Aurobindo Pharma Openings For B.Pharma,M.Pharma Graduates

Aurobindo Pharma Released Job Openings On 05/07/2022.Aurobindo Pharma Limited is an Indian pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Aurobindo Pharma Recruitment 2022 are provided below.

Vacancy Details:

Aurobindo Pharma Hiring B.Pharma,M.Pharma with 10-15+ Years Experience for QA / QC Executive Position.Complete Details for the QA / QC Executive as follows.

Important Details :

• Job Location: Naidupeta
• No of Vacancies:NA
• Details of Salary:NA
• Opening date for online Application: 05/07/2022
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job: Hetero Biopharma Looking For FRESHERS 

QA,QC,R&D,Production,Sales,Packing,RA,Engineering,Medical Coding,Purchase,StoresJobs At Hyderabad,Bangalore,Vizag,Ahmedabad,Mumbai etc 

Job Description/Skills Required

• 1. To review/evaluate the process/material non-conformances, exceptions as per the authorized procedure.
• 2. To co-ordinate with user departments and ensure timely closure of change controls, PNCs and MNCs. and
  market complaint
• 3. To organize and conduct internal audits by using automated QMS software.
• 4. Responsible for co-ordination to regulatory/customer audits.
• 5. Evaluating and trending of PNCs, MNCs, CAPA, Market complaint and Exceptions.
• 6. Responsible for impact/risk assessment and review/evaluate the site Change Controls for approval.
• 7. Co-ordination with QC, packaging development and marketing departments for generation and approval of
  artwork.
• 8. Responsible for investigating the market complaints and queries and responsible for the coordination of product recalls, if any.
• 9. Responsible for scheduling and organizing Quality Review Meetings (QRM) as per stipulated timelines.
• 10. Co-ordinate for the review and revision of SMF/VMP and responsible for the review of the standard
  operating procedures.
• 11. To monitor good documentation practices in the department and conduct cGMP and SOP training.
• 12. Responsible to respond with compliance for regulatory/customer audits.
• 13. To monitor complete review of completed documents and retrieval to QA.
• 14. To follow and implement environmental management systems related procedures.

Click here for Official notification and Apply