200+ Regulatory Affairs Jobs - September 2026 - High Salaries

Showing 229 jobs results for "regulatory affairs"
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Undisclosed

Hong Kong

Posted
17 days ago
Undisclosed

Hong Kong

Posted
17 days ago
Undisclosed

台灣

Posted
10 days ago
Undisclosed

Hong Kong

Posted
17 days ago
SGD4,000 - SGD4,000 Per Month

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
18 days ago
MYR2,500 - MYR3,000 Per Month
  • To do checking and amendment on product information, labels, artwork and other documents as required for the regulatory compliance.
  • Ensure local and international market regulatory requirements are in compliance.
  • To apply for documents which need for export use such as Certificate of Pharmaceutical Product (CPP) and Certificate of Free Sale (CFS). ...
Posted
10 days ago
MYR2,500 - MYR3,000 Per Month

Lahat

  • To do checking and amendment on product information, labels, artwork and other documents as required for the regulatory compliance.
  • Ensure local and international market regulatory requirements are in compliance.
  • To apply for documents which need for export use such as Certificate of Pharmaceutical Product (CPP) and Certificate of Free Sale (CFS). ...
Posted
18 days ago
Undisclosed

台灣

Posted
18 days ago
MYR2,500 - MYR3,000 Per Month

Lahat

  • To do checking and amendment on product information, labels, artwork and other documents as required for the regulatory compliance.
  • Ensure local and international market regulatory requirements are in compliance.
  • To apply for documents which need for export use such as Certificate of Pharmaceutical Product (CPP) and Certificate of Free Sale (CFS). ...
Posted
18 days ago
Undisclosed

Singapore

  • Anticipate regulatory risks and proactively develop mitigation plans.
  • Serve as the RA project lead, coordinating with cross-functional teams (e.g., Medical, QA, Supply Chain, Commercial, BD) to drive project execution.
  • Lead cross-functional team (CFT) discussions to ensure alignment on regulatory strategy, timelines, and deliverables. ...
Posted
23 days ago
MYR2,500 - MYR3,000 Per Month

Lahat

  • To do checking and amendment on product information, labels, artwork and other documents as required for the regulatory compliance.
  • Ensure local and international market regulatory requirements are in compliance.
  • To apply for documents which need for export use such as Certificate of Pharmaceutical Product (CPP) and Certificate of Free Sale (CFS). ...
Posted
18 days ago
Undisclosed

Singapore

  • Anticipate regulatory risks, identify opportunities, and implement mitigation plans.
  • Align local priorities with regional and global regulatory strategies.
  • Health Authority & External Engagement ...
Posted
18 days ago
Undisclosed

Bandar Baru Klang

  • Assist in applications and renewals of licences, permits and certificates.
  • Liaise with MDA, suppliers, manufacturers and internal departments on regulatory matters.
  • Review product documents such as certificates, technical documents, labelling, IFU and declarations of conformity. ...
Posted
23 days ago
Undisclosed

Singapore

  • Prepare & submit product registration documentation & other relevant licences’ application and ensure submissions are complete, properly formatted, and comply with applicable regulatory requirements that lead to timely approval of new product registration in Singapore
  • Notify and update Health Sciences Authority (HSA) of any change of particulars / documents related to product registration
  • Ensure changes to the approved products and other relevant licenses are timely submitted to authorities as required ...
Posted
24 days ago
MYR2,500 - MYR3,500 Per Month
  • Opportunities for promotion
  • Responsibilities:
  • To register traditional, heath supplement, OTC products. ...
Posted
25 days ago
Undisclosed
  • Provide regulatory support for product launches and lifecycle management activities.
  • Monitor regulatory changes and assess their impact on the business.
  • Collaborate with Commercial, Quality, Pharmacovigilance, Supply Chain, and Technical teams to ensure compliance and business continuity. ...
Posted
a day ago
Undisclosed

Singapore

  • Engaging directly with regulatory authorities
  • Monitoring regulatory changes and developing appropriate strategies
  • Advising internal stakeholders on regulatory requirements ...
Posted
25 days ago
Undisclosed

KL City

  • Assist with client documentation review, gap analysis, provide input regarding the acceptability of existing data, and explain how to satisfy the submission requirements.
  • Assist with or redirect internal or external inquiries related to quoting project hours and scope, including potential grouping or classification as applicable.
  • Escalate complex regulatory issues identified by team or clients to senior experts as appropriate and follow through to resolution. ...
Posted
21 days ago
Undisclosed

Singapore

  • Anticipate regulatory risks, identify opportunities, and implement mitigation plans.
  • Align local priorities with regional and global regulatory strategies.
  • Health Authority & External Engagement ...
Posted
21 days ago
Undisclosed

Singapore

  • Develops and coordinates APAC regulatory strategies and regulatory plans.
  • Working with department management, communicates with international regulatory authorities.
  • Coordinates/prepare and maintains regulatory submissions according to country registration requirements to facilitate product approvals in APAC. ...
Posted
21 days ago
Undisclosed

Hong Kong

  • Liaising with stakeholders internally to generally educate, train, support and assist as to licensing, regulatory and compliance issues, queries, consultations, etc
  • Maintaining a relationship with external parties, in particular OFCA, including:
  • Responding to filing requirements, complaints, inquiries, consultations, etc on regulatory and compliance matters ...
Posted
8 days ago
Undisclosed
  • Receive, process, assess and report adverse events, product complaints and other safety information in accordance with local and global regulatory requirements.
  • Ensure Individual Case Safety Reports (ICSRs) are complete, accurate and submitted within regulatory timelines.
  • Perform follow-up activities to obtain complete and medically relevant safety information. ...
Posted
a month ago
Undisclosed
  • Work closely with internal and external stakeholders (i.e. Pharmacovigilance, Marketing, Quality Assurance, Finance, Regulatory Authorities) to ensure all the responsibilities and agreed services for the clients are met.
  • Understand and adhere to company’s regulatory affairs SOP
  • Full understanding on the business models and key processes related to Zuellig Pharma’s operations and structure that will affect services and responsibilities ...
Posted
a month ago
MYR2,000 - MYR3,000 Per Month
  • Keep abreast of University policies, procedures and developments in internal auditing, and perform other audit-related duties as assigned.
  • Assist the Head in implementing quality assurance activities and ensuring compliance with University policies, MQA, JPT and other regulatory requirements.
  • Support the preparation and submission of documentation for programme accreditation, renewal, approval, changes and other regulatory requirements, including MQA and JPT applications. ...
Posted
9 days ago
Undisclosed
  • Work closely with internal and external stakeholders (i.e. Pharmacovigilance, Marketing, Quality Assurance, Finance, Regulatory Authorities) to ensure all the responsibilities and agreed services for the clients are met.
  • Understand and adhere to company’s regulatory affairs SOP
  • Full understanding on the business models and key processes related to Zuellig Pharma’s operations and structure that will affect services and responsibilities ...
Posted
22 days ago
Undisclosed

台灣

Posted
18 days ago
Undisclosed

KL City

  • Own the preparation of all regulatory submissions, including:
  • Technical File / Design Dossier
  • FDA pre-subs, 510(k), or De Novo packages ...
Posted
18 days ago