infectious Disease Kits and Medical Device Regulatory Affairs. We support medical device manufacturers in navigating complex regulatory landscapes and securing market access across Singapore and Southeast Asia.

We are seeking a Regulatory Affairs Specialist with either experience working at the Health Sciences Authority (HSA) or prior experience in medical device regulatory affairs. The ideal candidate will manage medical device registrations, ensure compliance with regulations, and provide guidance on regulatory strategy.

• Prepare, review, and submit medical device registration dossiers to HSA. Monitor submissions in other ASEAN countries handled by local regulatory personnel.
• Advise on regulatory strategy, product classification, labeling, and compliance requirements.
• Monitor regulatory changes and provide guidance to ensure ongoing compliance in Singapore and ASEAN markets.
• Support post-market surveillance activities.
• Point of contact for manufacturers' regulatory team and regulatory authorities, ensuring smooth and timely registration processes.

• Minimum 2–5 years of regulatory affairs experience, either from prior work in HSA or a regulatory affairs role in medical devices.
• Strong knowledge of Singapore medical device regulations (HSA); familiarity with other ASEAN regulations is an advantage.
• Ability in speaking Chinese is a requirement.
• Strong organizational and project management skills; able to handle multiple submissions simultaneously.
• Familiarity with Therapeutic Products License (TPL) is preferred.

• Office-based role
• Monday – Friday, 9:00 am – 6:00 pm
• Location: 25 Bukit Batok Crescent, #09-13 The Elitist, Singapore 658066

$4,100 – $5,300 monthly, based on experience

• Leverage your HSA or regulatory affairs experience to lead submissions across multiple medical device product lines.
• Work closely with clients and regulatory authorities in a high-impact role.
• Gain exposure to ASEAN regulatory environments while building professional expertise.
• Join a specialist regulatory company offering career growth and professional development opportunities.

The Regulatory Affairs Executive in Pharmaceuticals based in New Delhi, India, will report to the Head of Regulatory Affairs / Managing Director. You will be responsible for managing the preparation and submission of regulatory documentation to health authorities to support the development, approval, and maintenance of pharmaceutical products. Your role will ensure compliance with national and international regulatory requirements throughout the product lifecycle.

Your key responsibilities will include:

• Approving labels, packaging, and promotional materials for compliance
• Summarizing scientific data
• Preparing regulatory dossiers for new product approvals, renewals, and variations
• Ensuring timely submissions to regulatory agencies
• Managing communication with health authorities
• Tracking regulatory changes
• Reviewing product materials for compliance
• Supporting clinical trials
• Maintaining regulatory databases
• Collaborating with cross-functional teams

To qualify, you should hold a Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related field, along with 4-5 years of experience in pharmaceutical regulatory affairs. Strong knowledge of global regulatory requirements from FDA, EMA, ICH, CDSCO, etc., attention to detail, critical thinking, organizational skills, and excellent communication skills are essential.

Preferred qualifications include Regulatory Affairs Certification (RAC) or equivalent, familiarity with global submission platforms, and experience in new drug applications and post-marketing surveillance.

This is a full-time position offering benefits such as cell phone reimbursement, day shift schedule, and a performance bonus. If qualified and interested in contributing to regulatory strategies during drug development and post-marketing phases, we encourage you to apply.

For inquiries, please contact Tanveer Kaur, HR, at +91 97hidden_mobile 3.

• Salary Range MYR 7,000 - 7,999
• City Bandar Sri Damansara
• Country Malaysia

• Identify regulatory requirements and stay up to date with the evolving regulatory landscape in each marketing territory.
  
• Serve as the company representative and committee member in local medical device industry associations (e.g., MMDA).
  
• Initiate, validate, review, plan, and strategize to ensure all products remain compliant with applicable statutory and regulatory requirements.
  
• Communicate regulatory updates to relevant internal stakeholders to ensure alignment across departments.
  
• Plan and drive process improvements, including the digitalization of Regulatory Affairs (RA) workflows.
  
• Oversee and maintain Medical Device Establishment/Dealer Licenses with the relevant authorities.
  
• Supervise pre-market regulatory activities including medical device registration, change notifications, and applications for special authorizations or exemptions with government bodies.
  
• Manage post-market regulatory obligations, including the reporting of device-related incidents and complaints, ensuring all submissions are timely and compliant with applicable requirements.
  
• Ensure compliance with advertisement and labeling regulations in each marketing territory.
  
• Oversee and supervise compliance with other regulatory requirements from authorities such as MOH (MY), HSA (SG), NEA (SG), IMDA (MY/SG), DVS (MY/SG), and AVS (MY/SG).
  
• Plan and lead the implementation of internal RA audits on an annual basis.
  
• Support external audits conducted by regulatory agencies, principals, and suppliers by providing regulatory input to minimize the risk of non-compliance findings.
  
• Provide regulatory support during internal audits of subsidiaries and associated companies across Southeast Asia.
  
• Collaborate with Conformity Assessment Bodies on product risk assessment and regulatory implementation changes.
  
• Support regulatory matters related to custom import requirements and documentation.
  
• Assist and oversee matters involving licensed pharmacists or qualified personnel, including Poison A License and inspections by the Ministry of Health.
  

• Possess a Bachelor’s Degree in Science or a related discipline, with a minimum of 7 years of relevant experience in a similar capacity.
  
• Proficient in Microsoft Office applications, including Outlook, Excel, Word, and PowerPoint.
  
• Demonstrated track record in team leadership, preferably with experience managing a team of five or more, with strong people management capabilities including coaching and training.
  
• Excellent communication and interpersonal skills, with the ability to engage with regulatory authorities, consultants, auditors, and foreign manufacturers,effectively.
  
• In-depth knowledge and hands-on experience in medical device registration and regulatory compliance, particularly in Malaysia, Singapore, and Indonesia.
  
• Solid understanding of quality management systems, specifically ISO 13485, ISO 9001, and GDPMD requirements.
  
• Basic biomedical knowledge with the ability to understand and interpret technical aspects of medical devices.
  
• Strong understanding of operational workflows, with the ability to identify inefficiencies and implement process improvements.
  
• Meticulous and detail-oriented, capable of working independently with minimal supervision.
  
• Possess strong analytical and presentation skills, with the ability to translate data into meaningful insights.
  
• Proactive, performance-driven, and results-oriented, with a strong sense of ethical integrity and accountability in project execution.
  
• Pharmacist background with a valid license will be an added advantage.