Regulatory Affairs Associate II

Mindlance
  • North Chicago, IL
  • Instant Apply
4 days ago

Job Description

Required Education: Bachelor s degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject
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. Job deliverables will include:
- 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.

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.

Experience Level = 3-5 Years

EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

Numbers & Facts

LocationNorth Chicago, IL

Skills

  • Analysis Skillsunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Change Controlunmatched
  • Chemistryunmatched
  • Communication Skillsunmatched
  • Content Managementunmatched
  • Corporate Policiesunmatched
  • Cross-Functionalunmatched
  • 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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