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R&D Project Leader Ii – Lsi

10+ years
₹22 LPA – ₹30 LPA
10 June 12, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ B.Tech/ M.Tech/ BE/ ME 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

R&D Project Leader II – Lead System Integrator (LSI) | Vantive | Bengaluru, Karnataka
Req #: JR-168992
Employment Type: Full-time
Department: Research and Development
Posted On: 04/10/2025

About Vantive:
Vantive is a globally recognized leader in vital organ therapy, built on a 70-year legacy in kidney care. We are committed to transforming lives through digital solutions and advanced services in dialysis and beyond. As we expand our portfolio across vital organ support therapies, we aim to deliver flexible treatment options and better outcomes for patients. Vantive offers an inclusive, purpose-driven work environment where innovation thrives and every role contributes to elevating patient care.


Role Overview:
The R&D Project Leader II – Lead System Integrator (LSI) plays a pivotal role in the Kidney Care R&D – Drug Products and Sciences (DPS) organization. You will lead and manage complex R&D projects across drug products and related sciences such as Sterility Assurance, Analytical Chemistry, Extractables & Leachables, and Toxicology. This role demands strong leadership, cross-functional coordination, and deep project management expertise within a highly regulated healthcare setting.


Key Responsibilities:

  • Lead project management activities across drug product and medical device development projects.

  • Own and drive the creation, execution, and tracking of R&D project schedules in collaboration with subject matter experts.

  • Manage technical risk assessments, status reporting, budgeting, and spend tracking.

  • Integrate cross-functional inputs (Regulatory, Marketing, Quality, etc.) into cohesive project deliverables.

  • Facilitate internal meetings, change control boards, and design reviews; manage follow-ups and action items.

  • Ensure adherence to FDA, ISO, and IEC design control regulations and standards.

  • Support parallel projects, identifying interdependencies, and proactively managing conflicts or synergies.

  • Oversee external vendor collaborations including purchase orders and invoice approvals.

  • Maintain and manage internal communication platforms, project documentation, and escalation matrices.


Required Qualifications:

  • Strong understanding of R&D project lifecycles in healthcare/pharma.

  • Proven leadership in coordinating technical inputs into structured project plans.

  • Deep familiarity with FDA, ISO, IEC design controls and regulatory compliance in medical products.

  • Excellent communication skills (written and verbal).

  • Ability to simplify complex problems and lead cross-functional teams to resolution.

  • Highly organized with experience managing multiple concurrent projects.


Education & Experience:

  • Bachelor’s degree in Engineering, Science, or related field.

  • Minimum of 10 years’ experience in R&D or project management roles.

  • Experience within pharmaceutical, medical device, or healthcare sectors preferred.


Salary: ₹22 LPA – ₹30 LPA (estimated based on senior project management roles in medical/pharma industries in India)

Keywords: R&D project leader job, LSI Vantive, medical device project manager Bengaluru, drug products development leadership, Vantive job opening