Job Description

Key Responsibilities

Perform routine and non-routine analysis of pharmaceutical finished products, and stability samples using

HPLC, GC, Dissolution

, and other analytical techniques Ensure all testing is carried out in compliance with GMP, SOPs, and regulatory requirements Accurately document all analytical data, observations, and deviations in accordance with ALCOA+ principles Perform equipment calibration, qualification, and routine maintenance as required Troubleshoot analytical methods and instruments, and escalate issues when necessary Assist in method development and method transfer activities where applicable Support laboratory investigations, OOS, and deviation reports with technical input Provide support and guidance to junior analysts and contribute to their technical development Maintain lab cleanliness, safety, and regulatory compliance at all times

Occasional Duties

Perform routine analysis of finished products for physical parameters, including: Average Weight, Uniformity of Weight, Disintegration, Friability, Hardness, Water content by Karl Fischer (KF),Identification tests (chemical, UV, IR),Loss on Drying (LOD), and product Description

Candidate Requirements

Minimum Qualifications & Experience:

A relevant science degree (e.g., Chemistry, Pharmaceutical Sciences, Biochemistry, etc.) Minimum of

6

years of experiencein a GMP-regulated pharmaceutical testing laboratory Strong hands-on experience with

HPLC, GC, and Dissolution

is essential

Essential Skills:

Sound understanding of analytical chemistry principles and GMP compliance Familiarity with analytical instruments and software (e.g., Empower, Chromeleon) Good organizational, communication, and problem-solving skills Ability to work independently and collaboratively in a fast-paced environment
Job Type: Full-time

Pay: 25,500.00-27,500.00 per year

Benefits:

Free parking On-site parking
Work Location: In person