Senior Manager - P&DD
Sun Pharmaceutical Industries View all jobs
- Halol, Gujarat
- Permanent
- Full-time
- Monitoring of New Product-Packs - Commercial Launches.
- Monitoring of Existing Product-Packs - Revision to comply latest Regulatory / Manufacturing requirement.
- Monitoring of Packaging Process Validation.
- To monitor / carry out documentation related to Packaging Process Development batches (e.g., Feasibility batches, Optimization batches, scale up batches, Stability batches, Pilot bioequivalence & clinical trial batches, Exhibit batches, Registration batches etc.) as per provided plan & checking /review of related documents.
- Facilitation for Procurement and approval of Packaging change parts
- Alternate Vendor Development / Cost effective /Productivity enhancement exercises.
- Packaging documentation for routine as well as continuous technology improvement activities
- Responsible for post launch trouble shooting on ongoing commercial products
- Audit / Inspection related activities.
- Identify need for fresh guidelines & scope of Improvement & drafting relevant guidelines and ensure its implementation.
- Investigation of packaging related market complaints / OOS / OOT / Deviation & implementation of corrective and preventive actions as required.
- SOP creation/revision and implementation.
- Review & approval of SOP.
- Supporting R&D and Plant for technology transfer of Packaging.
- Support and execution of site transfer products.
- Resource planning / Work assignment /Job allocation.
- Ensuring Quality compliance as basis for all documentation.
- Budgeting (Revenue, Capital, IT and Manpower).
- Review and approval of QMS related records from Track wise.
- Exploring Developmental training for subordinate's development.
- Attending CFT and QRB meetings, drawing action plans and ensures its smooth implementation.
- Review & approve the artwork (For filling / trial / commercial product)
- Co-ordinate with CFT's and machine manufacturer to resolve the related issues of packaging machinery.
- Co-ordinate with CFT's and supplier / manufacturer of packaging material to resolve the material related issues.
- Co-ordinate to ensure the URS as per packaging material / current regulatory guidance.
- Co-ordinate to ensure the timely completion of FAT / SAT of new equipment's.
- To ensure the smooth operation of equipment.
- To identify the new equipment as per plant requirement.
- Co-ordinate to ensure the respective documents for smooth operation & filling of new drug product (MPC / Pack Style / EBPR / IBPR / SPEC / ATP).
- To review the trial reports and other developmental documents.