Posted:1 day ago|
Platform:
On-site
Full Time
Followings will be the Job Responsibilities of the position holder: 1. To initiate Change Control and perform impact assessment. 2. To perform manufacturing investigations related to deviation / OOS / OOT and market complaints to identify the root cause and implementation of appropriate CAPAs. 3. To ensure the compliance of quality notifications like deviations and investigations for proper closure. Review of non-conformances, deviations, change controls, internal audits, annual product quality reviews and to perform assessment on other impacting documents and related activities. 4. Handling of Track wise software, SAP and Documents compliance software’s. 5. To perform and participate in Quality risk management exercises whenever required. 6. To perform the gap analysis with respect to cGMP guidelines, current regulatory requirements, and SOPs, wherever required and to comply with the requirements and implement the same. 7. To ensure proper training to all the concerned personnel with respect to investigation outcomes. 8. To ensure compliance at shopfloor with respect to SOPs. 9. Preparation and review of Standard Operation Procedure. 10. To follow the environmental, health and safety policy of organization. 11. To perform any other task as assigned by the department manager.
Abbott Laboratories
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Ahmedabad
3.0 - 4.0 Lacs P.A.
Ahmedabad
3.0 - 4.0 Lacs P.A.
Pune, Maharashtra, India
Salary: Not disclosed
Ahmedabad, Gujarat
Experience: Not specified
Salary: Not disclosed
Pune, Maharashtra, India
Experience: Not specified
Salary: Not disclosed
Velachery, Chennai, Tamil Nadu
Experience: Not specified
Salary: Not disclosed
Pune, Maharashtra, India
Salary: Not disclosed
Ahmedabad, Gujarat
Experience: Not specified
Salary: Not disclosed