Company Introduction
Exemed Pharmaceuticals is a research-driven pharmaceutical manufacturer focused on the development and supply of high-quality active pharmaceutical ingredients from its Vadodara facility, operating under global regulatory approvals.
Core Responsibilities
- Perform chemical testing on raw materials, in-process samples, intermediates, and finished API samples using validated laboratory instruments.
- Operate HPLC and GC systems to generate chromatograms for routine analysis and stability studies.
- Prepare analytical worksheets, test reports, and instrument logbooks in line with GMP documentation requirements.
- Conduct system suitability checks, calibration, and verification of analytical equipment before sample analysis.
- Support laboratory investigations by generating analytical data for OOS and OOT reports using approved methods.
- Assist regulatory and customer audits by presenting laboratory records, chromatographic data, and test summaries.
Skills & Technical Exposure
- High Performance Liquid Chromatography systems and associated detectors.
- Gas Chromatography instruments used for impurity and residual solvent analysis.
- Chromeleon software version 7.2 for data acquisition and processing.
- Wet chemistry testing methods as per pharmacopeial specifications.
- GMP analytical worksheets, logbooks, and controlled laboratory documents.
- Stability chambers and related sample tracking records.
Experience Context
- Work is carried out in a regulated quality control laboratory within an API manufacturing plant.
- Daily handling of multiple samples across different batches ensures uninterrupted product release cycles.
- Analytical instruments are shared across studies, requiring disciplined scheduling and documentation.
- Absence of this role would delay batch disposition, stability evaluation, and regulatory reporting.
How to Apply
Interested candidates may apply by sending their resume to recruitment@exemedpharma.com
