Analytical Chemist I​/II​/III

Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory.

• Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemistry, physical and instrumental techniques such as LC, GC, UV-Vis Spectrophotometer, dissolution, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments.
• Document work clearly and perform tests accurately. Record data and results as specified in documentation procedures.
• Maintain proper laboratory logbooks, notebooks and other records all the time. Report and participate in the deviations and investigations.
• Comply with all regulatory/in-house requirements (may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
• Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by Standard Operating Procedures (SOPs).
• Perform laboratory related other duties as assigned.

• Education:
  
  Bachelor’s Degree in Science/Chemistry
• Experience:
  
  Based on the position level, must require minimum 2-10 years prior experience working in the Quality Control Laboratory in a cGMP environment, preferably in pharmaceutical industry.
• Hands on Empower-3 experience is plus.
• QC experience in Generic Pharmaceutical industries would be preferable
• Knowledge in Good Documentation practices. Knowledge in USP/ FDA

Offers a comprehensive benefits package to employees

• Entry level

• Full-time

• Research, Analyst, and Information Technology

• Pharmaceutical Manufacturing