24 Regulatory Affairs Executive Jobs - June 2026 - Urgent Hiring
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"regulatory affairs executive"
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Regulatory Affairs & Product Development Executive
MYR4,000 - MYR5,000 Sebulan
Bandar Kuala Lumpur, WP Kuala Lumpur
Dekat Stesen Tren
Syarikat ini berdekatan dengan stesen tren
- Support product registration and regulatory submissions across multiple international markets
- Liaise with suppliers, manufacturers and regulatory authorities on product compliance matters
- Prepare and maintain product documentation, regulatory dossiers and compliance records ...
Regulatory Affairs
Product Development
Kemahiran Diperlukan
Regulatory Affairs
Product Development
Compliance
Quality Assurance
Project Management
Market Analysis
+4
Posted
3 days ago
SGD3,200 - SGD3,200 Sebulan
Singapore
- Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.
- Liaise with local authorities to provide relevant legislation and compliance requirement so as to advise suppliers and internal stakeholders.
- Provide guidelines for the required documents to the supplier management team for new product screening. ...
Posted
a month ago
Undisclosed
- Review and approve product labels to ensure compliance with local and export regulatory requirements.
- Provide accurate regulatory and statutory information for inclusion in product packaging and artwork.
- Review product formulations to ensure ingredients and food additives comply with local and export market regulations. ...
Posted
25 days ago
Undisclosed
- Handle medical device product registrations, renewals, and change notifications with the Medical Device Authority (MDA).
- Apply for, maintain, and renew the company's Establishment Licence and other regulatory approvals.
- Prepare and submit regulatory applications and follow up closely on authority queries through to approval. ...
Posted
9 days ago
MYR3,000 - MYR3,982 Sebulan
- Handle medical device product registrations, renewals, and change notifications with the Medical Device Authority (MDA).
- Apply for, maintain, and renew the company's Establishment Licence and other regulatory approvals.
- Prepare and submit regulatory applications and follow up closely on authority queries through to approval. ...
Posted
8 days ago
Undisclosed
- Support local regulatory work, including new product/devices/cosmetic products registration, variations and renewals
- Co-ordination of regulatory related submission/correspondence with respective local health authorities (including National Pharmaceutical Regulatory Agency, NPRA, Pharmacy Enforcement Divison and Medical Device Authority, MDA)
- Maintenance of regulatory related database and licences such as product technical files maintenance, product complaint & adverse drug reactions (ADRs) records, import and poison A licences, etc ...
Posted
2 days ago
Undisclosed
Petaling
- Manage food safety & halal certification processes, ensuring compliance in a timely manner.
- Manage and maintain food safety certification systems such as HACCP, GMP, Mesti, Halal, keeping records current and fully compliant.
- Act as the primary liaison with the relevant certification bodies, auditors, and stakeholders to resolve compliance queries and facilitate audits. ...
Posted
10 days ago
Menarini Asia-Pacific
Undisclosed
Singapore
- Regional Lead in new registration submissions and life cycle management projects of medical devices and cosmetics in APAC regions. Examples for life cycle projects include technical variations (such as change in manufacturer, formulation change, etc).
- Regional Lead in regulatory-status re-classification projects to serve commercial marketing needs.
- Timely management and execution of registration activities for assigned product portfolios, responsible to monitor and provide update of project progress to completion to stakeholders. ...
Posted
8 days ago
Undisclosed
Singapore
- 2-3 years of regional regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
2 days ago
SGD4,500 - SGD4,500 Sebulan
Singapore
- 3 years of regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
7 days ago
Undisclosed
Singapore
- 2-3 years of regional regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
8 days ago
SGD4,500 - SGD4,500 Sebulan
Singapore
- 3 years of regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
23 days ago
Undisclosed
Singapore
- 2-3 years of regional regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
24 days ago
SGD4,500 - SGD4,500 Sebulan
Singapore
- 3 years of regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
a month ago
Undisclosed
Singapore
- 2-3 years of regional regulatory affairs experience in the Pharmaceutical industry
- Experience with regulatory submissions (registrations, post-approval variations)
- Related science degree ...
Posted
a month ago
SGD1,000 - SGD2,000 Sebulan
Singapore
- To Coordination of product registration (new and renewal) in the designated countries including provision of documents for dossier preparation and certificates within the specified timeframe proactively to complete product registration.
- Point of contact between factories and the regulatory team of designated countries.
- To Provide regulatory assessment for new product/change introduction ...
Posted
5 days ago
SIREHEMAS PHARMA SDN BHD
MYR2,500 - MYR3,500 Sebulan
- Manage product registration and regulatory submissions for pharmaceutical, supplement, food supplement, and medical device products.
- Handle NOT (Notification of Cosmetic Products) registration independently.
- Manage and coordinate overseas product registration, especially with foreign regulatory authorities such as BPOM (Indonesia). ...
Posted
8 days ago
SGD1,000 - SGD2,000 Sebulan
Singapore
- To Coordination of product registration (new and renewal) in the designated countries including provision of documents for dossier preparation and certificates within the specified timeframe proactively to complete product registration.
- Point of contact between factories and the regulatory team of designated countries.
- To Provide regulatory assessment for new product/change introduction ...
Posted
18 days ago
DCH Auriga (Malaysia) Sdn Bhd
Undisclosed
- Manage pre-market and post-market regulatory activities, including product registration, licence renewals, import permits, special authorisations, product recalls, and lifecycle updates.
- Act as Deputy Pharmacovigilance (PV) Officer, overseeing PV-related functions such as regulatory reporting, audit participation, training, and closure of audit findings.
- Conduct local literature monitoring to support pharmacovigilance requirements. ...
Posted
19 hours ago
Executive, Network Scheduling - Regulatory Affairs Executive, Network Scheduling - Regulatory Affairs
Malaysia Aviation Group
Undisclosed
KL City
- To coordinate, submit, and secure timely all the landing permits, overflight permits, and regulatory approvals for scheduled, charter, cargo, ferry, ad hoc, and special flight operations for Malaysia Airlines, Firefly, MASKargo, and AMAL in accordance with operational and regulatory timelines.
- To assist and support FAOC applications for renewals, amendments, and variation approvals for new destinations, routes, aircraft types, and operational, changes, ensuring continuous operational eligibility in all applicable countries.
- To monitor and ensure all the flight approvals, permits, clearances, and regulatory requirements are obtained in a timely manner and remain valid prior to flight operations, including the tracking approval validity, expiry dates, permit conditions, and operational restrictions imposed by the authorities. Proactively following up with authorities, agents and station heads to prevent operational delays and disruptions that could impact flight schedules and commercial commitments. ...
Posted
6 days ago
Undisclosed
KL City
- To coordinate, submit, and secure timely all the landing permits, overflight permits, and regulatory approvals for scheduled, charter, cargo, ferry, ad hoc, and special flight operations for Malaysia Airlines, Firefly, MASKargo, and AMAL in accordance with operational and regulatory timelines.
- To assist and support FAOC applications for renewals, amendments, and variation approvals for new destinations, routes, aircraft types, and operational, changes, ensuring continuous operational eligibility in all applicable countries.
- To monitor and ensure all the flight approvals, permits, clearances, and regulatory requirements are obtained in a timely manner and remain valid prior to flight operations, including the tracking approval validity, expiry dates, permit conditions, and operational restrictions imposed by the authorities. Proactively following up with authorities, agents and station heads to prevent operational delays and disruptions that could impact flight schedules and commercial commitments. ...
Posted
7 days ago
Undisclosed
Petaling
- Act as the key liaison between the organization and government agencies, ministries, regulators, and local authorities to support effective stakeholder engagement.
- Build and maintain strong professional relationships with government officials and stakeholders, including coordinating meetings, briefings, and site visits.
- Monitor, interpret, and provide updates on relevant laws, regulations, and government policies that may impact the organization. ...
Posted
23 days ago
MYR4,500 - MYR6,000 Sebulan
- Degree in a relevant scientific or technical field (e.g., Pharmacy, Life Sciences).
- At least 5 years working experience in Construction of cleanroom and/or related field is an advantage.
- Excellent communication, analytical, problem-solving, and organizational skills; ability to manage multiple projects. ...
Posted
a day ago
Undisclosed
Singapore
- Prepare and submit regulatory dossiers for product registrations, change notifications, and renewals for designated SEAT countries based on ASEAN CSDT format. Monitor regulatory submission status and maintain accurate, up-to-date RA/QA records and databases.
- Review product labelling and promotional materials to ensure compliance with local regulatory requirements.
- Conduct regulatory intelligence and communicate local regulatory requirements and updates to relevant stakeholders. ...
Posted
19 days ago
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