Job Description

POSITION SUMMARY:

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

MAJOR DUTIES/RESPONSIBILITIES:

• 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.

MINIMUM/PREFERRED REQUIREMENTS:

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

BENEFITS: Offers a comprehensive benefits package to employees

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