Regulatory Affairs Specialist

Company Description

Krosyl Pharmaceuticals Pvt. Ltd. is a leading emerging pharmaceutical company, committed professionally and ethically to providing efficient and affordable healthcare. Our state-of-the-art infrastructure and quality procedures ensure the production of high-quality products at affordable prices. Krosyl Pharmaceuticals is ISO 9001:2015 and WHO-GMP certified, dedicated to maintaining the highest standards in the industry.

Role Description

This is a full-time, on-site role for a Regulatory Affairs Specialist, located in Vadodara. The Regulatory Affairs Specialist will be responsible for handling regulatory documentation, ensuring compliance with regulatory requirements, and managing regulatory submissions. The specialist will also be involved in coordinating with different departments to ensure adherence to regulatory affairs and standards.

Qualifications

• Regulatory Documentation, Regulatory Compliance, Regulatory Requirements skills
• Experience in Regulatory Affairs and managing Regulatory Submissions
• Attention to detail and strong organizational skills
• Effective communication and interpersonal skills
• Ability to work in a fast-paced environment and meet tight deadlines
• Experience in the pharmaceutical industry is preferred
• Bachelor’s degree in Pharmacy, Life Sciences, or a related field