200+ Regulatory Affairs Jobs - July 2026 - High Salaries
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"regulatory affairs"
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SIREHEMAS PHARMA SDN BHD
MYR2,500 - MYR3,500 Per Month
- Prepare, submit, and maintain regulatory dossiers in compliance with local and overseas regulatory requirements.
- Handle product variations, renewals, and post-market regulatory obligations.
- Liaise directly with regulatory authorities for technical queries, clarifications, audits, and inspections. ...
Posted
24 days ago
Menarini Asia-Pacific
Undisclosed
Singapore
- Work closely with manufacturers and country regulatory teams for prompt response to submission queries, ability to analyze and identify gaps to address Authority needs.
- Review and approve artwork for Asia Pacific with base knowledge of labelling requirements in individual countries according to in-house artwork system, ability to address and resolve labeling issues when required.
- Maintain medical device dealer licenses and class A licenses (Singapore) on behalf of regional office and support cross-border E-commerce registration initiatives. ...
Posted
24 days ago
RECRUITPEDIA PTE. LTD.
SGD5,000 - SGD5,000 Per Month
Singapore
- Monitor regulatory changes, assess impact, and advise stakeholders on compliance requirements
- Maintain product registration database and track submission status, approvals, and renewals
- Support regulatory compliance across the full product lifecycle (development to post-market) ...
Posted
a month ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities
- Maintain and update regulatory databases and ensure documentation accuracy and compliance
- Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements ...
Posted
2 days ago
Undisclosed
Singapore
- Assess and review scientific and technical data provided by subject matter experts for regulatory submissions, ensuring alignment with JAPAC and regional requirements, identifying gaps, and developing mitigation strategies as needed.
- Effectively present regulatory data to RA affiliates and ensure complete and timely responses to authorities for Clinical trial applications, New Drug/ New indication applications and any other assigned applications.
- Collaborate cross-functionally with Commercial, Medical Affairs, Market Access, Clinical Development, and CMC teams, represent the regulatory function and provide strategic input to enable product registrations, mitigate regulatory risks, and ensure compliance. ...
Posted
14 days ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities
- Maintain and update regulatory databases and ensure documentation accuracy and compliance
- Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements ...
Posted
6 days ago
Undisclosed
KL City
- Guiding affiliates in pursuing accelerated regulatory pathways (reliance, fast track, abridged) and supporting risk and issue management with health authorities
- Provide strategic and tactical regulatory input to develop the portfolio LCM plan to enable supply mitigations and/or optimizations.
- Help map and elevate regulatory advocacy capabilities & strategies across southeast Asia ...
Posted
a month ago
Essex Bio-Technology
Undisclosed
Singapore
- Manage new and existing supplier management activities.
- Manage investigations for deviation, non-conformity, CAPA and complaints.
- Review technical documentation and perform basic investigation. ...
Posted
a month ago
SGD4,500 - SGD4,500 Per Month
Singapore
- Candidates with adequate Regional experience will be considered for a Senior Specialist position
- An excellent opportunity has come up with an international Pharmaceutical MNC and they are currently looking for a Senior Regional Regulatory Affairs Executive to join the team in Singapore.
- The successful incumbent will drive the implementation of global guidelines and work alongside local RA functions to ensure product approvals. You will also exhibit strong interpersonal skills and work closely with cross-functional departments to support the formulation of long-term regulatory strategy. ...
Posted
15 days ago
Undisclosed
KL City
- Guiding affiliates in pursuing accelerated regulatory pathways (reliance, fast track, abridged) and supporting risk and issue management with health authorities
- Provide strategic and tactical regulatory input to develop the portfolio LCM plan to enable supply mitigations and/or optimizations.
- Help map and elevate regulatory advocacy capabilities & strategies across southeast Asia ...
Posted
a month ago
Undisclosed
Hong Kong
- Regulatory Affairs support
- Support the registration of NCE and change of particulars in Hong Kong
- Review the packaging of products to ensure the compliance with Laws and Regulations in Hong Kong ...
Posted
25 days ago
Undisclosed
Eastern Distr.
- Maintain all regulatory related documents
- Support HK tendering documents
- Oversee third-party repacking/redressing and product release ...
Posted
a month ago
Regulatory Affairs Specialist (Contract-Up to $5500) Regulatory Affairs Specialist (Contract-Up to $5500)
PERSOL SINGAPORE PTE. LTD.
SGD4,000 - SGD4,000 Per Month
Singapore
- Assist with assigned rebranding activities for SEA team.
- Assist with pre-market regulatory clearances and post-market regulatory activities.
- Familiarize with registration requirement. ...
Posted
24 days ago
EPIC MEDICAL PTE. LTD.
SGD4,500 - SGD5,000 Per Month
Singapore
- Execute pre-market activities required to support the entire lifecycle of a medical device
- Involve in product design verification and validation activities according to regulatory requirements
- Establish technical files and 510k documentation to support CE marking and FDA clearance for Class I and II medical devices ...
Posted
a month ago
Undisclosed
Singapore
- An excellent opportunity has come up with an international Pharmaceutical MNC and they are currently looking for a Senior Regional Regulatory Affairs Executive to join the team in Singapore.
- The successful incumbent will drive the implementation of global guidelines and work alongside local RA functions to ensure product approvals. You will also exhibit strong interpersonal skills and work closely with cross-functional departments to support the formulation of long-term regulatory strategy.
- REQUIREMENTS ...
Posted
18 days ago
Undisclosed
Hong Kong
- Research and interpret regulations related to IVDs and medical devices, tracking updates to regulations, guidelines and standards, and communicating promptly with the manufacturer for the impact and updates.
- Responsible for post-market surveillance of listed IVDs and medical devices based on related regulations and company SOPs.
- Ensure quality documentation meets both company standards and Hong Kong regulatory requirements. ...
Posted
23 days ago
Undisclosed
- Highly competent with systems (e.g. PLM)
- Background in food regulatory affairs
- Minimum years of experience required: 3-5 years ...
Posted
25 days ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities
- Maintain and update regulatory databases and ensure documentation accuracy and compliance
- Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements ...
Posted
7 days ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities
- Maintain and update regulatory databases and ensure documentation accuracy and compliance
- Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements ...
Posted
8 days ago
Senior Specialist, Commercial Quality - Regulatory Affairs Senior Specialist, Commercial Quality - Regulatory Affairs
Beckman Coulter Diagnostics
Undisclosed
Singapore
- Bachelor’s degree with 6+ years of relevant experience or a certificate in medical devices with 3 years of experience or 4+ years of experience in the medical devices or a related industry.
- Understands Regulatory Affairs concepts and is should be familiar with regulations/ guidelines governing development of diagnostic products
- Ability to prioritize, multitask, and organize work, succeed in a fast-paced environment with capability to be flexible and adaptable to meet business needs ...
Posted
a month ago
Undisclosed
KL City
- Leads supply optimization discussions (stock build/stock depletion/registration deletion/commercialization of validation batches).
- Sets up priorities, organizes, oversees and monitors activities, towards division’s and country's objectives achievement in compliance with policies and standards.
- Lead and coordinates E2E regulatory process for supply chain changes as per guidelines for the APJ (inc China) region as well as regulatory requirements from other regions globally ...
Posted
23 days ago
Undisclosed
Singapore
- Leads supply optimization discussions (stock build/stock depletion/registration deletion/commercialization of validation batches).
- Sets up priorities, organizes, oversees and monitors activities, towards division’s and country's objectives achievement in compliance with policies and standards.
- Lead and coordinates E2E regulatory process for supply chain changes as per guidelines for the APJ (inc China) region as well as regulatory requirements from other regions globally ...
Posted
23 days ago
Undisclosed
Hong Kong
- Closely collaborate with regional regulatory expertise in the Therapeutic Areas in both labelling and CMC aspects.
- Design, deploy and maintain processes and/ or systems to manage external stakeholders, of which includes local change implementation management. External stakeholders include, but not limited to, provision of documents and liaison with local third party, government tendering bodies, Hospital Authority, etc.
- Provide regulatory support, including oversight of product launch and implementation timelines to internal and external stakeholder. ...
Posted
a month ago
SGD4,000 - SGD4,000 Per Month
Singapore
- Submit license renewals timely.
- Assess impact of changes initiated by Product Owner and work closely with the supply chain, manufacturing and commercial teams to ensure no disruption to supply.
- Provide internal stakeholders with regular updates throughout the registration process. ...
Posted
7 days ago
Senior Specialist, Commercial Quality - Regulatory Affairs Senior Specialist, Commercial Quality - Regulatory Affairs
Beckman Coulter Diagnostics
Undisclosed
Singapore
- Bachelor’s degree with 6+ years of relevant experience or a certificate in medical devices with 3 years of experience or 4+ years of experience in the medical devices or a related industry.
- Understands Regulatory Affairs concepts and is should be familiar with regulations/ guidelines governing development of diagnostic products
- Ability to prioritize, multitask, and organize work, succeed in a fast-paced environment with capability to be flexible and adaptable to meet business needs ...
Posted
a month ago
SGD5,500 - SGD5,500 Per Month
Singapore
- Liaise with internal teams and external stakeholders to resolve regulatory queries and support product registration activities
- Maintain and update regulatory databases and ensure documentation accuracy and compliance
- Develop and maintain SOPs and internal regulatory policies to ensure compliance with regulatory requirements ...
Posted
15 days ago
SGD4,500 - SGD4,500 Per Month
Singapore
- Candidates with adequate Regional experience will be considered for a Senior Specialist position
- An excellent opportunity has come up with an international Pharmaceutical MNC and they are currently looking for a Senior Regional Regulatory Affairs Specialist to join the team in Singapore.
- The successful incumbent will drive the implementation of global guidelines and work alongside local RA functions to ensure product approvals. You will also exhibit strong interpersonal skills and work closely with cross-functional departments to support the formulation of long-term regulatory strategy. ...
Posted
23 days ago
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