Post Graduate in Science (Organic or Analytical Chemistry) or B.Pharm/M.Pharm
8-10 years in chemical & instrumental testing laboratory with exposure to GMP,
GLP
Technical skills &
Competencies / Language
* Analytical ability
* Trouble shootings
* Co ordination
* Communication
* Problem solving
JOB PURPOSE
Generic
Implement quality control activities for Pharmaceuticals at Ankleshwar adhering
to regulatory / global quality Directives and HSE guidelines with optimum
utilization of resources to ensure consistent good quality of products to meet
with customers’ requirements, living Group’s Values and Code of Ethics.
KEY ACCOUNTABILITIES
Testing
Performing and organizing timely analysis of raw material, bulk product,
intermediates, finished goods and other samples for Pharmaceuticals.
Performing and organizing analysis of market complaints, Stability, process
validation, Cleaning Validation samples of Pharmaceuticals.
Valuable Laboratory Practice
Performing and organizing calibration / maintenance of lab. Equipment and
assisting for the qualification of laboratory equipment.
Reviewing pharmacopeias for specification preparation.
Preparing SOPs, Formats, Specification, Analytical Test Record and other
documents.
Managing reference standards, working standards, Laboratory chemicals &
reagents.
Managing instrument laboratory with reference to spares, maintenance etc.
Managing Control Samples and related record.
Approval / Rejection of Raw Materials, Packaging materials, in process
materials, Bulk Finished products and bulk medical device.
Investigating out of specification results, retesting and review the analysis
records.
Maintaining & reviewing laboratory raw data and log book related to testing
activity.
Responsible for reviewing the chromatographic data.
Validation
Preparing protocol and report for Analytical Method validation, cleaning
validation an