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Regulatory Affairs Associate II

Spectraforce Technologies
United States, Illinois, North Chicago
Sep 29, 2026
Title: Regulatory Affairs Associate II Duration: 09 Months Location: North Chicago, IL Experience Level: 3-5 Years 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 Position Overview 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. Regulatory 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.