Director of Regulatory Affairs and Quality

Regional Quality & Regulatory Affairs Director

Great Quality & Regulatory Affairs leaders do more than maintain compliance.

They build capable teams, influence stakeholders, anticipate risk and create standards that enable the business to perform at its best.

We are partnering with an international life sciences organisation to appoint a 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 will include QMS management, regulatory strategy, GMP/GDP compliance, quality audits, third-party logistics, warehouse oversight, market authorisations and continuous improvement.

You will work closely with global headquarters, local teams, external partners and health authorities, making this an excellent opportunity for a leader who enjoys both people development and technical ownership.

You should bring:

• Degree in Pharmacy

• More than 8 years experience across Quality & Regulatory Affairs

• Pharmaceutical, medical device or IVD experience

• Strong GMP/GDP/ISO knowledge

• 3PL and warehouse compliance experience

• Proven people-management and coaching capability

• Excellent stakeholder-management skills

If you are looking for a role where your leadership can make a genuine regional impact, I would love to hear from you.

CEI: R2090154 | Licence No.: 22S1313