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: Bachelors 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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