Regulatory Affairs Associate

Katalyst Healthcares & Life Sciences
  • North Chicago, IL
  • Instant Apply
20 days ago

Job Description

Responsibilities:
  • Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.
  • Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports).
  • Review/approval of engineering study protocols/reports and validation study protocols/reports.
  • Review and approval of manufacturing changes for Class III implantable medical devices.
  • May require an advanced degree and 3 to 5 years of direct experience in the field.
  • Recent experience with Class III implantable medical devices; Proven successful track record of authoring/submission/approval of Class III implantable PMA supplements; knowledge of FDA PMA guidance documents and CFR regulations.
  • Relies on extensive experience and judgment to plan and accomplish goals. Performs a variety of tasks.
  • May lead and direct the work of others. A wide degree of creativity and latitude is expected

Required Experience:

  • 6 years pharmaceutical or industry related experience.
  • 3-5 years in quality systems or cross-functional project management

Preferred Experience:

  • 6 years pharmaceutical experience including 5 years in regulatory affairs or 5 years in Discovery, R&D, or Manufacturing
  • Experience working in a complex and matrix environment
  • Strong oral and written communication skills
  • This contractor will work with internal and external partners in order to deliver products to patients.
  • Prepare regulatory submissions, including new applications and amendments, renewals, annual reports, supplements and variations under limited supervision and responds to regulatory information.
  • Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions
  • Manages preparation for agency meetings and manages content of pre-meeting submissions.
  • Manages products and change control with an understanding of regulations and company policies and procedures.

Required Education:

  • Bachelor's degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject.

Numbers & Facts

LocationNorth Chicago, IL

Skills

  • Analysis Skillsunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Change Controlunmatched
  • Chemistryunmatched
  • Code of Federal Regulationsunmatched
  • Communication Skillsunmatched
  • Content Managementunmatched
  • Corporate Policiesunmatched
  • Cross-Functionalunmatched
  • FDA (Food and Drug Administration)unmatched
  • Governmentunmatched
  • Implantsunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Pharmacologyunmatched
  • Pharmacyunmatched
  • Presentation/Verbal Skillsunmatched
  • Product Managementunmatched
  • Project/Program Managementunmatched
  • Regulationsunmatched
  • Regulatory Submissionsunmatched
  • Research & Development (R&D)unmatched
  • Research Protocolsunmatched
  • Technical Supportunmatched
  • Validation Planunmatched
  • Writing Skillsunmatched

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