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Dr. Reddy's Laboratories

4 years

ND

Andhra Pradesh

B.Pharm. / Post-Graduation / Life Sciences.

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Location: Pydibimavaram, Andhra Pradesh
Industry Type: Pharma / Healthcare / Clinical Research
Functional Area: Quality Assurance
Experience: 4 years
Qualification: B.Pharm. or Post-Graduation in Life Sciences
Application Deadline: 25th November 2024

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is a leading Indian multinational pharmaceutical company based in Hyderabad, Telangana. Founded by Kallam Anji Reddy, the company is committed to providing affordable and innovative medicines to the global community.

Job Description

We are looking for a dedicated individual to join our Quality Assurance team. The primary responsibility of this role is to ensure compliance with regulatory standards and maintain product quality throughout manufacturing processes. You will be involved in real-time investigations, batch manufacturing oversight, and adherence to global quality standards.

Key Responsibilities

  • In-Process Activities: Execute and assign in-process activities, conduct line clearances, verify materials, and oversee machine startups and sampling activities.
  • Documentation: Review and manage batch records and logbooks, ensuring proper documentation of QA activities.
  • Quality Compliance: Monitor adherence to Good Manufacturing Practices (GMP) and Quality Management System (QMS) elements, addressing any deviations.
  • Investigations: Support supervisors in investigating complaints, batch failures, and Out-of-Specification (OOS) results, and document Corrective and Preventive Actions (CAPA).
  • Cross-Functional Coordination: Collaborate with various teams to drive investigation processes and verify the implementation of CAPA.
  • Audit Support: Assist in internal and external audits, providing necessary documentation and maintaining accurate records.

Candidate Profile

  • Education: B.Pharm. or Post-Graduation in Life Sciences.
  • Experience: Minimum 4 years in Quality Assurance, specifically in IPQA.
  • Knowledge: Strong understanding of Quality Systems, cGMP regulatory requirements (FDA, EU, Indian regulations), and the bio-pharma market.
  • Skills:
    • Excellent communication and influencing skills.
    • Analytical and logical thinking abilities.
    • Self-motivated with a proactive approach.
    • Adaptable and a strong team player.
  • Commitment: Demonstrated commitment to continuous learning and professional development.

Why Join Us?

At Dr. Reddy’s, you will be part of a dynamic team committed to ensuring the highest quality in pharmaceutical manufacturing. We offer a collaborative work environment that fosters growth and innovation.

Application Link