Monitor the API, formulated products against stipulated conditions mentioned in the batch production record. Conduct certification of batch production records for compliance and stage wise completion.
To review and assess data based on Analytical QBD based approach. To ensure analytical development data supports to robust test method and suitable to entire product lifecycle.
Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications to the world. We are hereby inviting candidates who are interested to join India's No. 1 company in Pharmaceutical sector.
Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications to the world. We are hereby inviting candidates who are interested to join India's No. 1 company in Pharmaceutical sector.
To design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and impurities.
Sun Pharmaceutical Industries limited is the largest specialty generic pharmaceutical company in the world. We provide high quality, affordable medicine trusted by healthcare professionals and patients in over ISO countries. It is also India's largest, most trusted and most valuable pharmaceutical company by market capitalisation.
Experience in IPQA, Process & Cleaning Validation, Media fill Air- flow study, Continuous process verification, Batch release, Finish product sampling,Shop floor activities
Compile registration dossiers for submission to various health authorities like – US, Canada, Europe, Australia. Prepare responses to deficiency letters received from various agencies.
Literature search, product understanding, data interpretation for product to be undertaken for development. Initiation of documents required for product development/movement like T-License, Import License for drug substance as well as reference product and bioequivalence study request.