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Orion Pharma logo
Executive - Analytical Orion Pharma

0.0 years

0 Lacs

hyderabad, telangana, india

On-site

Job Description The role will have the following responsibilities: Responsible for planning stability studies, writing and/or review of stability protocols, reports, and preparation of technical documents in CTD format. Co-ordinate and follow up stability studies at contract research organizations (CROs)/ Chemical Quality Control lab of Orion (CQC). Co-ordinate and follow up validation and method transfer at CROs. Write/check/review analytical and pharmaceutical documents as per regulatory requirements (method and validation documents/ variations/ additional question responses) Evaluate/ review method validation protocols / reports / analytical methods prepared by CROs. Reviewing and comment...

Posted 1 week ago

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