Company Introduction
Immacule Lifesciences develops and manufactures pharmaceutical products with controlled quality systems at its industrial facilities.
Core Responsibilities
- Review analytical test reports generated from chromatographs and laboratory worksheets.
- Examine calibration records of balances, pH meters, and analytical instruments.
- Authorize laboratory control documents covering raw material, packing material, and finished samples.
- Check stability study data files maintained for long term and accelerated conditions.
- Verify laboratory investigation records stored for out of specification and atypical results.
- Approve certificate of analysis data entered within laboratory information management systems.
Skills and Technical Exposure
- High performance liquid chromatography and gas chromatography systems.
- Laboratory information management systems used for data recording.
- Analytical method validation protocols and reports.
- Calibration schedules and instrument qualification documents.
- Pharmacopoeial specifications and in house analytical procedures.
Experience Context
- Work location is a quality control laboratory supporting a pharmaceutical manufacturing plant.
- Daily sample load covers raw materials, in process samples, finished goods, and stability pulls.
- Without this role, laboratory data approval halts batch disposition timelines.
How to Apply
recruitment@immacule.in