Executive - Analytical Development

SUN PHARMA; Vadodara; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Sun Pharma is seeking an Executive Analytical Development Orals in Vadodara to advance analytical methods for APIs and products. You will contribute to method development, validation, and stability studies, collaborating with cross-functional teams in R&D and regulatory affairs.

The role requires 2–5 years of relevant experience, MSc in Analytical/Pharmaceutical Chemistry or MPharm, and hands-on experience with HPLC/UPLC, dissolution, UV-Vis, and possibly GC.

Qualifications

• MSc in Analytical/Pharmaceutical Chemistry or MPharm preferred.
• Experience in analytical method development and validation.
• Knowledge of ICH guidelines and regulatory requirements.

Responsibilities

• Develop and optimize analytical methods for APIs and dosage forms (tablets, capsules, granules, suspensions).
• Establish assay, dissolution, related substances, degradation products, and content uniformity methods.

Skills

Analytical Chemistry

Problem Solving

Teamwork

Documentation

Education

MSc Analytical Chemistry / Organic Chemistry / Pharmaceutical Chemistry / M.Pharm (Pharmaceutics)

Tools

HPLC/UPLC

Dissolution testing

UV-Visible spectrophotometer

GC

Job description

Job Title

Executive Analytical Development Orals

Business Unit

R&D1 Regulatory Affairs

Job Grade

G12A

Location

Vadodara

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.

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 impact. Let’s create a brighter future together

Disclaimer

The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).