Dr. Reddy’s Laboratories: Team Member - Qualification — Visakhapatnam, India

Dr. Reddy’s Laboratories lists a Team Member - Qualification opening in Visakhapatnam, India. The position is listed as full-time. The job description covers compliance, training.

Recruitment overview

OrganisationDr. Reddy’s Laboratories
Post / roleTeam Member - Qualification
Employment typeFull-time
Notification / job IDREF28935F
Job locationVisakhapatnam, India
Work arrangementOn-site
Educational qualificationDegree / qualification: Pharm, M.Pharm, B.Tech, M.Tech
Experience required8 to 12 years overall experience
Salary / stipendSee employer notice for pay details
Last date to applySee official notice

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.

The position and its setting

Dr. Reddy’s Laboratories lists Team Member - Qualification in Visakhapatnam, India, under reference REF28935F. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

  • Employment type: Full-time
  • Employer listing date: 13 October 2026
  • Job Family: Manufacturing
  • Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

  • Job Summary
  • An individual for the qualification team to manage the documentation and execution of qualification activities, including the preparation, review, and execution of various qualification documents
  • The ideal candidate will oversee new project-related tests, review and compile raw data, and ensure compliance with validation master plans and SOPs
  • Additionally, responsibilities include implementing corrective and preventive actions, conducting incident investigations, and providing support during regulatory inspections
  • Be responsible for documentation and execution of qualification activities
  • This includes preparation, review and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ and (Requirement Qualification) documents
  • Your responsibilities include review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems
  • Be responsible for new project related FAT (Factory Acceptance Test) and SAT (Site Acceptance Test)
  • Review: and compile raw data, relevant certificates, analysis test reports and
  • Preparation and review of final summary report
  • Be responsible for preparation and review of protocols and reports for media fill validation and cleaning validation
  • Your role involves initiation of relevant CRN (Change Request Number) for new or existing activity, timely closure of assigned action plans as per CRN, and CRN review and approval
  • Be responsible for corrective and Preventive Action (CAPA) implementation and handling of incident investigations and CAPA related to qualification
  • As part of your role, you will prepare and review VMP (Validation Master Plan)
  • Research / execution: training for employees and external vendors as a qualified trainer
  • Your role includes preparation and review of qualification SOPs (Standard Operating Procedure), conducting investigations as a site investigation team member, and updating Qualification status label

Essential requirements and candidate background

  • Educational Qualification
  • B
  • Pharm, M
  • Pharm, B
  • Tech, M
  • Tech
  • Minimum Work Experience
  • 8 to 12 years overall experience

Location, schedule and contract conditions

  • Work arrangement: On-site
  • Advertised location: Visakhapatnam, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Team Member - Qualification vacancy is not an offer for reference REF28935F; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Dr. Reddy’s Laboratories

Applications follow the official employer page linked below.

Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF28935F.

Compare your qualifications and experience with the essential conditions for the Visakhapatnam, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: compliance

Compliance experience should identify the business process, applicable internal controls and the work you performed. Explain evidence gathering, review, escalation or remediation where those were part of your role.

Relevant skills

  • compliance
  • training

Important links

Official notification / job descriptionOpen official page
Online application portalOpen official page

Read the complete official notice before applying. Availability and requirements can change.

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