Intas Pharmaceuticals Ltd Issued Job Opportunities

Intas Pharmaceuticals Ltd is Hiring for Executive – Quality Assurance and has issued notification to accept Applications.Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon..Application form link provided at the end of post. 

Vacancy summary details :

• Company Name: Intas Pharmaceuticals Ltd
• Location : Ahmedabad
• Post Name: Executive – Quality Assurance 
• Qualification:  B.Pharma,M. Pharma
• Experience: 5 years
• No of Vacancies: NA
• Details of Salary: NA
• Closing date for online Application : Apply as soon as possible
• Date of examination: NA
• Time and Venue :NA
• Mode of application : online
• Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 

1. Maintaining job description and training record

2. To ensure the compliance as per GMP requirement.

3. To participate in the implementation and monitoring of quality system.

4. To review the quality standard in line with regulatory requirement.

5. To participate the failure mode effect analysis activity.

6. To prepare and review the FMEA report and track the identified actions for completion.

7. To coordinate the activity for closure of FMEA.

8. To maintain track of qualification and validation activities.

9. To prepare and review the protocols and reports. Execution of various qualification / validation activities.

10. To review correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ, FAT)

11. Co-ordinate with production and other user department for qualification/validation activities.

12. Timely compile and review of qualification validation reports.

13. To review the equipment documents like calibration reports and ensure correctness of documents.

14. To perform FAT.

15. To co-ordinate with outside agencies for execution of qualification activity whenever required.

16. Identification of deviation through review and observation

17. To prepare annual Re-qualification/validation schedule, update VMP and Qualification related SOPs as and when required.

18. Review of day to day and online compliance. Ensure compliance of GMP in validation/qualification section.

19. Any other job assigned by department Head.

20. Stick adherence to health, safety and environment

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply