At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering
an setting 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 team-oriented 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 current 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.
Travel Estimate
NA
Job Requirements
Educational Qualification
M.Sc. in Analytical Chemistry / Organic Chemistry / Pharmaceutical Chemistry/ M.
Pharm (Pharmaceutics) preferred
Experience
Tenure: 2 - 5 Yrs.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities We provide
robust benefits and opportunities to foster personal and professional growth.
Join us at Sun Pharma, where every day is an opportunity to grow, collaborate,
and make a lasting
📌 Executive Analytical Development Vadodara (India)
🏢 Sun Pharmaceutical Industries
📍 India
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