About this role
The Quality & Regulatory Affairs Director will manage quality, regulatory, and pharmacovigilance activities across the Asia Pacific region while ensuring compliance with international standards. This role involves defining regulatory strategies, maintaining the Quality Management System, and leading the local team to ensure operational excellence.
Candidates must hold a degree in Pharmacy and possess at least 5 years of experience in Quality and Regulatory Affairs within the pharmaceutical or medical device industry. Strong knowledge of GMP, GDP, and ISO standards, along with proven leadership and stakeholder management capabilities, is required.
What they're looking for
Quality Management SystemRegulatory AffairsPharmacovigilanceGMPGDPISO StandardsStakeholder ManagementPeople Management
Frequently asked questions
What does a Quality & Regulatory Director at GRIFOLS, S.A. do?
The Quality & Regulatory Affairs Director will manage quality, regulatory, and pharmacovigilance activities across the Asia Pacific region while ensuring compliance with international standards. This role involves defining regulatory strategies, maintaining the Quality Management System, and leading…
What skills does this Quality & Regulatory Director role need?
Key skills for this role include Quality Management System, Regulatory Affairs, Pharmacovigilance, GMP, GDP, ISO Standards.
How much does a Quality & Regulatory Director at GRIFOLS, S.A. pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Quality & Regulatory Director role remote, hybrid, or on-site?
This role is hybrid, based in Singapore.
How do I apply for this Quality & Regulatory Director role?
You can apply directly on GRIFOLS, S.A.'s careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.