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Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Qualification & Validation Specialist

Validation, Compliance & Quality SystemsPosted on Nov 14
Full-timeVisakhapatnam, Andhra Pradesh, IndiaNo salary listedIn-person

About the Job

Requirements

  • A graduation qualification in Pharmacy, Science, Mechanical Engineering, Chemical Engineering, Industrial Engineering, Electrical Engineering, Biotechnology, or a related field is mandatory.
  • At least 8 years of experience is required.
  • Functional skills include calibration, change control, incident reporting, pharmaceutical manufacturing, preventive maintenance, qualification protocols (IQ/OQ/PQ), and regulatory compliance.
  • Knowledge of current Good Manufacturing Practices (cGMP), quality management systems, data analysis, good documentation practices, and lean methodologies is required.
  • Experience qualifying pharmaceutical equipment, clean utilities, and process equipment, with a basic understanding of computer system validation, is desired.
  • Experience with risk assessments and ensuring traceability, documentation integrity, and validation processes is desired.
  • Exposure to greenfield and brownfield plant setup activities is preferred.
  • Exposure to audit response and compliance reporting, including timely closure of gaps, is preferred.

Responsibilities

  • Execute qualification protocols (IQ, OQ, and PQ), coordinating with vendors and cross-functional teams.
  • Compile qualification documents and prepare risk assessments, standard operating procedures (SOPs), validation programs, and master plans.
  • Execute equipment requalification according to schedule and update qualification schedules.
  • Assist with audit responses and coordinate with Quality Assurance (QA) on corrective and preventive actions (CAPA), incidents, deviations, and audit reports.
  • Prepare master documents, including SOPs, operating instructions, and validation master plans (VMPs), and coordinate risk assessments for equipment and systems.
  • Assess safety risks, drive implementation of safe procedures, and create awareness among team members.
  • Support digital system implementation (eVal) and coordinate user requirement specifications (URS), design qualification (DQ), and quantitative risk assessments with production and engineering.
  • Coordinate with QA and engineering on cGMP document approvals and vendor audits.

Desired Qualifications

  • Experience qualifying pharmaceutical equipment, clean utilities, and process equipment, with a basic understanding of computer system validation.
  • Experience with risk assessments and ensuring traceability, documentation integrity, and validation processes.
  • Exposure to greenfield and brownfield plant setup activities.
  • Exposure to audit response and compliance reporting, including timely closure of gaps.

About the Company

Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Dr. Reddy's Laboratories focuses on affordable generic medicines and pharmaceutical ingredients. Its products include generic drugs and active pharmaceutical ingredients (APIs) produced in-house and distributed worldwide. The company grew from a Hyderabad-based startup in 1984, becoming the first Indian firm to export APIs to Europe in 1986 and to enter the U.S. market in the early 1990s, culminating in a 2001 NYSE listing that underscored its global standards. Today, the group operates in over 150 countries, supported by ongoing research and development to create new and improved medications. The core goal is to improve global health by providing high-quality, affordable healthcare solutions at scale.

Company size
10,001+
Company stage
IPO
Headquarters
Hyderabad, India
Founded
1984

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