Job opportunity for Cell and Gene Therapy – QC at Aurigene- Apply before 15th June 2024

Aurigene

Website Aurigene

About Aurigene

Aurigene, a subsidiary of Dr. Reddy’s Laboratories Ltd., is a development-stage biotechnology company dedicated to discovering and clinically developing innovative therapies for cancer and inflammatory diseases. The company’s research and development efforts are concentrated on three primary areas:

  1. Precision Oncology: Developing targeted therapies that precisely attack cancer cells based on their genetic and molecular profiles.
  2. Oral Immune Checkpoint Inhibitors: Creating oral medications that help the immune system recognize and fight cancer by inhibiting checkpoint proteins that often prevent immune cells from attacking cancer cells.
  3. Th-17 Pathway: Investigating treatments that modulate the Th-17 pathway, which plays a crucial role in inflammatory and autoimmune diseases.

Aurigene aims to advance novel and best-in-class therapies through its focused approach in these areas, contributing to the broader efforts of Dr. Reddy’s Laboratories in delivering cutting-edge medical treatments.

Cell and Gene Therapy – QC (Molecular Biology)

Experience: 1-7 years in Flow Cytometry, GMP, qPCR

Job Location: Bangalore

Key Responsibilities

  • Biological and Quality Control Studies: Oversee studies involving established human cancer cell lines, normal human cells, and patient-derived primary cells (including blood, plasma, serum, and PBMC). Ensure all practices follow ethical guidelines and QMS standards compliant with GMP regulations.
  • Cell-Based and Molecular Biology Testing: Perform cell-based and molecular tests integral to cell therapy manufacturing and in-process quality control for viral vectors and final products.
  • Quality Control Screening: Develop and meticulously conduct various QC screening techniques such as DNA/RNA isolation, PCR, qPCR, Flow Cytometry, ELISA, and other quality testing methods in line with established guidelines and criteria, maintaining the highest quality standards.
  • Documentation and Review: Create, review, and maintain SOPs, protocols, and reports to meet program requirements.
  • Communication: Maintain excellent communication skills to effectively interface with internal departments, supporting the workflow of various study-related activities.
  • Coordination: Collaborate with manufacturing, quality assurance, and supply chain teams, ensuring strict adherence to project timelines while maintaining integrity, accuracy, safety, and quality.
  • Compliance and Regulatory: Prepare for and participate in compliance monitoring inspections and interactions with regulatory agencies.

Send your resume to: ashmita_c@aurigene.com
Last Date to Apply: 15th June 2024

Cell and Gene Therapy – QC (Molecular Biology)

Experience: 1-7 years in Flow Cytometry, GMP, qPCR

Job Location: Bangalore

Key Responsibilities

  • Biological and Quality Control Studies: Oversee studies involving established human cancer cell lines, normal human cells, and patient-derived primary cells (including blood, plasma, serum, and PBMC). Ensure all practices follow ethical guidelines and QMS standards compliant with GMP regulations.
  • Cell-Based and Molecular Biology Testing: Perform cell-based and molecular tests integral to cell therapy manufacturing and in-process quality control for viral vectors and final products.
  • Quality Control Screening: Develop and meticulously conduct various QC screening techniques such as DNA/RNA isolation, PCR, qPCR, Flow Cytometry, ELISA, and other quality testing methods in line with established guidelines and criteria, maintaining the highest quality standards.
  • Documentation and Review: Create, review, and maintain SOPs, protocols, and reports to meet program requirements.
  • Communication: Maintain excellent communication skills to effectively interface with internal departments, supporting the workflow of various study-related activities.
  • Coordination: Collaborate with manufacturing, quality assurance, and supply chain teams, ensuring strict adherence to project timelines while maintaining integrity, accuracy, safety, and quality.
  • Compliance and Regulatory: Prepare for and participate in compliance monitoring inspections and interactions with regulatory agencies.

Send your resume to: ashmita_c@aurigene.com
Last Date to Apply: 15th June 2024

To apply for this job email your details to ashmita_c@aurigene.com