Freshers BPharma QA Trainee Jobs at Dr. Reddy’s Labs

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Freshers BPharma QA Trainee Jobs

Freshers BPharma QA Trainee Jobs at Dr. Reddy’s Labs

Technical Trainee – Quality Assurance

Location: Andhra Pradesh, India

Dr. Reddy’s Laboratories

Job Description

Job Summary:

We are looking for an individual for the Quality Assurance team to handle preparation and review of APQR, Change Control, and CAPA management. The role includes 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 the department and 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 assessments.
  • Preparation and review of Site Master File and Validation Master Plan.
  • Review of audit trails for GxP systems.
  • Preparation and review of quality trends such as incidents, market complaints, and CAPAs.
  • Review of process validation protocols/reports, cleaning validation protocols/reports, executed batch records, stability protocols, submission batch protocols/reports, 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 investigations of 1B incidents in the absence of the 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 the preparation of risk assessments for all new/existing (subject to any change) equipment/systems/utilities/processes.
  • 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 vendor/third-party (service provider) contract agreements required for performing calibrations on specific instruments/equipment on/off-site.
  • Organization and coordination of QRM activity related to the site and global quality.
  • Participation in validation activities to ensure compliance with approved protocols.

Qualifications:

  • Educational Qualification: B. Pharm Fresher / 2024 Passout.
  • Minimum Work Experience: 0-1 year of experience in the pharmaceutical industry, with a focus on quality management and engineering assurance.

Skills & Attributes:

Technical Skills:

  • Thorough understanding of handling QMS events, self-inspection management, investigation report review, and preparation and review of APQR.
  • Experience in review and approval of all qualification/validation activities.
  • Expertise in conducting, reviewing, and approving risk assessments.
  • Strong focus on ensuring data integrity and compliance with documentation standards.

Behavioural Skills:

  • Effective communication skills to relay SOP changes and ensure understanding across cross-functional teams.
  • Meticulous attention to detail for reviewing all documentation activities.

APPLY ONLINE HERE

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