Quality Control Chemist (1 year contract)

AMBITION GROUP SINGAPORE PTE. LTD.; Singapore; On-site; SGD 45,000 - 65,000; Full time

Job summary

A leading recruitment agency in Singapore is seeking a candidate for a role focused on analytical method transfers and technical support in compliance with SOPs and GMP. The ideal candidate holds a degree in Chemistry or Pharmaceutical Sciences and has hands-on experience in a GMP/GLP environment, particularly with HPLC, UPLC, and GC. This position requires strong project coordination skills and attention to detail, with responsibilities including technical documentation and cross-functional collaboration.

Qualifications

• Hands-on experience in analytical method transfer in a GMP/GLP environment.
• Ability to author and review technical documents accurately.
• Strong project coordination skills and detail-oriented.

Responsibilities

• Perform and support analytical method transfers and validations.
• Prepare and maintain technical documentation including SOPs.
• Collaborate with internal teams to manage project timelines.

Skills

Analytical method transfer

HPLC

UPLC

GC

Project coordination

Technical documentation

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