Research Associate



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Job Type




Salary Range

Up to USD0.00 per year

No. of Openings


Branch Information

Manpower Engineering ,


Job Description

Job Description:

Perfonn analytical method development, verification, validation and testing using a wide variety of analytical techniques, such as HPLC. GC, FTIR, UV, TGA/DSC etc.

Independently set up and operate analytical instrumentations and perform troubleshooting as needed.

Write study protocols and prepare summary technical reports.

Review data, notebooks, and reports to ensure compliance with specifications, standard operating procedures, and regulatory requirement.

Communicate and present results to supervise/mangers.

Expertise: Knowledge & Skills:

Hands-on experience in analytical technologies, including HPLC, GC, UV, FTlR, etc. is required.

Experience in analytical method development/validation, troubleshooting, optimization and transfer to QC.

Requires working knowledge of professional field and phannaceutical industry in cGMP and/or R&D environment.

Proficiency with Microsoft Office Applications (e.g. Word, Excel, Power Point).

Working knowledge of chromatography data systems (e. g. Empower) is highly preferred.

Knowledge of cGMP, regulatory guidelines such as FDA and ICH guidelines.


A Ph. D or MS degree in analytical chemistry, organic chemistry, or related scientific discipline.

Pharmaceutical Industry or a relevant post-doc experience of 0-4 years for Ph.D., 3-6 years for M.S. candidates.

Minimum two years' experience in pharmaceutical industry.

A strong fundamental understanding of chemistry principles.

Ability to meet deadlines and be able to work independently.

Strong communication interpersonal skills and good technical writing skills