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Biotechnology Job at Syngene Bangalore

Looking to kickstart or grow your career in a high-demand Biotechnology Job? This is an exciting opportunity for life science graduates to join Syngene as a QC Bioassay Analyst in Bangalore. With hands-on exposure to biologics testing, quality control, and advanced lab techniques, this role is perfect for candidates aiming to build a strong foundation in the biotech industry.

About the Company

Syngene International Ltd., incorporated in 1993, is a global discovery, development, and manufacturing organization providing integrated scientific services across pharmaceutical, biotechnology, nutrition, animal health, and specialty chemical industries. The company collaborates with global leaders such as Bristol-Myers Squibb, Amgen, GSK, and Merck KGaA, supported by a large team of scientists driving innovation and R&D excellence.

Job Details:

  • Job Title: QC Bioassay Analyst
  • Location: Bangalore, Karnataka, India (560099)
  • Company: Syngene International Ltd.
  • Department: Quality Control – Biologics
  • Work Location: Biocon Park, Bangalore

Role Overview

The QC Bioassay Analyst is responsible for performing bioanalytical testing in a biologics quality control environment. The role involves handling bioassay techniques, ensuring compliance with laboratory standards, maintaining instrument calibration, and supporting quality and audit readiness activities.

Key Responsibilities

  • Perform plate-based and cell-based bioassay analytical techniques
  • Conduct analysis of in-process and finished product samples in shifts
  • Analyze stability samples as per protocols
  • Handle calibration and maintenance of QC instruments and equipment
  • Ensure completion of assigned training and support team deliverables
  • Follow SOPs/IOPs and adhere to Good Laboratory Practices (GLP)
  • Maintain accurate and error-free documentation
  • Coordinate with external vendors for calibration and preventive maintenance
  • Monitor storage chambers and ensure compliance with temperature requirements
  • Ensure all instruments are in calibrated condition
  • Address equipment breakdowns and coordinate with service providers for timely resolution
  • Maintain audit readiness and support audit preparation activities
  • Track and complete CAPA actions from previous audit observations
  • Support additional tasks assigned by the team lead

Key Functional Responsibilities

  • Work in shifts to ensure timely release of in-process and finished product samples within TAT
  • Ensure compliance with analytical and quality standards
  • Manage calibration activities and coordinate with vendors for equipment maintenance

Educational Qualification

  • Bachelor’s or Master’s degree in Science
  • Master of Technology in Biotechnology / Bioprocess Engineering

Technical & Functional Skills

  • Basic knowledge of biologics manufacturing and testing compliance requirements
  • Understanding of analytical and quality control procedures
  • Good communication skills
  • Ability to collaborate effectively with team leads

Behavioral Competencies

  • Strong focus on task completion
  • Assertive and proactive work approach
  • High personal integrity and positive attitude

Work Environment

  • Laboratory-based role in a biologics QC setting
  • Shift-based operations
  • Compliance-driven and audit-focused environment

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BioTecNika Bureau
BioTecNika Bureau is the official editorial and research desk of BioTecNika, dedicated to bringing reliable updates, career guidance, exam information, job alerts, scholarships, industry trends, and learning resources for life science and biotechnology students, researchers, and professionals. Since 2006, BioTecNika has been committed to simplifying complex scientific information and helping learners make informed academic and career decisions.