The Junior Regulatory Consultant provides hands-on support for regulatory documentation, standards management, and submission preparation. They are responsible for maintaining compliance records, updating technical documents, and assisting with Quality Management System documentation.
The Senior Director will lead the Pharmaceutical Writing Services group, providing scientific and operational leadership for complex clinical submission programs and medical device clinical evaluations. They are responsible for authoring high-level regulatory documents, mentoring staff, and serving as a primary technical authority for clients and project teams.
