Regulatory Affairs Specialist
Department: Regulatory Affairs
Position: Specialist, Regulatory Affairs (RA)
Location: Ahmedabad
Qualifications: M. Pharm. / B. Pharm
Experience: 3-6 years
Job Description:
Join Baxter Pharmaceutical Solutions, a team of motivated employees dedicated to our mission. Regardless of role, each team member is deeply committed to our goals.
Key Responsibilities:
- Execute regulatory project plans
- Stay updated on regulatory requirements and ensure continuous learning
- Maintain regulatory files per requirements
- Actively participate in project teams
- Compile and prepare responses to regulatory authorities
- Edit and proofread regulatory documentation
- Assist in preparing and reviewing labeling, SOPs, and other documents
- Compile regulatory documents under supervision
- Track the status and progress of regulatory documentation
- Understand Regulatory Affairs’ role in small project teams
Important Details:
Selection Process: Interview
Mode of Interview: Face to face
Interview Rounds: HR
Walk-in Interview Details:
Virtual Walk-in Drive – Injectable Regulatory Affairs
Date: 5th June
Time: 9:30 AM – 5:30 PM
Location: Virtual walk-in drive
Contact: Arshav Thakkar
Register to attend the walk-in drive: Register Here
Equal Employment Opportunity (EEO):
Baxter is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
