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Sun Pharmaceutical Industries Ltd in Baroda invites an Executive – Analytical Development to join the R&D1 Regulatory Affairs unit. You will ensure cGMP compliance, perform analytical and physiochemical studies for regulatory submissions, calibrate instruments, develop methods, and prepare study protocols and reports.
The role emphasizes training, quality, and safety, with opportunity to contribute to global reference standards and SOP maintenance in a collaborative environment.
Company: Sun Pharmaceutical Industries Ltd
Executive – Analytical Development
R&D1 Regulatory Affairs
G12A
Baroda
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.”
M. Pharm
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)