Scientist

2 weeks ago

Hyderabad Telangana, India Novartis Full time

Major Accountabilities
- Develop and optimize new dissolution method (Biorelevant and discriminatory dissolution method) mimicking the physiological system
- Independently perform and document solubility experiments, dissolution method activities and other characterization methods (DT, solubility, IDR, Viscosity etc).
- Testing of various developmental formulations in biorelevant and discriminatory dissolution methods
- Analysis of samples using various analytical techniques like HPLC/UPLC and spectrophotometric methods. Addressing the trouble shoots in chromatographic methods
- Write protocols, reports or lab procedures based on templates under expert’s supervision.
- Document Risk assessment at pre-evaluation stage under expert’s guidance.
- Knowledge of PBPK/IVIVC models.
- Assist modeling expert in developing various in-silico tools like Gastroplus/Phoenix WinNonlin etc.
- Work in close collaboration with multifunctional project team

**Commitment to Diversity & Inclusion**:

- We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._

**Minimum requirements**
- Experience of 2-4 years in Analytical development from generic pharmaceutical industry.
- M Pharm (Pharmaceutical Analysis, Pharmaceutics); M Sc (Analytical Chemistry); B Pharm
- Attributes required of the job e.g. the ability to work independently; the ability to work in a team; shows initiative; able to work with all levels of staff.
- Strong written and oral communication skills.

**Division**

SANDOZ

**Business Unit**

Small Molecules STO

**Country**

India

**Work Location**

Hyderabad, AP

**Company/Legal Entity**

Sdz Pvt Ind

**Functional Area**

Research & Development

**Job Type**

Full Time

**Employment Type**

Regular

**Shift Work**

No

**Early Talent**

No

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