Aurobindo Pharma Released Job Openings On 18/07/2022.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 M.Sc with 01-03+ Years Experience for QA / QC Position.Complete Details for the QA / QC  as follows.

Important Details :

• Job Location: Hyderabad/Secunderabad
• No of Vacancies:NA
• Details of Salary:NA
• Opening date for online Application: 18/07/2022
• 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

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Job Description/Skills Required

QUALITY ASSURANCE – API

• 1. Responsible for Batch number generation in ERP System
• 2. Responsible for Review of online monitoring.
• 3. Responsible for Review of Executed BPCR.
• 4. Responsible for Type-II cleaning evaluation & clearance.
• 5. Responsible for Issuance of BPCRs, Documents to all departments.
• 6. Additional Tasks as and when required as assigned in the absence of any person in similar capacity.
• 7. Any other work assigned by HOD/ Designee.
• 8. Attending cGMP trainings and On Job trainings.
• 9. Responsible for stopping of unsafe act in the plant.
• 10. To follow safety Health and Environment norms and adhere with the company policy.

Technical / Behavioral skills:

1. Thorough knowledge on Process and their controls,
2. Domain knowledge, statutory norms
3. Exposure in audits by regulatory bodies
4. Think Strategically, Pursue Innovation, Focus on Quality and Compliance, Drive Execution, Commitment to the customer.
5. Collaborate Actively, Lead and Develop people.

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QUALITY CONTROL – API

• Analytical testing of chemicals, Reagents, Raw materials and other Pharmaceutical products.
• Preparation, Standardization and stability evaluation of volumetric solutions/Reagents/Indicators.
• Performing computerized system validation (CSV) as per current regulatory requirements.
• Ensure/ perform different sampling procedures for chemicals, Raw materials and other Pharmaceutical products.
• Packing, storage and maintenance of retention samples.
• Testing of Raw materials, In-process, Intermediates and APIs using Chromatographic Data system.
• Analytical Testing of Related substances/Content/Assay/Purity testing and Calculation by HPLC Using Empower/Lab Solutions.
• Data generation, Integration and Review of Chromatographic data generated by Chromatographic data system.
• Method Transfers & Holding time Studies.

Click here for Official notification and Apply