Editorial summary

The company seeks a QC Troubleshooting Analyst for its Greenfield Biopharma Plant in the West to lead analytical trouble-shooting investigations and oversee method development, optimization, pre-validation, and transfer of API analysis. The role designs experiments, analyzes data, writes project reports, resolves laboratory technical issues, and provides technical support while leading and training team members to enhance research capabilities. It requires strong expertise in analytical methods, project management, and cross-department collaboration, with the ability to independently manage projects and oversee laboratory operations. The position offers a salary of 8000.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/qc-troubleshooting-analyst-greenfield-biopharma-plant-west-37702 first appeared in Job-Q.com on 13 Oct 2026]

• Lead and coordinate the analytical trouble shooting investigation, and strong understanding the analytical method development / optimization, pre-validation, and transfer of API analysis.
• Design experiments, analyze data, and write reports for projects.
• Resolve technical issues in the laboratory and provide technical support.
• Lead and train team members to enhance the overall research capabilities of the team.
• Communicate and collaborate with other departments and clients to drive project progress.
• Independently manage projects and oversee laboratory operations.
• Keep up with the latest industry technologies and regulatory requirements to ensure compliance with standards.

Qualifications

• Ph.D. or Master's degree in Chemistry, Pharmacy, Analytical Chemistry, or related fields, with at least 2 years (Ph.D.) or 6 years (Master's) of relevant work experience.(open to bachelor as well)
• Proficient in independently operating and maintaining HPLC, GCHS, LC/GC-MS, IC、QTOF、QQQ、ICP、UPCC and other analytical instrumentations.
• Proficient in analytical expertise and familiar with relevant regulations such as ICH, Chinese Pharmacopoeia, USP, EP, etc.
• Rich experience in experimental design and data analysis
• Excellent analytical trouble-shooting skills.
• Strong leadership and team management skills.
• Outstanding laboratory operation skills.
• Excellent time/schedule management and communication skills.
• Fluent in both spoken and written English and Chinese to liaise with internal and external stakeholders in China and overseas.

To learn more about this opportunity, please contact Fiona Koh;  

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R1109239

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