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

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 Qualifications in Visakhapatnam, India, under reference REF28709V. 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: 5 October 2026
• Job Family: Manufacturing
• Brands: Dr Reddy's Laboratories Limited

Responsibilities and work described

• Job Summary
• This role is for a Qualification & Validation Specialist responsible for executing equipment and system qualification protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
• The position involves coordinating with vendors and cross-functional teams, preparing risk assessments, SOPs, validation programs, and master plans, and ensuring compliance with cGMP standards
• Contribution: to regulatory readiness by compiling qualification documents, supporting audit responses, and coordinating CAPA, incidents, and deviations
• The role emphasizes safety risk assessments, digital system implementation (eVal), and vendor audits
• Additionally, you will assist in preparing corrective actions, drive safety awareness, and support continuous improvement in qualification and validation practices
• Be responsible for executing qualification protocols (IQ, OQ, PQ), coordinating with vendors and cross-functional teams
• Be responsible for compiling qualification documents, preparing risk assessments, SOPs, validation programs, and master plans
• Be responsible for executing equipment requalification as per schedule and updating qualification schedules
• Be responsible for assisting in audit responses, coordinating with QA for CAPA, incidents, deviations, and audit reports
• Be responsible for preparing master documents (SOPs, operating instructions, VMPs) and coordinating risk assessments for equipment/systems
• Be responsible for assessing safety risks, driving implementation of safe procedures, and creating awareness among team members
• Be responsible for supporting digital system implementation (eVal) and coordinating URS, DQ, and quantitative risk assessments with production and engineering
• Be responsible for coordinating with QA and engineering for cGMP document approvals and vendor audits

Essential requirements and candidate background

• Educational qualification: Graduation in Pharmacy, Science, Mechanical Engineering, Chemical Engineering, Industrial Engineering, Electrical Engineering, Biotechnology or related field is mandatory
• Minimum work
• 8 to 10 years of experience
• Skills & attributes &Critical exposures
• Functional Skills
• Calibration
• Change Control
• Incident Reporting
• Pharmaceutical Manufacturing
• Preventive Maintenance
• Qualification Protocols (IQ/OQ/PQ)
• Regulatory Compliance
• Resident Skills
• Current Good Manufacturing Practices (cGMPS)
• Quality Management Systems
• Data Analysis
• Good Documentation Practices
• Lean Methodologies
• Behavioural Skills
• Detail-oriented with compliance and regulatory alignment mindset

Preferred experience and additional strengths

• Exposure: greenfield and brownfield plant setup activities is preferred
• Exposure: audit response and compliance reporting, ensuring timely closure of gaps is preferred

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 Qualifications vacancy is not an offer for reference REF28709V; 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 REF28709V.

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: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• GMP
• audit
• compliance
• data analysis
• electrical engineering
• mechanical engineering
• manufacturing
• Lean
• maintenance