Research Associate II – Analytical Lab
Company: Vantive
Location: Whitefield, Bangalore, India
Department: Research and Development (R&D)
Job Category: Analytical Laboratory / R&D
Req ID: JR-190211
Date Posted: November 10, 2025
Shift: General
Employment Type: Full-time
About Vantive
Vantive is a global leader in vital organ therapy, dedicated to improving and extending the lives of patients through innovative healthcare solutions.
With over 70 years of leadership in kidney care, Vantive continues to evolve by integrating digital solutions, advanced therapies, and service innovation—enhancing both patient experiences and clinical outcomes.
At Vantive, every team member contributes to shaping the future of organ therapy. The organization values courage, excellence, and compassion, providing meaningful career opportunities to those who share its mission to extend lives and expand possibilities.
Position Summary
The Research Associate II – Analytical Lab will be responsible for designing, developing, validating, and executing analytical methods in support of R&D projects, including stability studies, verification, and method transfers.
The role requires a technically skilled, self-motivated professional who can work both independently and collaboratively, demonstrating strong analytical, scientific, and problem-solving capabilities.
Key Responsibilities
1. Analytical Method Development & Validation
Conduct validation, verification, transfer, and stability studies for R&D products.
Independently develop, evaluate, and validate analytical methods as per regulatory requirements.
Design studies and prepare protocols, reports, and procedures with minimal supervision.
Propose appropriate analytical techniques to meet the Analytical Target Profile (ATP).
Investigate and resolve method failures or deviations through scientific analysis.
2. Laboratory Operations & Compliance
Perform laboratory testing in compliance with GxP, ALCOA+, and data integrity standards.
Handle sample receipt, testing, and data entry in LIMS (Laboratory Information Management System).
Manage OOS/OOT investigations, nonconformances, and CAPA implementation.
Ensure Right First Time (RFT) testing and accurate data documentation.
Maintain laboratory equipment and ensure adherence to health and safety standards.
3. Scientific Collaboration & Technical Support
Collaborate with Quality, Regulatory, Operations, and Manufacturing teams to support R&D goals.
Provide technical expertise during cross-functional and global team interactions.
Support preparation of responses to regulatory authority queries related to analytical methods.
Participate in technical review meetings and contribute data-driven insights for decision-making.
4. Continuous Improvement & Innovation
Evaluate existing methods and introduce new technologies or approaches to improve quality, efficiency, and cycle time.
Identify and mitigate project risks, ensuring timely completion of project milestones.
Demonstrate scientific reasoning in proposing process or technology improvements.
5. Documentation & Ownership
Author and own SOPs relevant to analytical techniques and processes.
Maintain accurate test records, logs, and calibration documentation.
Ensure documentation is compliant with cGMP/cGLP standards.
Required Qualifications
Education
Bachelor’s degree in Analytical Chemistry, Pharmaceutical Chemistry, or a related scientific discipline with 8–14 years of experience,
OR
Master’s degree in the same field with 5–10 years of experience.
Technical Skills
Proficiency in analytical techniques, including:
HPLC / UPLC
GC (Gas Chromatography)
AAS (Atomic Absorption Spectroscopy)
Titrations and other wet chemistry techniques
Experience with Empower, Chromeleon, and LIMS software.
Knowledge of GxP regulations, method validation, and stability guidelines.
Strong data analysis, interpretation, and documentation skills.
Familiarity with Microsoft Office tools (Word, Excel, PowerPoint).
Soft Skills
Strong critical thinking and problem-solving abilities.
Excellent written and verbal communication skills.
Strong organizational and time-management capabilities.
Self-driven, proactive, and adaptable to shifting project priorities.
Team-oriented and capable of cross-functional collaboration.
Regulatory & Compliance
Maintain awareness of Quality System Regulations (QSR) and relevant global regulatory guidelines.
Ensure all research, documentation, and reporting activities comply with applicable standards.
Reasonable Accommodation
Vantive is committed to supporting individuals with disabilities. If you require a reasonable accommodation during the application or interview process, please contact the company through the provided [accommodation request form].
Recruitment Fraud Notice
Vantive has identified incidents of fraudulent job offers. Candidates are advised to verify the legitimacy of communications from official Vantive recruitment channels only. Review the company’s official Recruitment Fraud Notice for more information.
Join Vantive
At Vantive, you’ll work on cutting-edge R&D projects that directly impact patients’ lives while growing in a supportive, innovation-driven culture.
If you are passionate about scientific discovery, compliance, and improving patient outcomes — apply now and be part of the future of organ therapy.
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