Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP GLP knowledge
Responsibilities
Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples.
Performing analysis of Stability, process validation samples, and Cleaning Validation.
Handling of sophisticated laboratory instruments viz., HPLC, GC, UV IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc.
Valuable Laboratory Practice.
Performing calibration maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment.
Knowledge on the preparation of SOPs and Formats and Analytical Test records.
Managing reference standards, working standards, laboratory reagents chemicals.
Arranging and observing Control Samples and maintaining the record.
Participating in the Investigation of out-of-specification results.
Maintaining laboratory raw data related to testing activity.
Validation
Performing Analytical Method validation, cleaning validation as per the protocol.
Other
Coordinating with production and the warehouse for analytical activities
Compliance to HSE Requirements for QC laboratory.
Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations.
Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities.
Requirements
GMP GLP knowledge
Valuable coordination communication skills.
Analytical ability
Knowledge on LIMS QMS
What makes this position unique
This position will provide positive exposure to work in GMP/ GLP environment.
Location: Ankleshwar, Gujarat, India
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