QC Analyst III | Pharma Industry

TG Singapore; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company in Singapore seeks a skilled QC Analyst with 3–6 years' experience. You'll support analytical testing, stability programs, and GMP compliance to ensure the timely release of pharmaceutical products. The ideal candidate will possess hands-on experience with cGMP practices and strong documentation skills.

Qualifications

• 3–6 years of hands-on experience in a GMP pharmaceutical QC lab setting.
• Knowledge of analytical techniques such as HPLC, GC, UV, FTIR.
• Proven ability to document results accurately and follow SOPs.

Responsibilities

• Perform routine and non-routine testing of raw materials and pharmaceuticals.
• Manage sample storage and execute stability testing.
• Participate in deviation investigations and audits.

Skills

Analytical Testing

cGMP Practices

Strong Documentation Skills

Team Collaboration

Attention to Detail

Education

Diploma or Bachelor's degree in Chemistry or Pharmaceutical Sciences

Tools

HPLC

GC

UV

FTIR

LIMS

Job description

Job Summary:

We are seeking a skilled QC Analyst with 3–6 years of experience in pharmaceutical quality control laboratories. This role will support analytical testing, stability programs, and GMP compliance activities to ensure the integrity and timely release of pharmaceutical products and materials. The ideal candidate will have hands-on experience with cGMP practices, analytical instrumentation, and strong documentation skills.

Key Responsibilities:

• Analytical Testing: Perform routine and non-routine testing of raw materials, intermediates, drug substances/products, packaging materials, and complaint samples.

• Stability Programs: Manage sample storage, execute stability testing, and ensure documentation complies with regulatory standards.

• Compliance & Documentation: Ensure activities are aligned with cGMP/cGLP, ALCOA+ principles, and data integrity requirements.

• Equipment Management: Operate, calibrate, maintain, and qualify laboratory instruments and systems.

• HSE & Lab Safety: Follow health, safety, and environmental guidelines; proactively identify and mitigate risks.

• Support Investigations: Participate in deviation investigations, CAPAs, and audit readiness.

• Collaboration: Work cross-functionally with QA, production, and R&D for continuous improvement and issue resolution.

Requirements:

• Diploma or Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.

• 3–6 years of hands-on experience in a GMP pharmaceutical QC lab setting.

• Knowledge of analytical techniques such as HPLC, GC, UV, FTIR, etc.

• Experience with LIMS and other quality systems (preferred).

• Strong understanding of regulatory requirements (FDA, EMA, ICH).

• Proven ability to document results accurately and follow SOPs.

• Strong attention to detail and commitment to quality.

• Good communication and teamwork skills.

To Apply, please kindly email your updated resume to [e-mail]

Regret to inform that only shortlisted candidates will be notified.

CEI: R25127749

EA License: 14C7275