Senior Regulatory Strategy & Lifecycle Lead

Jobstreet Malaysia

Selangor

On-site

MYR 180,000 - 300,000

Full time

14 days+
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Job summary

Jora Malaysia is seeking an experienced Regulatory Affairs professional to lead product registrations and lifecycle management across the Malaysian market. You will develop strategic regulatory plans, navigate submissions, and ensure ongoing compliance with regional and global requirements.

The role requires a strong background in regulatory affairs within pharma or health sectors, coupled with excellent project and stakeholder management skills to support product development and market access

Qualifications

  • Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or related field.
  • Registered Pharmacist (preferred where applicable).
  • 8–10 years of Regulatory Affairs experience in pharma, consumer health, health supplements or traditional medicines.
  • Demonstrated experience developing regulatory strategies and leading product registrations across multiple categories.
  • Experience engaging with regulatory authorities and government agencies.
  • Strong project management, stakeholder management and communication capabilities.

Responsibilities

  • Develop and execute regulatory strategies for product registrations, variations, renewals and lifecycle management.
  • Lead regulatory planning to support commercialization timelines and market launches.
  • Prepare and submit regulatory dossiers with accuracy and compliance.
  • Maintain registrations, licenses and certificates throughout product lifecycle.
  • Monitor regulatory developments and assess impact on business and timelines.
  • Provide regulatory intelligence and strategic advice to internal stakeholders.
  • Collaborate with cross-functional teams and external partners to ensure compliance.

Skills

Project management
Stakeholder management
Communication

Education

Bachelor's degree in Pharmacy

Job description

Jora Malaysia is seeking an experienced Regulatory Affairs professional to lead product registrations and lifecycle management across the Malaysian market. You will develop strategic regulatory plans, navigate submissions, and ensure ongoing compliance with regional and global requirements.

The role requires a strong background in regulatory affairs within pharma or health sectors, coupled with excellent project and stakeholder management skills to support product development and market access

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