Live opening · Posted 20 hours ago

Senior Research Associate

OneSource · Bengaluru, Karnataka, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 20 hours ago
CompanyOneSource
LocationBengaluru, Karnataka, India (On-site)
Work modeNo
SourceLinkedin
Listed20 hours ago

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About the role

Description supplied by the original job listing.

Company Description OneSource is a multimodal specialty pharma CDMO offering end-to-end capabilities across diverse technology platforms and therapeutic modalities. With over three decades of experience in specialized drug development and manufacturing, the company provides comprehensive, efficient, and effective solutions to global partners. A team of more than 1,300 professionals, including over 100 techno-commercial experts, collaborates closely with clients to bring their vision to life. OneSource is committed to agility, flexibility, and redefining the CDMO experience, aligning its success directly with that of its partners.
Role Description The Senior Research Associate is a full-time, on-site role based in Doddballapura, Bengaluru. This role involves designing and executing experiments to support drug substance projects, including optimization, and validation across relevant technology platforms. The Senior Research Associate will analyze and interpret data, prepare technical reports, and contribute to documentation needed for regulatory submissions and internal reviews. The position includes close collaboration with cross-functional teams, participation in project meetings, and providing scientific input to ensure project timelines and quality standards are met. The role also involves maintaining laboratory compliance with safety, quality, and GLP/GMP requirements, and mentoring junior team members where appropriate.
Qualifications
Strong foundation in biotechnology, or related disciplines, with a Master’s degree or higher preferred.
Hands-on experience in experimental design, downstream processing and data interpretation within drug development or manufacturing environments.
Knowledge of CDMO operations, regulatory guidelines (e.g., ICH, FDA, EMA), and quality systems such as GLP/GMP.
Proficiency in laboratory instrumentation and relevant software tools for data analysis and documentation.
Effective communication skills for reporting findings, collaborating with cross-functional teams, and interacting with external partners.
Demonstrated ability to manage multiple projects, prioritize tasks, and meet timelines in a fast-paced environment.
Experience mentoring or guiding junior researchers and contributing to a culture of continuous improvement.
Attention to detail, problem-solving mindset, and commitment to safety and ethical research practices.

Work arrangement
No

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