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R&D Scientist Validation

3+ years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Education: PhD/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

### **R&D Scientist - Validation | Bangalore, India**  
**Job ID:** R1279524 | **Category:** Science | **Company:** Cytiva (Danaher)  

#### **About Cytiva**  
At **Cytiva**, a **Danaher operating company**, we are dedicated to **advancing human health** by driving innovation in **life sciences, diagnostics, and biotechnology**. Our work supports **biological research, vaccine development, new medicines, and cell & gene therapies** that save lives.  

### **About the Role**  
We are seeking an **R&D Scientist - Validation** to support the **Fast Trak Process Design and Validation Services**. This role involves **planning, executing, and validating R&D projects** related to **new services and product improvements**. You will work across **early-phase development, concept design, testing, and validation** to bring services to market.  

### **Your Responsibilities**  
- Act as a **technical support** for innovation projects, collaborating with **R&D project managers** and cross-functional teams.  
- Assist in defining **technical requirements** for new services and products to meet customer needs.  
- Plan, assess risks, execute, and report on **technical studies** at different project stages.  
- Design and conduct **verification/validation studies** to ensure compliance with **technical and marketing requirements**.  
- Ensure **laboratory compliance** with **Environmental, Health & Safety (EHS) regulations**.  

### **Who You Are**  
#### **Required Qualifications**  
- **Bachelor's, Master's, or PhD** in **Molecular Biology, Biochemistry, Bioengineering, or related fields**.  
- **3+ years** of experience in supporting or leading **technical projects**.  
- Strong **problem-solving skills**, ability to work independently, and handle multiple projects.  
- **Excellent reporting and presentation skills** with the ability to **adapt to different audiences**.  

#### **Preferred Skills**  
- Knowledge of **aseptic laboratory methods and techniques**.  
- Experience with **Good Laboratory Practices (GLP) and scientific methodologies**.  

### **Why Join Us?**  
At **Cytiva**, we offer a **dynamic work environment, competitive benefits**, and the opportunity to **impact the future of science and healthcare**.  

🚀 **Apply now to contribute to cutting-edge R&D validation projects!**