What do we offer you?
- Competitive salary and benefits package
- Remote work opportunities
- Professional development and growth opportunities
- Collaborative and supportive team environment
- Chance to make a significant impact on a global scale
- Work-life balance
Who are you?
We are looking for a dedicated and experienced Regulatory Affairs Specialist to join our team. You will be responsible for providing support throughout the entire submission lifecycle. Here are some key skills and qualifications we are seeking:
- Bachelor's degree in a related field.
- Experience in regulatory affairs within the pharmaceutical industry.
- Strong knowledge of regulatory requirements.
As a Regulatory Affairs Specialist, your day-to-day will involve managing and coordinating various aspects of regulatory submissions. This is a hands-on role where you will be directly contributing to the success of product approvals.
- Participate in initial submission planning and review required documentation.
- Compile and prepare regulatory documents, information, and technical files.
- Review submission packages and identify necessary documentation for local regulatory authorities.
- Support approval and post-approval activities, ensuring timely system updates.
- Manage submission archival and liaise with RA support functions.
You’ll be working remotely for a globally recognized pharmaceutical company committed to improving patient health. We offer a supportive and collaborative environment where you can utilize your skills and grow your career.
- Remote work opportunity.
- Supportive team environment.
- Opportunities for professional development.
Excited about this Regulatory Affairs Specialist opportunity? Apply now and become a key part of our team. This Regulatory Affairs Specialist role offers a fantastic chance to leverage your skills and make a real difference in the pharmaceutical industry. Don't miss out on this opportunity to become a Regulatory Affairs Specialist.