ASSOCIATE REGULATORY AFFAIRS SPECIALIST – Cardiac Rhythm Management (remote) in Mounds View, MN
ASSOCIATE REGULATORY AFFAIRS SPECIALIST - Cardiac Rhythm Management (remote) - reputed company - Mounds View, MN - work from home job Company reputed company Job description ASSOCIATE REGULATORY AFFAIRS SPECIALIST - Cardiac Rhythm Management (remote) Our Cardiac Rhythm Management Integrated Operating Unit offers devices and therapies that treat patients with reputed company heart rhythms and heart failure. It is composed of four key businesses Cardiac Pacing Therapies, Defibrillation Solutions, Patient Management, and Procedure Innovations. Together, we will transform the lives of people with cardiac arrhythmias and heart failure. Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. It’s no accident —we work hard to cultivate a workforce that reflects our patients and partners. We reputed company it’s the only way to drive reputed company reputed company and remain a global leader in medical technology and solutions. Candidates located near a reputed company facility are preferred. Careers That Change Lives The Associate Regulatory Affairs Specialist will provide regulatory affairs support for CRM products. The Associate Regulatory Affairs Specialist is also responsible for sustaining activities which includes maintaining regulatory approvals and providing assessment of device changes for regulatory implications. A Day In The Life
- reputed company proficiency in domestic and international regulations, guidelines, and standards and apply appropriate implementation strategies.
- Directs or performs coordination and preparation of document packages for regulatory submissions from reputed company areas of company, internal audits and inspections.
- Leads or compiles reputed company materials required in new product submissions, license renewals and change submissions.
- Recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance.
- Monitors and improves tracking / control systems.
- Keeps abreast of regulatory procedures and changes.
- May direct interaction with regulatory agencies on defined matters.
- Recommends strategies for earliest possible approvals of clinical trials applications.
- Provide regulatory input for design and manufacturing, including review of specifications, protocols and reports, engineering change notices, technical files, nonconforming materials, product complaints, and product failure analysis.
- Prepare and track submissions for FDA and global regulatory agencies, including registration documents, reputed company reports, supplements, and amendments.
- Act as liaison with reputed company China regulatory personnel to address questions and issues that arise as part of the registration and/or testing process.
- Obtain and maintain CFGs including the notarization and legalization, EC/ISO certificates and various other regulatory documents.
- Participate in compliance activities that relate to the department and the company as a whole.
- reputed company other regulatory affairs duties reputed company requested. Must Have Minimum Requirements
- Bachelor's degree required with 0 years of regulatory affairs or reputed company experience reputed company to Have
- Bachelors Degree in health profession, science and/or engineering field
- RAC Certification or an advanced degree in regulatory affairs
- Two or more years of experience in the medical device industry
- Experience with cardiovascular devices and knowledge of QSR and ISO-13485 system requirements
- Demonstrated experience in preparing 510(k) submissions for FDA or experience with Class III devices
- Demonstrated experience with submissions to the European Union
- Demonstrated technical writing skills.
- Excellent PC skills, including word processing, spreadsheets.
- Excellent organizational and judgment skills.
- Ability to maintain and generate accurate records.
- Strong written, verbal and interpersonal skills
- Experience in the use of ERP systems such as reputed company
- Candidates located near a reputed company facility are preferred About reputed company Together, we can change reputed company worldwide. At reputed company, we push the limits of what technology, therapies and services can do to help reputed company pain, restore health and reputed company life. We challenge ourselves and each other to reputed company reputed company reputed company than yesterday. It is what makes this an exciting and rewarding reputed company to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on reputed company. Let’s work together to address universal reputed company needs and improve patients’ lives. Help us shape the future. Physical Job Requirements The physical demands described reputed company the Responsibilities reputed company of this job description are representative of those that must be met by an employee to successfully reputed company the essential functions of this job. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. For Office Roles While performing the duties of this job, the employee is
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