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Research Scientist I

Vantive
Vantive
7-14 years
₹14 – ₹22 LPA
10 July 29, 2025
Job Description
Job Type: Full Time Education: PhD/MS/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 Scientist I
Location: Whitefield, Bengaluru, India
Job ID: JR - 179360
Job Type: Full-time
Department: Research and Development
Date Posted: July 22, 2025
Estimated Salary: ₹14 – ₹22 LPA (based on education and experience level)


About Vantive:
Vantive is a pioneering vital organ therapy company dedicated to advancing care and extending lives. With 70 years of legacy in kidney care, we are driving innovation in dialysis, drug-device combinations, and vital organ therapies using cutting-edge science, digital solutions, and customer-centric strategies. At Vantive, you’ll find purposeful work and collaborative teams committed to transforming patient health.


Your Role at Vantive:
As a Research Scientist I in the Analytical Chemistry and Stability (ACS) team, you will provide technical leadership in trace level elemental analysis for medical devices and drug products. This includes hands-on method development using ICP-OES, ICP-MS, and AA techniques. Your work will support regulatory compliance, risk assessment, and change control initiatives for both new and marketed products within the Renal and Acute Care business.


Key Responsibilities:

  • Elemental Analysis & Methodology:

    • Lead elemental impurity projects using ICP-OES, ICP-MS, and AA.

    • Convert legacy AA methods to ICP-based methods and prove equivalency statistically.

    • Develop, validate, and execute methods for trace level elemental detection in compliance with global regulatory expectations.

  • Regulatory & Risk Assessments:

    • Write impact assessments, gap analysis, technical rationales for elemental impurities.

    • Maintain current knowledge of ISO, ICH, and FDA requirements for elemental analysis.

  • Cross-functional Collaboration:

    • Collaborate with regulatory, toxicology, materials science, preclinical, and design teams to develop comprehensive testing and characterization strategies.

    • Serve as study director for multiple analytical chemistry projects.

  • Compliance & Documentation:

    • Ensure proper documentation in alignment with GMP standards and internal Quality Systems.

    • Lead change control assessments related to elemental impurities in manufacturing environments.


Qualifications:

  • Education:

    • Bachelor’s degree in Analytical or Organic Chemistry with 14+ years of relevant experience

    • OR Master’s degree with 7+ years

    • OR Ph.D. with 3+ years of direct hands-on experience.

  • Technical Skills & Experience:

    • Deep experience with ICP-MS, ICP-OES, AA techniques

    • Demonstrated experience in GMP and regulatory environments

    • Proven history of working in global, cross-functional project teams

    • Proficient in technical writing and regulatory documentation

  • Soft Skills:

    • Independent problem-solver and critical thinker

    • Strong communication and cross-functional collaboration skills

    • Strategic mindset with hands-on execution abilities


Why Join Vantive?

  • Work on cutting-edge therapies that impact patient lives.

  • Collaborate with top scientists and global experts in analytical chemistry.

  • Thrive in a mission-driven environment that values courage, innovation, and scientific excellence.

  • Be part of a legacy company leading the transformation of vital organ care.