Aurobindo Pharma Walk In Interview 2023. Aurobindo Pharma Notification full details below. Interested and eligible candidates can Send Resume To HR mail .Founded in 1986 by Mr. P. V. Ramprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born of a vision. The company commenced operations in 1988-89 with a single unit manufacturing Semi-Synthetic Penicillin (SSP) at Pondicherry.
Vacancy details:
- Department:– Quality Assurance (QMS) – Executive / Senior Executive (Formulations – OSD)
- Qualification: B.Pharma in Any Specialization/M.Pharma in Pharmacy
- Experienced: 05-10 yrs
Job Description: Greeting from Aurobindo Pharma !!!!
Important Details :
- Location: Naidupeta
- Post of date:20/01/2023
- Selection Process: The selection will be on the basis of Interview.
We are looking for Quality Assurance (QMS) – Executive / Senior Executive (Formulations – OSD) for Naidupeta , Andhra Pradesh. (60 KMS from Thirupathi, 70 KMS from Nellore)
Roles and Responsibilities :
- To monitor and to trace the Change controls, Exceptions, Process Non Conformances and Material Non Conformances in Quality Management System.
- To coordinate with other departments and to ensure all the Change controls, Exceptions, Process Non Conformances and Material Non Conformances for the closure within due date.
- Responsible for all the change control coordination activities.
- Conducting and organize internal audits with coordination of various departments by using automated Quality Management System software.
- To initiate, review the Corrective action & preventive actions and to coordinate with other departments for its closure within due date.
- Handling of Market complaints.
- Involving in Root cause analysis, Failure Investigations and Risk assessment activities.
- To maintain all the Quality Management System documentations.
- Coordination with customers for approval of change controls and approvals in Quality Management System module.
- To prepare and review of the Standard Operating Procedures and to ensure their implementations
- To prepare and review the trends for Change controls, Process Non Conformances and Material Non Conformances, Exceptions and Corrective action & preventive actions.
- Monitoring of Good Documentation Practices in the departments.
- Conducting current Good Manufacturing Practices training.
- Responsible for the preparation of response to the observation made by the regulatory authorities /customers.
- To support for the preparation of annual product review.
- To support for the document management system.
- To follow and ensure compliance on Environmental Management Systems related procedures.
- To follow the laid down Quality Culture principles and behaviors.
- Any other departmental activity assigned by Head of the Department or his designee.
Desired Candidate Profile :
Ideal candidate should be a B.Pharma or M.Pharma with 05 to 10 years of experience from FDA regulated plant is needed for this role
Preference will be given only to candidates who are Formulations – OSD background
Perks and Benefits :Salary will be best and based on candidate caliber and competency.
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