Jobs · Legal · New York

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.

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