At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Job Description
- Develop and optimize analytical methods for APIs and drug products (tablets, capsules, granules, suspensions etc).
- Establish methods for assay, dissolution, related substances, degradation products, and content uniformity.
- Perform forced degradation studies to establish stability-indicating methods.
- Execute method validation as per ICH Q2(R1) guidelines.
- Prepare validation protocols and reports.
- Perform impurity profiling and method development for new products.
- Support formulation team with analytical inputs during product development.
- Operate and troubleshoot instruments such as:
- HPLC / UPLC
- Dissolution apparatus
- UV-Visible Spectrophotometer
- GC (if applicable)
- Instrument calibration and compliance.
- Work with formulation development, QA, regulatory affairs, and stability teams.
