Sanofi looking for Executive in Quality Control
Sanofi - aventis, one of the world's leading pharmaceutical companies, is a team of 1,00,000 individuals driven by one common mission to improve people's health and quality of life. Present in more than 100 countries, we are vibrant, people centric, performance driven organization contributing to distinctive healthcare. We invite dynamic enthusiastic individuals to be a part of the team at our state- of- the - art Ankleshwar site, that has set the gold standard in terms of manufacturing plant and processes in the Indian pharmaceutical industry.
Post : Executive Quality Control
Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.
Performing analysis of Raw Material Samples received from new vendors for Pharmaceuticals.
Performing analysis of market complaints, Stability, process validation samples, Cleaning Validation of Pharmaceuticals.
Good Laboratory Practice
Performing calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
Reviewing pharmacopeias for specification preparation.
Preparing SOPs and Formats and Analytical Test Record.
Managing reference standards, working standards, laboratory reagents & chemicals.
Arranging and observing Control Samples and maintaining record.
Participating in Investigation of out of specification results, retesting and review the analysis records. Maintaining & reviewing laboratory raw data related to testing activity. Validation
Preparing protocol for Analytical Method validation, cleaning validation and performing the validation exercise as per the protocol.
Management of laboratory Consumables
Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.
Coordinating with production, and warehouse for analytical activities.
Compliance to HSE Requirements for QC laboratory.
Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.
Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.
Post Graduate in Science (Organic or Analytical Chemistry )
3-4 years in chemical & instrumental testing laboratory with exposure to GMP, GLP.
In Addtion the applicanet should have exposure of working in regulatory enviormnet and display following capabilities.
Co ordination Skill
Exp: 3-4 years
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Quality Control
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