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Dr. Reddy's Laboratories

Global generic medicines and APIs exporter

Team Member - Quality Control

Inspection & TestPosted on Nov 11
Full-timeHyderabad, Telangana, IndiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Chemistry, Analytical Chemistry, or a related field is required.
  • Requires 2 to 5 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry.
  • Proficient in analytical techniques, including sampling and analysis of packaging and raw material samples.
  • Experienced in operating and maintaining analytical instruments according to standard operating procedures.
  • Competent in SAP activities related to sample tracking, documentation, and data entry.
  • Knowledgeable about cGMP, SOPs, and STPs, and able to maintain accurate documentation and adhere to specifications.
  • Able to follow safety precautions and procedures during analysis, including laboratory safety, Job Safety Analysis, and proper use of Personal Protective Equipment.
  • Experienced in handling and maintaining the chemical and solvent store, including preparing and maintaining volumetric solutions and reagents.
  • Able to communicate and collaborate with the Group Leader, report discrepancies and incidents, and provide timely updates.
  • Able to take initiative in proper instrument use and care, timely sample destruction, and other assigned responsibilities.
  • Able to address discrepancies and incidents and support smooth laboratory operations.
  • Must uphold ethical standards, comply with SOPs, and follow regulatory requirements.

Responsibilities

  • Ensure compliance with cGLP and safety requirements in the assigned area and maintain 5S in the laboratory.
  • Perform authorized SAP and LIMS transactions, including authorized SAP transactions and document approvals in LIMS.
  • Prepare method transfer protocols and reports.
  • Ensure SOP compliance in the laboratory and follow relevant SOPs and STPs during analysis.
  • Analyze raw material, in-process, finished-product, stability, and nitrosamines samples; perform method validation, method transfers, and method verification.
  • Follow online documentation and calculation practices.
  • Verify analytical results against specification limits.
  • Prepare and execute instrument methods and processing methods.
  • Prepare, review, and process sample sets, including audit-trail review.
  • Manage Empower3 software and review audit trails.
  • Complete required training within established timelines.
  • Initiate and investigate out-of-specification (OOS) events, incidents, and quality notifications.
  • Ensure compliance with regulatory and country-specific queries.
  • Verify export certificates of analysis (COAs) and technical pack documents.
  • Analyze method-related issues.
  • Prepare and maintain laboratory analytical standards.
  • Calibrate instruments and verify their performance.
  • Coordinate laboratory SOP preparation and training.
  • Carry out additional responsibilities assigned by the Group Leader.

Desired Qualifications

  • Experience in the pharmaceutical or a related industry is preferred.

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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