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100+ Regulatory Affairs Jobs - August 2026 - Urgent Hiring
Showing 176 jobs results for
"regulatory affairs"
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Manage Alert
Undisclosed
Singapore
- Established Japanese Medical Devices MNC
- New headcount with regional scope across Asia
- Base salary up to $7,500/month + AWS + VB ...
Posted
18 days ago
Senior Specialist, Commercial Quality - Regulatory Affairs Senior Specialist, Commercial Quality - Regulatory Affairs
Beckman Coulter Diagnostics
Undisclosed
Singapore
- Lead pre-market and post-market regulatory activities for IVD devices, including preparation and submission of technical documentation, regulatory applications, change notifications, renewals, and responses to regulatory bodies and partners.
- Maintain and manage regulatory intelligence and compliance at local, regional, and global levels, ensuring adherence to applicable regulations throughout the product lifecycle.
- Oversee quality management processes and continuous improvement, including compliance operations, audits, CAPA, distributor and warehouse oversight, and acting as Quality Management Representative (QMR) when required. ...
Posted
25 days ago
Undisclosed
Singapore
- Lead US IND strategy with direct FDA engagement
- High-impact role ahead of global trial in 2027
- Lead the design and execution of global regulatory strategies across pipeline assets ...
Posted
a month ago
Undisclosed
Singapore
- Established Japanese Medical Devices MNC
- New leadership role for newly established Regional HQ in Singapore
- Base salary from $10,000 - $15,000/month ...
Posted
22 days ago
SGD15,000 - SGD15,000 Per Month
Singapore
- Lead and provide strategic direction to the Financial Reporting & Standards and Inspection functions.
- Drive capability development by strengthening technical expertise, leadership competencies, and succession planning across the division.
- Lead transformation initiatives across the audit and accounting regulatory areas by driving process improvements, adoption of AI and data-enabled approaches to strengthen regulatory effectiveness, enhance operational efficiency and support the sector’s continued development. ...
Posted
22 days ago
Undisclosed
Singapore
- Own APAC regulatory strategy and ensure compliance across relevant sectors (food & nutrition plus select non-food categories).
- Enable commercialization: guide claims, labels, and marketing communications with science-based, compliant positions.
- Lead approvals/registrations where required to support market access across APAC. ...
Posted
25 days ago
Undisclosed
- Drive Product Registration, re-registration, change notification and related license applications & maintenance.
- Drive product lifecycle management activities (labeling changes, new regulations assessment and preparation, CPDS, promotional material reviews)
- Manage administrative and coordination activities e.g., project & metric management, archival of licenses/ permit, invoice & payment tracking and follow up, operational support etc. ...
Posted
a month ago
Undisclosed
KL City
- Develop regulatory strategies and submission plans of new products, including expansion of existing product portfolio into new territories (ensure timely and smooth product launches according to marketing plans).
- Act as an advisor to company management on regulatory and legislative requirements of new territories and if necessary, to manage third-party regulatory service providers to ensure services rendered are as agreed according to existing agreements in place.
- Keep abreast with new or changing regulations and coordinate with internal and external stakeholders to develop strategies to address changes in product/ operations/ testing requirements, while ensuring minimal or no disruption to stock supply. ...
Posted
a month ago
Undisclosed
Singapore
- Bachelor's Degree in Engineering, Bioengineering/Biomedical, Science, or related field with 6 years of relevant working experience in healthcare innovation
- Industry experience in regulatory submission with familiarity in ISO 13485, ISO 14971, IEC 62304, IEC 60601, and ISO 27001 and Health Sciences Authority (HSA) regulatory submissions
- Experience with medical device and Software as Medical Device (SaMD) regulatory requirements and maintenance plans ...
Posted
a month ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Determine whether products are classified as medical devices and identify appropriate regulatory pathways and risk classifications
- Prepare and submit regulatory applications including product registrations, renewals, and change notifications to relevant authorities
- Follow up on submissions and address authority feedback to support successful approvals ...
Posted
18 days ago
Undisclosed
Singapore
- Lead as the primary RA resource within SC project teams.
- Drive the regulatory assessment and documentation of manufacturing changes and distribution requirements, ensuring global regulatory compliance (e.g. US FDA, EU MDR, TGA, Health Canada, ANVISA, …).
- Collaborate with cross-functional teams such as quality, manufacturing, engineering, SC, and RA leads to gather input, align on regulatory requirements and resolve queries related to device changes, manufacturing transfers/issues or SC transformation projects. ...
Posted
a month ago
SGD2,000 - SGD2,000 Per Month
Singapore
- Prepare, compile, and coordinate the submission of regulatory dossiers for medical device registrations in compliance with applicable regulatory requirements.
- Coordinate with regulatory authorities and internal and external stakeholders to facilitate regulatory activities, support product registrations, and address regulatory queries.
- Monitor regulatory submissions and maintain regulatory status records to ensure timely approvals and compliance with regulatory timelines. ...
Posted
22 days ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Determine whether products are classified as medical devices and identify appropriate regulatory pathways and risk classifications
- Prepare and submit regulatory applications including product registrations, renewals, and change notifications to relevant authorities
- Follow up on submissions and address authority feedback to support successful approvals ...
Posted
20 days ago
Undisclosed
Singapore
- Bachelor’s Degree preferably in Life Sciences, Engineering, Computer Science or Business with 10 years of relevant working experience in healthcare innovation
- Industry experience in regulatory submissions with familiarity in ISO 13485, ISO 14971, IEC 62304, IEC 60601, and ISO 27001 standards and Health Sciences Authority (HSA) regulatory submissions
- Proven track record in regulatory registration of medical devices and medical-use software and managing international certification projects and engaging with health authorities ...
Posted
a month ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Determine whether products are classified as medical devices and identify appropriate regulatory pathways and risk classifications
- Prepare and submit regulatory applications including product registrations, renewals, and change notifications to relevant authorities
- Follow up on submissions and address authority feedback to support successful approvals ...
Posted
22 days ago
SGD4,000 - SGD4,000 Per Month
Singapore
- Manage end-to-end regulatory registration activities, including product testing, clinical evaluations, quality system assessments, and submissions for multi-country market access.
- Prepare and submit regulatory filings for Singapore and other markets.
- Communicate with regulatory authorities and monitor submission timelines to ensure timely approvals. ...
Posted
16 days ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Determine whether products are classified as medical devices and identify appropriate regulatory pathways and risk classifications
- Prepare and submit regulatory applications including product registrations, renewals, and change notifications to relevant authorities
- Follow up on submissions and address authority feedback to support successful approvals ...
Posted
a month ago
UMediC Group Berhad
Undisclosed
Malaysia
- Strong skills in Regulatory Documentation and Regulatory Submissions, with experience preparing, reviewing, and compiling technical files and registration dossiers.
- Sound understanding of Regulatory Compliance and Regulatory Requirements, including relevant medical device regulations, standards, and guidelines.
- Practical experience in Regulatory Affairs, including interactions with regulatory authorities, certification bodies, and internal stakeholders. ...
Posted
2 days ago
Undisclosed
KL City
- Government Relations & Stakeholder Management
- Build and nurture strategic relationships with regulators, government agencies, and relevant industry associations.
- Initiate early engagement with regulators to understand upcoming regulations, influence policy direction where appropriate, and prepare internal teams for potential impacts. ...
Posted
a month ago
SGD2,200 - SGD2,800 Per Month
Pasir Ris
- Coordinate the collection, compilation, and formatting of tender documents to support timely submissions
- Manage and maintain tender schedules and monitor submission deadlines to ensure on-time completion
- Liaise with internal departments to obtain required documents and information for tender submissions ...
Posted
a day ago
Undisclosed
KL City
- Minimum 5 years of in-depth and hands-on regulatory submission experience in the medical device industry.
- Proven collaboration with global counterparts for ensuring efficiency and collaboration in RAQA inititiatives.
- Ability to operate in a business-driven model providing quick, salient analysis and concrete action plans emphasis on understanding and anticipating business needs and interests and devising proactive approaches/responses. ...
Posted
a day ago
Undisclosed
Singapore
- Quality Oversight & Compliance
- Batch Review & Product Release
- Investigations & Change Management ...
Posted
5 days ago
Undisclosed
KL City
- Job Purpose:
- To provide compliance advisory in projects and new business assessment, manage regulatory breaches and regulatory relationship, disseminate new/revised regulations to stakeholders, review Gap Analysis conducted by stakeholders to ensure compliance to the regulatory requirements through close liaison with stakeholders.
- Key Responsibilities: ...
Posted
6 days ago
Undisclosed
Singapore
- Evaluate the Chemistry, Manufacturing and Controls (CMC) data of therapeutic product applications for regulatory approval to assure the quality of medicines supplied in Singapore.
- Provide advice / guidance on the regulatory requirements and procedures for therapeutic product regulatory submissions, and to respond to enquiries from industry and healthcare stakeholders as well as member of public.
- Participate in projects and process/regulatory review. ...
Posted
7 days ago
Undisclosed
Singapore
- at least 10 years experience within the financial services industry, with a focus on regulatory compliance, risk management or control frameworks
- Strong understanding of the Singapore regulatory environment, with awareness of broader APAC developments
- Experience in regulatory engagement, including dealing with regulatory enquiries or incidents ...
Posted
8 days ago
Undisclosed
WFH
Singapore
- Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials;
- Prepare, review, and submit to Regulatory Agencies;
- Communicate with global study teams and personnel on study progress; ...
Posted
8 days ago
Undisclosed
Singapore
- Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials;
- Prepare, review, and submit to Regulatory Agencies;
- Communicate with global study teams and personnel on study progress; ...
Posted
9 days ago
Undisclosed
Singapore
- Evaluate AI-generated artifacts against domain-specific quality rubrics.
- Identify factual, aesthetic, and presentation errors.
- Provide clear, structured written feedback. ...
Posted
13 days ago
Undisclosed
Singapore
- Regulations
- Communications & Engagement
- Workforce & Strategic Partnerships ...
Posted
18 days ago
Undisclosed
KL City
- Responsible for supporting the execution of various Traded Goods and Raw Material requests in an efficient and timely manner.
- Manage specification approvals for all raw materials.
- Conducts administrative duties within defined guidelines. ...
Posted
18 days ago
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