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
Location
North 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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