Manger 1
SUN PHARMA ADVANCED RESEARCH COMAPNY
18 March 2016 —
To date
1)Led AMT to QC and Contract manufacturing facilities
2)To ensure on handling of documents like ATP, specification, stability protocol, sampling directory from initiation till implementation
3)To ensure a timely and effective communication & escalation process exists to raise quality issues to appropriate levels of management
4)Monitoring of analysis and planning of work to be carried out in Exhibit stability & Commercial QC Lab for NCE molecules
5) To involve in investigation and to collaborate with CFI team for root cause determination and implementation of effective CAPA
6)Monitoring of stability batches-Annual, commercial, clinical and filing
7)Managing the team including mentoring and coaching of staff, establishing priorities and delivering project within budget on time.
8)Use a team-oriented approach to problem resolution
9)Responsible for carrying out any other responsibilities assigned
10)To participate in Laboratory internal audit, customer audit, Health authority inspection
11)Drove regulatory compliance initiatives, ensuring audit readiness and data integrity