Research Assistant I (In Vivo)

Company Description
APT Testing and Research Pvt. Ltd. (APTRPL) is an established research and testing organization with over three decades of experience supporting the pharmaceutical, biotechnology, medical device, chemical, and allied industries.
APTRPL combines extensive regulatory and industry experience with evolving scientific expertise and modern technologies. Our capabilities include regulatory and safety testing, in vivo and in vitro research, customized R&D, bioassays, and specialized scientific services.
As a NABL-accredited and Maharashtra FDA-approved laboratory, APTRPL is committed to scientific rigor, quality, regulatory compliance, and the continued expansion of its technical capabilities to support the evolving needs of its partners.
Role Description
The Research Assistant I – In Vivo is a full-time, on-site position based in Pune.
The role involves supporting the conduct and documentation of in vivo research studies in accordance with approved study plans, standard operating procedures, and applicable ethical and regulatory requirements.
Key responsibilities include monitoring and handling laboratory animals, performing assigned dosing and biological sample collection procedures, recording study observations, and maintaining complete and accurate study documentation.
The Research Assistant I will also assist with the preparation of study plans and test reports, maintain relevant equipment and calibration records, and work closely with scientists and technical staff to ensure study activities are completed accurately and according to defined timelines.
This position provides hands-on exposure to regulated in vivo research and an opportunity to develop practical skills across study execution, documentation, and laboratory operations.
Key Responsibilities
• Support the conduct of in vivo studies according to approved study plans, SOPs, and defined study schedules.
• Handle and monitor laboratory animals and accurately document study observations.
• Perform assigned dosing and test-item administration procedures using approved methods.
• Conduct biological sample and biofluid collection as required by individual studies.
• Maintain accurate and contemporaneous records of study activities, observations, dosing, and sample collection.
• Assist in the preparation and maintenance of study plans and associated study documentation.
• Support the compilation of study information and preparation of test reports.
• Maintain equipment-related records, including applicable calibration documentation.
• Follow laboratory quality, safety, ethical, and regulatory requirements.
• Coordinate with scientists and technical team members to support timely and accurate completion of study activities.
Qualifications
• Bachelor’s degree in Life Sciences, Pharmacology, Biotechnology, Veterinary Science, Zoology, or a related discipline.
• Familiarity with laboratory animal handling and in vivo research procedures is preferred.
• Understanding of biological sample collection and routine laboratory techniques is an advantage.
• Basic knowledge of GLP principles, SOP-driven laboratory work, and ethical requirements for animal research is preferred.
• Strong attention to detail and ability to maintain accurate scientific and study documentation.
• Ability to follow study protocols, SOPs, and defined procedures consistently.
• Good organizational and communication skills.
• Ability to work effectively as part of a scientific and technical team.
• Willingness to learn and develop practical skills within a structured, quality-focused research environment.

Work arrangement
No