4 - 9 years
4 - 8 Lacs
Posted:1 week ago|
Platform:
Work from Office
Full Time
1. Drive product robustness for all products in area of responsibility and lead the third party operation team.
2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities.
3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs.
4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to transfers of Drug Product Manufacture and Packaging.
5. Be familiar with statistical tools to analyze data.
6. Provide third party and techno-commercial leadership in the areas of production and packaging process and process optimization using pharmaceutical processes.
7. Knowledge of all pertinent technical information related to an assigned product.
Detailed knowledge of the operation, maintenance, and utility of all manufacturing and/or packaging equipment for assigned projects. Thorough familiarity with cGMPs, SOP's, relevant government regulations, and current industry standards.
8. Responsible for Techno-commercial activities for all dosage form.
9. Responsible for Sourcing / coordinate with LL/TP manufacturers for product related documents.
10. Supplier Identification:
• Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for markets.
11. Supplier Qualification and Onboarding:
• Developing and implementing a robust supplier qualification process to ensure that selected suppliers meet the necessary standards and regulations in coordination with quality team.
PHARMA
THANKS YOU
REGARDS
MILAP RATHOD (7486829377) call or whtup
HR DEPARTMENT
OPES HEALTHCARE PRIVATE LIMITED
Opes Healthcare
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