- Location: Singapore / Malaysia
- Industry: Pharmaceuticals, Biologics, CDMO, Life Sciences Manufacturing
Job Details
We are engaging with experienced Quality and GMP professionals for confidential and upcoming opportunities with international pharmaceutical and life sciences organizations expanding their technical and compliance capabilities across Southeast Asia.
This role would suit a Quality professional with strong exposure to GMP manufacturing, quality systems, audits, deviation management, CAPA, validation, and regulatory inspection readiness.
Key Responsibilities
- Lead and strengthen GMP quality systems across manufacturing or technical operations environments.
- Support internal and external audits, regulatory inspections, and quality improvement initiatives.
- Oversee deviation investigations, CAPA effectiveness, change control, and quality risk management.
- Partner with production, engineering, validation, supply chain, and regulatory teams.
- Drive continuous improvement in compliance, documentation, and inspection readiness.
Job Requirements
- Degree in Pharmacy, Chemistry, Life Sciences, Biotechnology, Engineering, or related discipline.
- 8+ years of experience in pharmaceutical, biologics, API, formulation, or CDMO environments.
- Strong knowledge of GMP, GDP, ICH, validation, and quality systems.
- Experience dealing with regional or international regulatory expectations will be advantageous.
Suitable for Senior QA Managers, Quality Systems Managers, GMP Compliance Managers, or Site Quality Leads.
Interested?
Please be advised that due to the considerable number of applications we receive, we are only able to contact candidates who meet our client’s requirements.
We appreciate your understanding and wish you the best in your career endeavors.
Sathiyarajan Vinayagamani – SaVi
EA Personnel KAH Reg No: R1216080
EA License No: 23C1889
