Navitas Life Sciences hiring Regulatory Affairs – Program Manager
- Regulatory Affairs – Program Manager at Navitas Life Sciences
- Key Responsibilities
- Qualifications and Skills
- Job Details
- How to Apply
Regulatory Affairs – Program Manager at Navitas Life Sciences
Navitas Life Sciences is looking for a talented and experienced Regulatory Affairs – Program Manager to join our team in Chennai. If you have a degree in pharma or life sciences and 10-12 years of experience in regulatory publishing and submissions, we want to hear from you!
Key Responsibilities
Regulatory Publishing and Submissions
As a Regulatory Affairs – Program Manager, your primary responsibilities will include:
- Regulatory Publishing: Overseeing the preparation and submission of regulatory documents.
- Regulatory Submissions: Managing the entire process of regulatory submissions to ensure compliance with global regulatory requirements.
Client and Team Management
- Client Management: Acting as the primary point of contact for clients, ensuring their needs and expectations are met.
- Team Management: Leading and managing a team of regulatory professionals to achieve project goals.
- Sales Support: Collaborating with the sales team to provide regulatory expertise during client pitches and proposals.
Presentation and Facilitation
- Presentation Skills: Developing and delivering presentations to clients and internal stakeholders.
- Facilitation Skills: Facilitating meetings and discussions to drive project progress and client satisfaction.
Qualifications and Skills
- Educational Background: Graduate or postgraduate degree in pharma, life sciences, or a related field.
- Experience: 10-12 years of experience in regulatory publishing and submissions.
- Communication Skills: Excellent verbal and written communication skills.
- Client and Team Management: Proven experience in managing clients and leading teams.
- Presentation and Facilitation: Strong presentation and facilitation skills.
Job Details
- Position: Regulatory Affairs – Program Manager
- Experience Required: 10-12 years in regulatory publishing and submissions
- Location: Chennai, India
- Company: Navitas Life Sciences
How to Apply
Interested candidates are encouraged to share their resumes with Roshini M at roshini.m@navitaslifesciences.com.