QA Supervisor (Pharmaceutical Background)

KINGMAO INTERNATIONAL (S) PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking a QA Supervisor to oversee QA activities and ensure compliance with regulatory standards. You will be responsible for supervising team members, leading investigations, and collaborating with various departments to uphold quality. The ideal candidate will have a degree in a relevant field and 3–5 years of experience in QA, with leadership skills being a plus. The position offers a competitive salary and opportunities for professional growth.

Benefits

A dynamic and supportive team environment

Opportunities for professional growth

Competitive salary and benefits package

Qualifications

• Minimum 3–5 years of QA experience in pharmaceutical or supplement manufacturing.
• Proven leadership or supervisory experience preferred.

Responsibilities

• Supervise and support QA team members on the production floor.
• Ensure compliance with GMP, FDA, and other relevant regulatory standards.
• Lead investigations into deviations, non-conformances, and CAPAs.

Skills

Strong knowledge of GMP

Attention to detail

Communication skills

Education

Degree in Pharmaceutical Sciences, Chemistry, Biology, or related field

Job description

About the Role:

As a QA Supervisor, you will play a key role in supporting the QA Manager, ensuring compliance with GMP, regulatory guidelines, and internal quality systems. You'll be directly involved in supervising QA activities, coordinating inspections, maintaining documentation, and fostering a culture of continuous improvement and accountability.

Responsibilities:

• Supervise and support QA team members on the production floor
• Oversee in-process checks, batch record reviews, and product release procedures
• Ensure compliance with GMP, FDA, and other relevant regulatory standards
• Lead investigations into deviations, non-conformances, and CAPAs
• Collaborate with Production, QC, and R&D teams to uphold quality standards
• Assist in audits (internal, third-party, and regulatory)
• Support training and onboarding of QA personnel

Requirements:

• Degree in Pharmaceutical Sciences, Chemistry, Biology, or related field
• Minimum 3–5 years of QA experience in pharmaceutical or supplement manufacturing
• Strong knowledge of GMP, FDA regulations, and quality systems
• Proven leadership or supervisory experience preferred
• Excellent attention to detail, documentation skills, and communication

What We Offer:

• A dynamic and supportive team environment
• Opportunities for professional growth and leadership development
• Competitive salary and benefits package
• A company committed to quality, innovation, and employee wellbeing