Executive - ADD

SUN PHARMA; Vadodara; On-site; INR 600,000 - 1,200,000; Full time

Job summary

Sun Pharma in Vadodara invites applications for Senior Executive-Analytical Development. The role focuses on method development, validation, transfer, and troubleshooting across sterile and non-oral dosage forms, using HPLC/UPLC, GC, UV, FTIR, and dissolution techniques.

The ideal candidate holds an M. Pharm and 1–5 years of hands-on experience, with strong knowledge of ICH guidelines and cGMP, collaborating with formulation, quality, and regulatory teams to support product development.

Qualifications

• M. Pharm is required.
• 1–5 years of experience in analytical development.
• Hands-on experience with chromatographic and spectroscopic techniques.
• Strong understanding of ICH guidelines and cGMP.

Responsibilities

• Develop, validate, transfer analytical methods for a wide range of dosage forms.
• Troubleshoot analytical issues and support lifecycle management.
• Collaborate with formulation, quality, and regulatory teams to ensure regulatory compliance.

Skills

Analytical Development

ICH Guidelines

cGMP

Regulatory Documentation

Data Analysis

Education

M. Pharm

Tools

HPLC/UPLC

GC

UV

FTIR

Dissolution

Particle Size Analysis

Job description

Job Description:

.

Job Title: Senior Executive-Analytical Development

Business Unit: R&D1 Regulatory Affairs

Job Grade: G11B

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 others' journeys.

Job Description

The Analytical Scientist will be responsible for analytical method development, validation, transfer, and troubleshooting for a wide range of pharmaceutical dosage forms, including injectables, liposomal formulations, microspheres, inhalation products, topical formulations, and conventional oral dosage forms. The role requires hands-on expertise in chromatographic and spectroscopic techniques (HPLC/UPLC, GC, UV, FTIR, dissolution, and particle size analysis), characterization of complex drug delivery systems, stability studies, and regulatory documentation. The candidate should possess a strong understanding of ICH guidelines, cGMP requirements, and analytical challenges associated with sterile and non-oral dosage forms, while collaborating closely with formulation, quality, and regulatory teams to support product development and lifecycle management.

Travel Estimate: NA

Job Requirements:

Educational Qualification: M. Pharm

Experience: 1- 5 years of experience.

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)