Dr.Reddys Laboratories Ltd Hiring B. Pharm Fresher / 2024 passout  for Technical Trainee – QA

Dr.Reddys Laboratories Ltd Walk-in Interview 2025.Dr.Reddys Laboratories Ltd Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue… 

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Vacancy details:

• Department: Technical Trainee – Quality Assurance
• Educational qualification: B. Pharm Fresher / 2024 passout
• Minimum work experience: Freshers
• Job Location: Pydibimavaram

Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!

Job Summary
We are looking for an individual for the Quality Assurance team to Preparation and review of APQR, Change control, and CAPA management. Facility and Equipment Qualification management, Facility and Equipment Qualification management, Preparation and review of Quality trends.

Roles & Responsibilities

Preparation and review of Standard Operating Procedure/ Standard Cleaning Procedure / Standard Operating Instructions related to department as well as all functional departments

Facility and Equipment Qualification management, Self-Inspection management, Investigation report review, Preparation and review of APQR, Change control and CAPA management

Preparation, review, and approval of quality risk assessment.

Preparation and review of Site master file and validation master plan

Review of audit trials for GXP systems

Preparation and review of Quality trends like Incidents, Market complaints and CAPAs

Review of process validation protocols/reports, cleaning validation protocols / reports, executed batch records, stability protocols, submission of batch protocols/report, Continuous process verification protocols/reports, Confirmatory/Trial/Pre-validation protocols/ Reports and miscellaneous protocols/ reports

Handling of market complaints and product recalls

Initiation of incidents, review and approval of incidents

Review and approval of the investigations of 1B incidents in absence of reporting manager

Review and approval of all validation / qualification protocols and reports with respect to FAT/DQ/SAT/IQ/OQ/PQ/SLIA/PSQP for facility, area, equipment and utilities

Coordinate and participate in preparation of risk assessment for all new/existing (Subjected to any change) equipment’s/systems/utilities/process

Review of Pest and rodent control records and time synchronization records of equipment

Review of all documents related to GxP systems used for GMP operations / activities

Verification of vendors/third party (Service provider) contract agreement those are required for performing calibrations on specific instruments/Equipment’s on/off site

Organization and co-ordination of QRM activity related to site and Global quality

Participation of validation activities to ensure compliance to approval protocol

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