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Senior R&D Scientist Upstream

5+ years
Not Disclosed
10 Feb. 6, 2025
Job Description
Job Type: Full Time Education: M.Sc./B.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

Senior R&D Scientist Upstream – Cytiva (Bangalore, Karnataka, India)

📍 Location: Bangalore, Karnataka, India
📅 Job ID: R1279525

About Cytiva:

At Cytiva, we’re transforming human health by providing innovative solutions for life-saving activities, from fundamental biological research to the development of vaccines, medicines, and cell & gene therapies. As part of Danaher, a global leader in life sciences, we accelerate the discovery, development, and delivery of solutions that safeguard human health. Join us in making a difference, growing your career, and expanding your skills in a company that values learning and improvement every day.

Role Overview:

We are seeking a Senior R&D Scientist Upstream to join the Fast Trak Process Design and Validation Services team. You will be responsible for planning and executing the technical aspects of R&D development or improvement projects within the upstream process development services portfolio. This includes managing early-phase project requirements, designing concepts, conducting testing, and ensuring validation of services/products to meet customer needs.

Key Responsibilities:

  • Serve as a technical lead on innovation projects, collaborating with R&D project managers and other departments to ensure seamless execution of project deliverables.
  • Define technical requirements for new service/product designs to meet customer needs as defined by marketing.
  • Plan, risk-assess, execute, and report on technical studies at various stages of product/service development.
  • Design and conduct verification/validation studies to ensure new products/services meet technical and marketing requirements.
  • Ensure laboratory compliance with Environment, Health & Safety regulations.

Who You Are:

  • Bachelor's, Master’s, or PhD degree in molecular biology, biochemistry, bioengineering, or a related field.
  • 5+ years of experience leading and delivering technical projects.
  • Highly motivated, with a creative and forward-thinking attitude to problem-solving and troubleshooting.
  • Able to work autonomously to achieve results, with the ability to handle multiple projects simultaneously.
  • Strong reporting and presentation skills, able to adjust to different audiences.

Desirable Experience:

  • Aseptic laboratory methods and techniques.
  • Knowledge of Good Laboratory Practice (GLP) and scientific methods.
  • Experience with upstream or downstream biotechnology unit operations.

Why Join Cytiva?

  • Work at the forefront of life-changing science and technology.
  • Collaborate with talented teams to solve complex challenges.
  • Build a career with growth opportunities and continuous learning in the life sciences industry.

🔗 Apply Now: Cytiva Careers