Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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