Aurobindo Pharma Released Job Openings On 22/04/2022.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/B.Sc./M.Sc Graduates With 05-10 year(s) of experience for Production & Manufacturing – Other Position.Complete Details for the  Production & Manufacturing – Other as follows.
Important Details :
- No of Vacancies:NA
- Job Location: Hyderabad
- Details of Salary:Â 5,00,000 – 10,00,000 P.A.
- Opening date for online Application: 22/04/2022
- Mode of application :Online
- How To Apply: please share your Updated cv on shankarnag.sipureddy@aurobindo.com
Related Job:Â Macleods Pharmaceuticals Hiring In Production,Q.A,QC,Warehouse DepartmentsÂ
Job Description/Skills Required
- Pvides leadership, mentoring and development opportunities for the IPQA staff.
- Ensures IPQA are appropriately trained and aligned to support plant operations.
- Aligns with site goals and ensures IPQA staff is supporting Quality, Compliance and Production objectives, focused on Quality Throughput.
- Provides Strategic direction to the In-Process QA group in alignment with site and QA objectives, to ensure that business and compliance needs are met.Ensure the IPQA staff is available and active in first response to product quality issues for all shifts.
- Ensures product, facility, and equipment holds are placed when batch, equipment or systems are potentially impacted.
- Provide Line clearance in every step of manufacturing prior to commencement of manufacturing and during change over.
- Ensure the materials are dispensed as per the standard quantities mentioned in the BMR.Online checking of In-process parameters.
- Carry out sampling of In-process, Finished Product, Stability and Retention samples for the commercial and validation batches after receiving intimation from production department and submitting to QC.
- Online Review / Checking of Batch Manufacturing and Batch Packaging Records.
- Ensure the process is being manufactured as per the BMR & BPR.
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