WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Clinical Sample Management Career at Dr. Reddy’s – Full-time Role

Published on

Dr. Reddy’s Laboratories

0 - 1 Years

₹3.1 Lakhs to ₹5.8 Lakhs per year

Hyderabad, Telangana, India

B.Sc / B.Pharm (Preferred)

Verified Job

Online Application

Why Use Pharmabharat?

Real-Time Job Alerts

Trusted by Top Pharma Employers

Exclusive Pharma Industry Insights

Verified & Trusted Listings

Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company headquartered in Hyderabad, India. With a strong presence in over 66 countries, the company specializes in generic medications, biosimilars, and active pharmaceutical ingredients (APIs). Dr. Reddy’s is known for its innovation-driven approach and commitment to delivering high-quality, affordable healthcare solutions worldwide.

Job Description: Sample Accession Associate

As a Sample Accession Associate at Dr. Reddy’s Laboratories, you will play a crucial role in managing clinical samples, ensuring regulatory compliance, and maintaining laboratory standards.

Key Responsibilities:

1. Sample Management

  • Receive clinical samples from internal and external sources with proper documentation.
  • Verify sample details against records and report discrepancies.
  • Catalog samples in LIMS (Laboratory Information Management System) and store them as per regulatory guidelines.
  • Maintain accurate records of sample receipt, storage conditions, and chain of custody.
  • Monitor inventory control and ensure proper labeling of clinical study samples.
  • Coordinate with lab staff to ensure timely availability of samples for analysis.
  • Dispose of expired or utilized samples following regulatory standards.

2. Management of Sample Accession Area

  • Maintain the sample accession area as per laboratory SOPs (Standard Operating Procedures).
  • Ensure good housekeeping in sample storage facilities.
  • Oversee equipment maintenance, calibration, and validation as per lab standards.
  • Work with maintenance teams to ensure compliance with lab protocols.

3. Reference Standard Management

  • Receive and verify reference standards/drug products from the central warehouse.
  • Maintain proper documentation and assist in material issuance.

4. Compliance & Audit Readiness

  • Adhere to GCP (Good Clinical Practice) guidelines and regulatory requirements.
  • Assist in drafting SOPs as per lab needs.
  • Participate in lab audits and implement CAPA (Corrective and Preventive Actions) for observations.

Qualifications & Skills Required

  • Education: B.Sc / B.Pharm (Preferred)
  • Experience in clinical sample management, LIMS, and regulatory compliance is a plus.
  • Strong attention to detail and documentation skills.
  • Knowledge of GCP, GLP (Good Laboratory Practices), and lab SOPs.

How to Apply?

Application Link

Advertisement ad