Novartis looking for Analytical R&D Scientist - M.Pharm, MSc Apply

Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post : Scientist - Analytical R&D

Job Description
1. Provide analytical and technical support to PHAD/project team at various stages of product development (eg. CSF, FMI and LCM)
2. Design and author analytical documents (e.g., Analytical methods, Stability protocols/reports, Excipient compatibility (EC) protocol/reports; APS protocols/reports, etc.).
3. Support Analytical project leader for setting analytical development strategy.
4. Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.
5. Responsible for project related sample handling (e.g., sampling plans, issuance, storage, distribution, reconciliation/destruction of the samples).
6. Support planning for assigned project activities. Accountable to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned project activities.
7. Provide requests for lab activities to the associates and stakeholders.
8. Manage project activities including logistics at third parties and external testing laboratories.
9. Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).
10. Single point of contact for PHAD/project team and other stakeholders (e.g, BioPharm, Material science and CPP, etc.) for project execution activities.

11. Support internal and external audits and ensure no critical findings within the assigned projects.
12. Actively contribute to team goals.
13. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines.
14. Subway: Author (EC/APS protocol and reports), review of test methods and compatibility study plan.
15. ESOPS: Read SOP access and Review of SOPs.

Candidate Profile
• Desirable knowledge of site language. Up to 10 years (for M.Pharm./M.Sc.) & minimum of 4 years (for Ph.D.) of relevant experience in testing of Solid oral dosage form.
• Good presentation skills and scientific/technical writing skills.
• Good communication skills

Skills
• Dissolution method development
• Titration
• Stability studies
• LC method development
• DVS
• Forced degradation
• Excipient compatibility

Additional Information
Job ID : REQ-10034766
Location : Hyderabad
Industry Type : Pharma / Healthcare / Clinical research
Division : Development
Business Unit : Innovative Medicines
End Date : 20th February 2025