APAC Quality & Regulatory Director

Barrington James

Singapore

On-site

SGD 180,000 - 340,000

Full time

14 days+

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Job summary

Barrington James is partnering with an international life sciences organisation to appoint a Regional Quality & Regulatory Affairs Director responsible for Asia Pacific. You will lead the local QRA team while overseeing regional Quality, Regulatory Affairs and Pharmacovigilance activities.

Your remit includes QMS management, regulatory strategy, GMP/GDP compliance, quality audits, 3PL oversight, warehouse oversight, market authorisations and continuous improvement.

Qualifications

  • More than 8 years' experience across Quality & Regulatory Affairs
  • Pharmaceutical, medical device or IVD experience
  • 3PL and warehouse compliance experience
  • Proven people-management and coaching capability

Responsibilities

  • Lead the APAC QRA team and oversee regional Quality, Regulatory Affairs and Pharmacovigilance
  • Manage QMS, regulatory strategy and GMP/GDP compliance
  • Lead quality audits and third-party logistics oversight
  • Oversee warehouse operations and market authorisations
  • Collaborate with global HQ, local teams and health authorities for continuous improvement

Skills

Quality & Regulatory Affairs
Leadership
Regulatory submissions
3PL compliance

Job description

Barrington James is partnering with an international life sciences organisation to appoint a Regional Quality & Regulatory Affairs Director responsible for Asia Pacific. You will lead the local QRA team while overseeing regional Quality, Regulatory Affairs and Pharmacovigilance activities.

Your remit includes QMS management, regulatory strategy, GMP/GDP compliance, quality audits, 3PL oversight, warehouse oversight, market authorisations and continuous improvement.

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