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Jobs in Singapore   »   Jobs in Singapore   »   Regulatory Affairs Manager, APAC (Healthcare/ Pharmacuetical)
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Regulatory Affairs Manager, APAC (Healthcare/ Pharmacuetical)

Michael Page International Pte Ltd

Michael Page International Pte Ltd company logo
  • Global Market leader in the Healthcare Industry
  • Regional opportunity, dynamic and professional development-oriented environment

About Our Client

The client is a global leader in the pharmaceutical and healthcare industry, renowned for its commitment to providing life-saving medications and innovative medical devices. The APAC HQ is based in Singapore. With a focus on delivering high-quality products and services, they strive to improve patient outcomes and enhance healthcare worldwide. They are currently expanding their team and is looking for a Regional Regulatory Affairs Manager, covering the APAC regions.

It is a newly created opportunity, preferably someone with Regional Regulatory Affair experience within the pharmaceutical/ healthcare industry.

Job Description

  • Develop and implement regulatory strategies to ensure compliance with regional regulations and guidelines for product development, registration, and marketing
  • Lead regulatory submissions and interactions with health authorities to obtain and maintain approvals for pharmaceutical products within the designated region
  • Stay abreast of regulatory changes and assess their impact on product development and commercialisation strategies
  • Collaborate cross-functionally with internal teams, including Quality Assurance, and Commercial etc. to support regulatory requirements and timelines
  • Provide regulatory guidance and expertise to stakeholders on regional regulatory requirements and best practices
  • Provide guidance, support and mentorship to regional regulatory affairs team to ensure effective execution of regulatory activities

The Successful Applicant

  • Bachelor's degree in Life Sciences, Biology, Pharmacy and related disciplines
  • Demonstrated experience in regulatory affairs within the pharmaceutical industry, with a focus on regional regulations
  • Strong knowledge of regulatory requirements and processes for registration and post-market compliance
  • Proven ability to lead regulatory submissions and engage with health authorities effectively
  • Excellent communication, negotiation, and problem-solving skills

What's on Offer

  • Attractive renumeration package
  • Great career prospects with regional opportunity
  • Healthcare industry with great culture and environment
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