QC Chemist (1 year contract)

AMBITION GROUP SINGAPORE PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A global recruitment firm in Singapore is seeking a qualified individual for a role involving analytical method transfers and validation in compliance with GMP and GLP standards. Candidates should hold a degree in Chemistry or Pharmaceutical Sciences and possess hands-on experience in QC laboratory operations, along with strong knowledge of HPLC, UPLC, and GC. The position demands excellent project coordination skills and the ability to adhere to data integrity and quality standards, making it crucial for organizational success.

Qualifications

• Hands-on experience in analytical method transfer and QC laboratory operations in GMP/GLP.
• Strong practical knowledge of HPLC, UPLC, and GC with troubleshooting skills.
• Ability to author and review technical documents and validation reports.

Responsibilities

• Perform analytical method transfers, testing, and validation.
• Provide technical support for cleaning method development.
• Prepare and maintain technical documentation.

Skills

Analytical method transfer

HPLC

UPLC

GC

Project coordination

Education

Degree in Chemistry or Pharmaceutical Sciences

Job description

Responsibilities

• Perform and support analytical method transfers, testing, validation, and verification in compliance with SOPs, GMP, and GLP requirements.
• Provide technical support for cleaning method development, validation, and post-transfer method support, including equivalency and robustness studies.
• Review and assess compendial monograph updates and evaluate their impact on site products, providing technical and regulatory support.
• Prepare, review, and maintain technical documentation, including SOPs, protocols, reports, position papers, and training materials.
• Support laboratory investigations, deviations, and change controls, ensuring timely and right-first-time delivery of assigned projects.
• Collaborate with internal and external sites to manage project timelines and ensure smooth method transfer and validation activities.
• Ensure compliance with data integrity, GDP, PQS, and laboratory safety, housekeeping, and 5S standards.

Requirements

• Degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Hands-on experience in analytical method transfer, validation, and QC laboratory operations within a GMP/GLP environment.
• Strong practical knowledge of HPLC, UPLC, and GC, with basic troubleshooting capability.
• Familiarity with pharmacopeial and regulatory requirements (USP, JP, EP, ICH).
• Ability to author and review technical documents, SOPs, and validation reports accurately.
• Strong project coordination skills with the ability to manage timelines and work cross-functionally.
• Detail-oriented, safety-conscious, and compliant with data integrity, documentation, and quality standards.

If you have what it takes, please send your resume to [e-mail] or click APPLY NOW. Data provided is for recruitment purposes only. Regrettably, only shortlisted candidates will be notified.
Business Reg No : 200611680D | Licence No : 10C5117 | EA Reg No : R2199023