Platform Principal Regulatory Affairs Specialist

Job not on LinkedIn

🔥 12 hours ago

⛷️ Utah – Remote

⛷️ Utah – Remote

⏰ Full Time

🔴 Lead

🚔 Compliance

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Merit Medical Oncology

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1987

🤝 B2B

💰 $4.2M Venture Round - Cianna Medical on 2016-10

B2B

Merit Medical Oncology is a division/specialty of Merit Medical Systems focused on devices and procedural solutions for oncologic interventions. It is part of Merit Medical Systems, a global manufacturer founded in 1987 that designs and markets proprietary disposable medical devices used in interventional, diagnostic and therapeutic procedures across cardiology, radiology, oncology, critical care and endoscopy. Merit Medical Oncology supports hospitals and physicians worldwide with products (e. g. , biopsy, embolotherapy, drainage, and other oncology-related interventional tools), clinician education and training, regulatory and product documentation, and global distribution and customer support.

📋 Description

• Collaborates with key stakeholders to ensure alignment of regulatory goals and objectives with the strategic priorities of the business. • Develops and maintains strong strategic partnerships with project team members, including Marketing, R&D, Operations, Clinical Affairs and Quality Assurance. • Ensures all regulatory activities for assigned platform and operations projects comply with evolving global regulatory requirements. • Maintains product knowledge within the team and ensures essential data is gathered and organized in support of global submissions. • Partners with the Regional RA team in the development, alignment and execution of Regulatory strategies for platform and operations projects and changes, upholding rigorous standards of accuracy, timeliness, compliance and excellence in regulatory strategy. • In collaboration with Regional RA, represents Merit effectively in interactions with Regulatory authorities, strengthening Merit's reputation and credibility. • Supports and suggests continuous improvement of regulatory processes, procedures and policies. • Ensures compliance with relevant regulatory requirements. • Ensures project teams are informed of new and pending changes in regulation and evolving interpretation of regulation and how they will be impacted. • Ensures the timely maintenance of regulatory data with a high degree of accuracy and compliance. • Supports Regulatory Affairs in due diligence activities to ensure regulatory risks and integration needs are clearly articulated and understood. Coordinates with Regional RA on the integration of new acquisitions. • Supports and when needed represents Regulatory Affairs in audits/inspections leading to successful outcomes. • Performs other duties and tasks as required.

🎯 Requirements

• Education and/or experience equivalent to Bachelor’s degree in a technical field such as in the biological, physical, engineering, material science, regulatory, legal or related disciplines. • 15+ years of Regulatory Submissions experience in the medical device industry. • Considered an expert with demonstrated knowledge, use, and/or application of applicable medical device regulations (Quality System Standards/Regulations/Laws, including but not limited to ISO 13485, etc., Design Controls). • Identify and frame concepts with a basic understanding of business impact.

🏖️ Benefits

• Medical/Dental & Other Insurances (eligible the first of month after 30 days) • Low Cost Onsite Medical Clinic • Two (2) Onsite Cafeterias • Employee Garden | Gardening Classes • 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays • 401K | Health Savings Account