Job Description

DivisionQualityDepartmentDepartment: Corporate Quality AssuranceSub Department: Commercial Complaince and Quality SystemsEmployment TypePermanentJob PurposeMonitor in implementing pharmacopoeial changes, method validation, and cross-functional coordination to ensure regulatory compliance and analytical excellence.Accountabilities

• Review and implementation of pharmacopeial changes across Cipla Locations.
• Responsible for completion of Method improvement , Method verifications and evaluations of Pharmacopoeial Methods.
• Forum stage Assessment for Review and Evaluation of molecules appearing in pharmacopoeia Forum.
• Resolving the issues and queries of the analyst involved in method evaluation and updations of specifications.
• QMS Activity: involved activities of Deviation, CAPA , investigation , Non adoption , comparison of inhouse and pharmacopeia methods.
• Actively connects with cross functional teams like RA , purchase, customer , vendors , and other stake holders for timely implementation of pharmacopeial changes.
• Responsible for submission of Cipla in-house methods to pharmacopoeial commissions.
• Communications with pharmacopeial commission for technical query resolution
• Query Respond and simplification: Follow up done with cross functional Teams to resolve queries and timely implementation. Respond to customer comments on Specification CR.
• Communication with Vendor on adoption of pharmacopeial methods when new changes appeared .
• Sound Knowledge method validation.
• Provide suggestions and ideas by exploring new possibilities to achieve cost saving and work simplification

Education QualificationB.Sc. /M.Sc. (Chemistry)Relevant Work Experience8-10 years of experience in quality control function of a pharmaceutical organisation.Competencies/SkillsCollaborate to SucceedInnovate to ExcelPerform with AccountabilityLead with EmpathyAct with AgilityStrong Domain KnowledgePeople ManagementJob LocationGoaShift Hours

Cipla