Syngene Pharma Associate Scientist Job Opening - Apply Online
"Discover the Exciting Job Posting in Toxicology at Syngene - Apply Now!"

Syngene Pharma Associate Scientist Job Opening – Apply Online

Associate Scientist (56003)

Requisition ID: 56003

Posted: 05/07/2024

Location: India

Job Description

Job Title: Study Personnel/Study Director – Toxicology

Job Location: Bengaluru

Job Grade: 8-I

About Syngene

Syngene ( is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety on par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit.

Mandatory expectations for all roles as per Syngene safety guidelines

  • Overall adherence to safe practices and procedures for oneself and the aligned teams.
  • Contributing to the development of procedures, practices, and systems that ensure safe operations and compliance with the company’s integrity and quality standards.
  • Promoting a corporate culture that fosters an environment, health, and safety (EHS) mindset and operational discipline in the workplace at all times.
  • Ensuring the safety of oneself and team members by adhering to safety protocols and following EHS requirements in the workplace at all times.
  • Ensuring all mandatory training related to data integrity, health, and safety measures are completed on time by all team members, including oneself.
  • Compliance with Syngene’s quality standards at all times.

Role Accountabilities

  • Prepare study plans considering client and regulatory requirements.
  • Prepare study schedules, communicate with all study personnel, and ensure the proper conduct of the study.
  • Prepare reports after each study is completed, which involves evaluating data output by applying scientific knowledge and skills.
  • Maintain the highest regulatory standards (GLP and AAALAC recommendations) during any activity conducted in the facility by continuously monitoring and checking all instruments/equipment used in a study and conducting activities per SOPs.
  • Prepare and periodically revise SOPs. Prepare and present experimental conduct protocols to the Institutional Animal Ethics Committee.
  • Periodically verify data generated during the study.
  • Archive the study plan, study report, raw data, and related material as per the study plan.
  • Coordinate with Principal Investigators and/or study personnel in case of multi-site studies, keeping them informed of their findings during the study and receiving and evaluating their respective individual reports for inclusion in the final study report.

Syngene Values
All employees will consistently demonstrate alignment with our core values:

  • Excellence
  • Integrity
  • Professionalism

Specific Requirements for This Role


  • 3-6 years

Skills and Capabilities

  • Good understanding and hands-on experience in toxicology.
  • Preferable knowledge of related disciplines, including toxicokinetics, pathology, and analytical chemistry.
  • Ideally, you should be working in or have experience within contract research, but a successful candidate may also have experience within pharmaceutical companies or an academic background related to a toxicology discipline.


  • MSc / MPharma / MVSc

Link to Original Notification to apply

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