Regulatory Affairs Associate I
Planet Pharma · Skaneateles, NY · 1 mo ago
LegalContract
About the role
Responsible for the global coordination and the preparation of documents/packages for regulatory submissions. In this position you will also review and evaluate technical and scientific data and reports required for submission in support of global products.
Pay
35-45/hr depending on experience
Skills
- Familiar with USA and OUS device regulations (specifically EU device regulations)
- Experience with RA strategy development
- Experience with working with cross‑functional team members
- Experience with interaction with external regulators (FDA, TUV)
- Experience with working with medical devices
Responsibilities
- Supports regulatory project plan execution
- Maintain awareness of regulatory requirements and ensure continued learning
- Maintain regulatory files in a format consistent with requirements
- Participate as an active team member of project teams as required
- Compile and prepare responses to questions from regulatory authorities according to plan
- Edit and proofread regulatory documentation
- Assist in preparation and review of labeling, SOPs, and other departmental documents
- Compile under supervision regulatory documents for submission
- Track status and progress of regulatory documentation
- Understand Regulatory Affairs' position in small project teams
Qualifications
- Knowledge of regulations
- Scientific knowledge
- Administrative and project management skills
- Ability to contribute to multiple projects from a regulatory affairs perspective
- Ability to multitask and prioritize
- Interpersonal and communication skills
- Technical system skills (e.g. word processing, spreadsheets, databases, online research)
- Proofreading and editing skills
Education and/or Experience: Bachelors degree or country equivalent in a relevant scientific discipline. Suitable candidates with a non‑scientific degree may be accepted and undertake further training e.g. under an apprenticeship or similar post‑graduate qualification. Regulatory experience preferably within a healthcare environment.