Regulatory Affairs Associate

The Regulatory Affairs Executive is responsible for ensuring compliance with regulatory requirements for pharmaceutical products. Your primary role will involve preparing and submitting regulatory documentation, coordinating with internal teams, and staying informed about industry regulations. You will play a crucial part in ensuring product approvals and renewals, liaising with regulatory authorities, and reviewing product labeling to maintain regulatory compliance. Additionally, you will collaborate with cross-functional teams for data collection, maintain regulatory files, monitor regulatory guideline changes, and assist in audits and inspections by regulatory agencies. To qualify for this role, you should have a Bachelor's degree in Pharmacy, Life Sciences, or a related field and possess 2-4 years of experience in regulatory affairs within the pharmaceutical industry. You must have a strong understanding of regulatory requirements and documentation, excellent written and verbal communication skills, attention to detail, and the ability to work independently while meeting deadlines. Proficiency in the Microsoft Office Suite is also required. This is a full-time, permanent position suitable for individuals with 2-4 years of experience in regulatory affairs or a similar role. The job offers benefits such as cell phone reimbursement, commuter assistance, flexible schedule, provided food, health insurance, internet reimbursement, leave encashment, life insurance, paid sick time, paid time off, and provident fund. You will be expected to work in person during day, evening, or fixed shifts from Monday to Friday. Additional benefits include a joining bonus, performance bonus, quarterly bonus, shift allowance, and yearly bonus. If you meet the qualifications and are interested in this position, please ensure to submit your application before the deadline on 13/03/2025. The expected start date for this role is 17/03/2025.,