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Scientist I, Bangalore

1-3 years
Not Disclosed
10 Jan. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Title: Scientist I - Fast Track Validation & Lab Ops

Company: Cytiva, a Danaher Operating Company
Location: Bengaluru, India
Work Schedule: On-site

About Cytiva:
At Cytiva, we are dedicated to advancing future therapeutics, ranging from fundamental biological research to the development of innovative vaccines, new medicines, and cell and gene therapies. Our work saves lives, and we are united by a shared commitment to innovate for tangible impact. As part of Danaher’s system of continuous improvement, you’ll be instrumental in turning ideas into innovations that matter.

Join a culture of belonging where your unique viewpoint is valued. At Cytiva, you will collaborate with people who care deeply for each other, our customers, and their patients—helping you grow and thrive while making a real difference in the field of life sciences.

Role & Responsibilities:
As a Scientist I, you will play an essential role in supporting the Fast Track Validation & Lab Ops team by performing a variety of testing tasks. You will be responsible for the preparation, execution, and completion of test work with minimal supervision, contributing to key initiatives such as R&D, NPI, NPD, and QC release testing.

Key Responsibilities:

  • Execute basic complexity test work with minimal guidance.
  • Support R&D, NPI, NPD, and QC release testing as required.
  • Review job requests and relevant MSDS, ensuring all requirements are understood and documented in accordance with laboratory SOPs.
  • Prepare and organize data, ensuring compliance with timelines and project management.
  • Operate and troubleshoot laboratory equipment, ensuring test work is completed according to requirements.
  • Document raw data and immediately notify laboratory management of any delays or issues.
  • Prepare laboratory reports that meet the specified requirements, ensuring on-time delivery.

What You Will Do:

  • Develop competence by performing structured work assignments.
  • Apply existing procedures to solve routine or standard problems.
  • Contribute to scientific analysis of data, applying basic knowledge of scientific principles.
  • Ensure proper application of Aseptic laboratory techniques and measurement methods.
  • Familiarize with and apply Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) where necessary.

Who You Are:

  • Skilled in Aseptic laboratory techniques and measurement methods.
  • Ability to perform microbiology test work and execute work instructions.
  • Understanding of GLP and GMP requirements.
  • Strong scientific analysis capabilities, with proficiency in PC-based programs.
  • Bachelor’s or Master’s degree in Microbiology or Life Sciences.

Desired Experience:

  • 1–3 years of relevant industry experience.

Why Join Cytiva?
Cytiva, a Danaher operating company, offers competitive benefits that extend beyond the workplace. Our health care programs, paid time off, and other benefits enrich your life beyond the job.

Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. Join us in our mission to empower life-changing innovations.

Equal Opportunity Employer:
Danaher and Cytiva value diversity and inclusion, celebrating the unique perspectives that come from a diverse workforce. We are committed to providing equal opportunities for all employees, customers, and partners.