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R&D Scientist Validation

3+ years
Not Disclosed
10 Feb. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/PhD 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 Scientist Validation – Cytiva

📍 Location: Bangalore, Karnataka, India
📅 Job Id: R1279524
📂 Category: Science

About Cytiva:

Cytiva, part of Danaher Corporation, is a global leader in life sciences, diagnostics, and biotechnology. The work we do at Cytiva saves lives, and we are united by a shared commitment to innovate for tangible impact. Our teams accelerate human health breakthroughs, from life-saving biological research to creating innovative medicines and therapies. Cytiva offers a thriving culture of belonging where every unique viewpoint matters.

Role Overview:

We are looking for a R&D Scientist - Validation to join our Fast Trak Process Design and Validation Services team. This role will be responsible for supporting planning and executing the technical aspects of R&D development and improvement projects related to validation services. You’ll work on all phases, from early specification definition to design, testing, and validation.

Key Responsibilities:

  • Support innovation projects, ensuring the seamless execution of deliverables.
  • Collaborate with R&D project managers and departments to meet customer-defined marketing needs.
  • Define technical requirements for new service/product designs.
  • Plan, assess risks, execute, and report on technical studies at various stages.
  • Design and conduct verification/validation studies to demonstrate compliance with technical and marketing requirements.
  • Ensure laboratory compliance with Environment, Health & Safety regulations.

Qualifications & Requirements:

  • Education: Bachelor's, Master's, or PhD degree in molecular biology, biochemistry, bioengineering, or related fields.
  • Experience: Minimum 3+ years of strong experience supporting or leading technical projects.
  • Skills:
    • Highly motivated, with a creative and problem-solving attitude.
    • Ability to work autonomously and manage multiple projects simultaneously.
    • Strong reporting and presentation skills, adaptable to various audiences.

Preferred Experience (a plus):

  • Aseptic laboratory methods and techniques.
  • Knowledge of Good Laboratory Practice (GLP) and scientific methods.

Why Cytiva?

  • Join a dynamic team committed to accelerating impactful life sciences innovations.
  • Opportunity to work on projects that transform human health.
  • Cytiva offers a culture that encourages continuous growth and improvement, with opportunities to make a real difference.

🔗 Apply Now: Cytiva Careers