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GMP Coordinator - Officer/Executive job at Zydus Cadila

By: Jobs | Views: 185 | Date: 17-Feb-2016

GMP Coordinator - Officer/Executive job at Zydus Cadila for 3 to 6 year Experience.

Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted revenues of over Rs. 8600 crores in FY15. The group had posted a turnover of Rs. 4600 crores in FY 11, making it a billion dollar company. It aims to be a leading global healthcare provider with a robust product pipeline and aspires to post revenues of Rs. 10000 crore by 2015-16 and be a research-based pharmaceutical company by 2020.
DesignationGMP Coordinator - Officer/executive
Job Description1. Reading of Standard Operating procedures (SOPs) to understand and to perform the activities as per Good manufacturing Practices and Safety norms

2. Maintaining of Training card.

3. Ensure for checking of daily activities as per SOP like Balance calibration / Verification, Cleaning & Sanitation, Differential pressure recording, return filter cleaning etc.

4. Ensure that Equipment status Boards of equipment are maintained by shift personnels as per current status.

5. Witness the critical activities in the processes in relevant documents by self / shift personnels.

6. Ensure that shift personnels are following checking of Raw Material quantities, B.No / Lot number, physical appearance , Equipment cleanliness, functionality and Instruments, availability of Utility prior to start operations.

7. Ensure deviation / incidents are recorded in the Quality system by staff personals of shifts if deviation / incidents occurred during operation / execution.

8. Investigation of deviations, incidents, OOS, OOT and implementation of Corrective Actions and Preventive Actions.

9. Initiation of Change control, CAPA and its implementation within the time line.

10. Issuance , Check and Ensure that Raw material , packaging material and cleaning material is received as per requirement mentioned in material requisition slip from warehouse and keep it to the designated area in plant.

11. Documents like BMR / ECR / SRR review after completion of activity and submission to QA.

12. Ensure maintaining of plant and its surrounding area cleaning in every shift & every day.

13. Ensure the availability of BMR , Equipment Usage log book updated on-line near the relevant equipment / place by shift staff.

14. Planning of Equipment Preventive Maintenance as per Preventive Maintenance scheduled.

15. To ensure self, staff and operators adherence to GMP & safety norms.

16. Awareness & compliance of cGMP, Safety, SAP etc.

17. Focus for improvement in day to day activity.

18. Awareness about Energy Conservation like Electricity, water, manpower etc.

19. To impart on job training regarding standard operating procedures and cGMP norms.

20. Coordination with interfacing department like Engineering, QC, QA, Safety, Warehouse etc.

21. To create discipline in the plant w.r.t. Regularity, leave management, shift re-arrangement, safety and GMP.

Desired ProfilePlease refer to the Job description above
Experience3 - 6 Years
Industry TypePharma / Biotech / Clinical Research
RoleProject Manager-Production/Manufacturing/Maintenance
Functional AreaProduction, Manufacturing, Maintenance
Education

UG - B.Sc - Chemistry

PG - M.Sc - Chemistry

Doctorate - Doctorate Not Required

Compensation: Not disclosed
LocationVadodara/Baroda
KeywordsGMP documentation Change Control Deviation OOS
ContactMs. Hiral Shah 
Cadila Healthcare Limited 


For Apply visit:
http://www.naukri.com/joblistingsGMPCoordinatorOfficerexecutiveCadilaHealthcareLimitedVadodara-Baroda-3-to-6-years-100216001807





















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