QC / Analytical Development Scientist | Greenfield Biopharma Plant | West

• 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; [email protected]

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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