Dr. Reddy’s Laboratories Hiring Team Member – Production (Quality Focus)

Dr. Reddy’s Laboratories Ltd., a multinational pharmaceutical leader, is seeking applications for the role of Team Member – Production. This position is located at the company’s facility in Visakhapatnam and focuses heavily on quality management and compliance within the Integrated Product Development Organization (IPDO).

Position and Requirements

Detail	Specification
Post Name	Team Member – Production
Location	Visakhapatnam
Qualification	Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, or a related field. (Advanced degree in Pharmaceutical Sciences or Regulatory Affairs is advantageous).
Experience	3-5 years in the pharmaceutical industry, specifically with a focus on product development and quality management.
Functional Area	Production
End Date	November 30, 2025

Key Roles & Responsibilities (Focus on Quality & Documentation)

The successful candidate will primarily handle documentation, quality systems, and compliance within the IPDO environment, including:

SOP Management: Reviewing, revising, and obtaining approval for SOPs (Standard Operating Procedures), and communicating changes across all High-Performance Teams (HPTs).
Document Control: Preparing, reviewing, and approving documents (reports, specifications, Standard Testing Protocols – STPs) generated during product development and technology transfer.
Risk & Compliance: Conducting, reviewing, and approving risk assessments and participating in proposing Quality by Design (QbD) process changes.
Data Integrity & Audits: Exercising control over data integrity, checking filing documentation, reviewing facility/equipment qualifications, and conducting self-inspections at IPDO.
Quality Management System (QMS): Managing quality notifications such as incidents and change controls through the QMS.

Essential Technical Skills

Thorough understanding and practical application of regulatory requirements in pharmaceutical development.
Proficiency in implementing QbD principles.
Expertise in conducting and approving risk assessments throughout the product lifecycle.
Strong focus on ensuring data integrity and compliance with documentation standards.

How to Apply

The advertisement directs candidates to apply by the end date, but does not specify a submission email or portal. Candidates should typically apply through the company’s official careers page or follow internal application procedures if applicable.

Action: You should apply through the official Dr. Reddy’s career portal or the contact provided in the original full advertisement (if available).