Regulatory Writer - Veeva RIM Configuration (Regulatory affairs)

Education:
o Bachelors or Masters degree in Life Sciences, Regulatory Affairs, or required fields
Experience:
o 5+ years of experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry.
o Exposure to Veeva RIM configuration and integrations
o Experience with full-stack development and a solid understanding of the software development lifecycle (SDLC).
o Familiarity with global regulatory processes, especially those of FDA, EMA, and Health Canada.
o Experience with other regulatory software platforms and tools.
o Proven track record of leading cross-functional projects and teams in a global
environment.

Skills:
o Strong technical aptitude and the ability to manage complex system
integrations.
o Excellent problem-solving skills and the ability to work under pressure in a
dynamic environment.
o Outstanding communication and interpersonal skills, with the ability to influence
and manage stakeholders effectively.
o Strong project management skills with a focus on regulatory projects.