About the Company :
The Company has numerous NDA and ANDA with API filings across Europe, south Africa, Canada, Brazil and Australia. Company emphasis on upcoming technology and has many formulation research based centers, with 150 bioequivalent centers around Vadodara, and Gujarat. Initiated state of art R&D center in Hyderabad. Firm is investing around 11% of its profit in its R&D Operation.
Company has pipeline in Oncology products, dermatology, auto immune disorders and injectable formulations.
About the Job :
Experience : 9-12 years
Qualification : B. Pharma/ M. Pharma/ MSc
Experience :
Candidate need to handle the quality control documents like approval, planning and release of testing documents.
Required to release the tested documents after thorough review.
Need to handle the team individually and support during the audits
Should verify the data against the data integrity principles, in the view of regulatory bodies.
Handling of Incidents, Asset management, CAPA, Learning management and Risk assessments, Incidents closure
Need to prepare the monthly planning of QC plan against the manufacturing planning
interested candidates can send the resumes to [email protected]
