Executive - ADD

Sun Pharmaceutical Industries, Inc.; Vadodara; On-site; INR 600,000 - 800,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd. seeks a Senior Executive-Analytical Development to lead analytical method development, validation, transfer and troubleshooting across a range of dosage forms. The role requires hands-on experience with chromatographic and spectroscopic techniques and collaboration with formulation, quality and regulatory teams.

The ideal candidate holds an M. Pharm with 1–5 years of experience and will work within the R&D1 Regulatory Affairs unit at Sun Pharma.

Qualifications

• Experience in analytical method development, validation and transfer.
• Hands-on skills in HPLC/UPLC, GC, UV, FTIR, dissolution and particle size analysis.
• Strong knowledge of ICH/cGMP for sterile and non-oral dosage forms.

Responsibilities

• Develop and validate analytical methods for various dosage forms.
• Transfer methods and troubleshoot analytical issues.
• Collaborate with formulation, quality and regulatory teams.

Skills

Analytical development

HPLC/UPLC

GMP

Regulatory documentation

Team collaboration

Education

M. Pharm

Tools

HPLC/UPLC

GC

UV

FTIR

Dissolution

Particle Size Analysis

Job description

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Company: Sun Pharmaceutical Industries Ltd

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Job Title:

Senior Executive-Analytical Development

Business Unit:

R&D1 Regulatory Affairs

Job Grade

G11B

Location :

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.”

J ob 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.

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Job Requirements

Educational Qualification

M. Pharm

Experience

Tenure 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)