Senior Manager, Regulatory Affairs

🕒 vor 1 Monat

🐊 Florida, New Jersey, +1 weitere Bundesländer – Remote

🐊 Florida – Remote 🏖️ New Jersey – Remote 🗽 New York – Remote

💵 $155.677 - $202.380 / Jahr

⏰ Vollzeit

🟠 Senior

🚔 Compliance

Jetzt Bewerben

Ähnliche Remote-Jobs finden

E-Mails für Remote-Jobs erhalten

📊 Überprüfen Sie Ihre Lebenslauf-Bewertung für diese Stelle

Verbessern Sie Ihre Chancen auf ein Vorstellungsgespräch, indem Sie Ihre Lebenslauf-Bewertung vor der Bewerbung überprüfen.

Lebenslauf hochladen

QuidelOrtho

WebsiteLinkedInAlle Stellen

5001 - 10000 Mitarbeiter

⚕️ Krankenversicherung

💊 Pharmazie

🔬 Wissenschaft

Healthcare Insurance • Pharmaceuticals • Science

QuidelOrtho ist ein globales Unternehmen, das sich darauf konzentriert, Diagnosedaten in umsetzbare Erkenntnisse für bessere Gesundheitsergebnisse zu verwandeln. Sie bieten eine breite Palette von Diagnoselösungen an, einschließlich COVID-19-Testkits für zu Hause, klinische Chemie, Immunoassay-Produkte, Molekulardiagnostik und automatisierte Lösungen für Gesundheitsdienstleister. Ihre Produkte sind für den Einsatz in verschiedenen Settings ausgelegt, von zu Hause bis zum Krankenhaus und vom Labor bis zur Klinik, um zuverlässige und schnelle Diagnoseergebnisse zu gewährleisten. QuidelOrtho strebt danach, eine gesündere Zukunft zu schaffen, indem sie Echtzeitinformationen und branchenführende Expertise bietet.

Beschreibung

• Manage and support a team of managers and employees of different levels. • Responsible for developing and implementing local strategy and leading the day-to-day regulatory affairs on base business operations and new product development projects within the Transfusion Medicine Business Unit. • Reviewing and interpreting regulations/guidance documents to develop a regulatory strategy to support Transfusion Medicine project teams in terms of regulatory submission pathway, clinical efficacy requirements, predicate device selection, submission requirements, timing, and risks. • Interact with US FDA and/or EU Notified Body regulatory personnel (including Corporate International RA and/or country RA) to define submission content, expedite pending applications, and resolve regulatory matters. • Responsible for the final review of critical regulatory documents planned for regulatory submissions and responses to regulatory agencies as needed. • Make judgments about the operational impact of proposed actions, and identify and interact with appropriate resources to successfully achieve company and regulatory strategy objectives. • Reviews/ interprets product-specific regulatory issues that may have a material impact on the business, the corporation, or the customer; develop strategic and tactical responses to influence a reasonable and compliant regulatory environment. • Represent QuidelOrtho to US and EU regulatory agencies and interact with Health ministry personnel to expedite pending applications, resolve regulatory matters, and manage development meetings for regulatory submissions. • Identify and/or lead process improvement projects to streamline current activities and increase department efficiencies. • Development goals, such as webinars, reviewing FDA website and articles, reading journals, and attendance at industry meetings, to expand knowledge and skill set in Regulatory affairs. • Coach, mentor junior staff. Provide guidance to business partners and junior regulatory staff regarding regulatory requirements including indications of risks and appropriate timing for approvals for planning purposes. • Perform other work-related duties as assigned.

🎯 Anforderungen

• Bachelor’s degree in a scientific or related discipline; or equivalent combination of education and experience. • 10 years+ of experience in a regulated In Vitro Diagnostics and/ or Biologics Industry. • 7+ years of experience developing and executing regulatory strategies for complex projects under product development or post-market changes requiring a US FDA submission (510(k), PMA and BLA or associated supplements and Annual Reports). • Review and approval of product labeling and promotional and advertisement brochures and multimedia content. • Coordinate and submit Pre-Sub meeting requests and associated regulatory strategic information and direct interaction with FDA product review branch(s). • Previous people management experience. • Excellent interpersonal, teamwork, and verbal/written communication skills. • Good organizational skills and an ability to manage multiple tasks/projects/priorities. • The ability to demonstrate model behavior and understand priorities and encourage others to drive for results will be needed. • Ability to mentor and coach junior level staff as well as cross-train with peers.

🏖️ Vorteile

• medical, dental, vision, life, and disability insurance • 401(k) plan • employee assistance program • Employee Stock Purchase Plan • paid time off (including sick time) • paid Holidays