Senior Analysis Researcher

Job Description

Job Description:
1) With strong academic and/or industrial background in analytical chemistry, medical chemistry, organic chemistry, biochemistry or other relevant fields.
2) With oversea education background and/or working experience in top pharmaceutical companies; proficient in literature searching and summarization in related working fields.
3) With established working experience in analytical department of pharmaceutical industry.
4) With fluent English language abilities and excellent in working communication with clients of western countries.
5) With abilities of working under pressure and good team collaboration skills; be able to coordinate the team work.
6) Be capable of daily communication with US/EU clients.
7) With strong abilities of self-improvement; keep the space with the requirement of company development and the industrial standards.
8) Be able to write documentations such as protocols and reports clearly and logically.
9) Be good at thinking broadly; be flexible of accepting new things and ideas; be able to make right decisions and discussions promptly.
Requirements:
1) Apply various analytical technologies (i.e. HPLC, LCMS, H-NMP and NOE) on the identification of compounds and structures.
2) Control the process of API production; analyses of raw materials, intermediates and products; in process control of production; set up specifications.
3) Set up the IPC testing methods and stability protocols.
4) Be familiar with method validations and transfer; be knowledgeable with cGMP regulations.
5) Be familiar with CMC and cGMP requirements and be capable of method development/validation for cGMP and API production.

Job Function

Analyst

Salary/Benefits

Negotiable

Desired Skills and Experience

1) Apply various analytical technologies (i.e. HPLC, LCMS, H-NMP and NOE) on the identification of compounds and structures.
2) Control the process of API production; analyses of raw materials, intermediates and products; in process control of production; set up specifications.
3) Set up the IPC testing methods and stability protocols.
4) Be familiar with method validations and transfer; be knowledgeable with cGMP regulations.
5) Be familiar with CMC and cGMP requirements and be capable of method development/validation for cGMP and API production.

Other Jobs From The Same Company

Job Location

Tianjin, China

Job Details

Company:
Mandarin Cafe
Location
  • China: Tianjin
Employment type:
Contract
Languages:
English
Applicants:
Experience:
Industry:
Alternative Medicine
Job ID:
4420

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