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Research Associate-Iii

8-14 years
₹14 LPA – ₹20 LPA
10 June 12, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Associate III – Testing Coordinator | Vantive | Bengaluru, Karnataka
Req #: JR-171047
Employment Type: Full-time
Department: Research and Development
Posted On: 05/05/2025

About Vantive:
Vantive is a global leader in vital organ therapy, rooted in 70 years of innovation in kidney care. As a newly independent company emerging from Baxter, Vantive is focused on elevating patient outcomes through advanced therapy delivery, digital health solutions, and next-gen dialysis systems. Join a team that is passionate, bold, and committed to driving meaningful improvements in global healthcare.


Position Summary:
As Research Associate III – Testing Coordinator, you will lead analytical and stability testing operations with a focus on planning, coordination, and lab operational excellence. This position requires cross-functional collaboration with global teams and stakeholders to ensure testing timelines, compliance, and project success across various analytical and stability platforms.


Key Responsibilities:

  • Manage testing schedules and ensure on-time execution of analytical and stability testing activities.

  • Coordinate with analytical teams, CROs, global stakeholders, and other labs (Particle, Sterility/BET, etc.).

  • Lead internal operational excellence initiatives and contribute to process improvement.

  • Anticipate business needs and proactively align testing activities with project timelines and deliverables.

  • Ensure regulatory compliance in laboratory operations as per QSR, GxP, and other standards.

  • Maintain laboratory sample inventory and coordinate import licenses and chemical procurement.

  • Supervise and resolve analytical equipment issues in collaboration with technical teams.

  • Handle laboratory deviations, atypical/OOS/OOT results, and lead scientific investigations with appropriate CAPA.

  • Track and forecast resource allocations and inventory with efficiency.

  • Author and follow SOPs and relevant procedural documentation.

  • Use tools like TrackWise and MS Office for documentation, tracking, and reporting.


Candidate Profile:

  • Education: Master’s degree in Chemistry or Pharmaceutical Sciences with 5–10 years of experience; OR Bachelor’s degree with 8–14 years in a relevant domain.

  • Experience:

    • Stability testing, analytical method validation/transfer, lab operations, and regulatory documentation.

    • Familiarity with global regulatory standards (QSR, GxP).

    • Resource and inventory planning, problem-solving, and risk management.

    • Working with analytical software and tools (e.g., TrackWise).

    • Managing cross-functional teams and collaborating with global counterparts.

  • Skills:

    • Strong leadership, planning, and communication abilities.

    • Ability to multitask across several timelines and project phases.

    • Scientific acumen and decision-making based on critical thinking.

    • Proficient with Excel, Word, PowerPoint, and other business tools.


Salary: ₹14 LPA – ₹20 LPA (estimated based on senior coordinator roles in analytical testing & lab operations in India)