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Research Associate Ii

5-10 years
Not Disclosed
10 March 3, 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 II

Location: Bengaluru, Karnataka, India
Job ID: JR-147010
Category: Research and Development
Company: Vantive

About Vantive:

Vantive is a vital organ therapy company committed to extending lives and expanding possibilities for patients and care teams. With 70 years of expertise in kidney care, we continue to drive meaningful innovations, focusing on digital solutions and advanced services. Our goal is to elevate dialysis experiences while expanding beyond kidney care to transform vital organ therapies.

At Vantive, we strive for excellence, encourage courageous thinking, and reject mediocrity. Join our mission to improve patient lives worldwide.

Key Responsibilities:

  • Conduct laboratory testing, including validation, verification, transfer, and stability studies.
  • Design and execute analytical methods and experiments.
  • Develop and document analytical target profiles and testing protocols.
  • Evaluate, validate, and transfer analytical methods while investigating failed acceptance criteria.
  • Ensure compliance with cGxP, Data Integrity, and Quality Culture standards.
  • Perform routine and non-routine R&D testing in a regulated laboratory environment.
  • Utilize HPLC/UPLC, GC, Titrations, AAS, and other analytical techniques.
  • Manage Laboratory Investigations (OOS/OOT) and implement corrective and preventive actions.
  • Maintain and troubleshoot lab equipment, ensuring adherence to health and safety standards.
  • Collaborate with global teams across quality, regulatory, operations, and manufacturing functions.
  • Handle software tools such as Empower, Chromeleon, LIMS, MS Word, and spreadsheets.
  • Prepare regulatory responses and participate in technical review meetings.

Qualifications:

  • Education:
    • Bachelor’s degree with 8-14 years of experience OR
    • Master’s degree with 5-10 years of experience in Analytical Chemistry/Pharmaceutical Chemistry.
  • Skills & Experience:
    • Strong knowledge of regulatory validation & stability guidelines.
    • Expertise in analytical techniques (HPLC/UPLC, GC, AAS, etc.).
    • Ability to analyze data, problem-solve, and adapt to shifting priorities.
    • Effective team collaboration, communication, and technical writing.
    • Understanding of project schedules and ability to contribute beyond assigned scope.

Additional Information:

Vantive is committed to providing reasonable accommodations to individuals with disabilities. Beware of employment scams and refer to our Recruitment Fraud Notice for more details.