GMP QA Documentation & Compliance Specialist

Lonza; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A global life sciences leader in Singapore is seeking a QA Specialist to oversee quality assurance activities in a GMP Biotech Manufacturing facility. The ideal candidate will have a degree and 3-5 years of relevant experience, alongside a solid understanding of regulatory standards. Responsibilities include supporting daily QA activities, ensuring compliance, and leading projects. This role offers valuable career growth opportunities in a dynamic environment.

Benefits

Comprehensive medical insurance

Company transport to site

Professional growth opportunities

Company transport provided

Qualifications

• 3 to 5 years of experience in a similar industry or role.
• Familiarity with FDA, EMEA, and ICHQ7 standards.
• Able to operate independently.

Responsibilities

• Support QA activities in compliance with SOPs/policies.
• Review and approve SOPs, protocols, reports, and records.
• Lead deviation investigations and CAPA plans.

Skills

Regulatory requirements knowledge

Quality management system experience

Attention to detail

Team player

Safety focus

Education

Degree from recognized institution

Diploma with experience

Job description

A global life sciences leader in Singapore is seeking a QA Specialist to oversee quality assurance activities in a GMP Biotech Manufacturing facility. The ideal candidate will have a degree and 3-5 years of relevant experience, alongside a solid understanding of regulatory standards. Responsibilities include supporting daily QA activities, ensuring compliance, and leading projects. This role offers valuable career growth opportunities in a dynamic environment.