Sr Regulatory Affairs Specialist--Remote at AngioDynamics in Marlborough, Massachusetts

Job Description:

JOIN A TEAM COMMITTED TO IMPROVING PATIENT CARE


It takes a team of talented people to become one of the world's leading providers of innovative medical devices.


AngioDynamics is dedicated to improving patient outcomes by focusing on the development of disruptive and differentiated technologies that address unmet patient needs and supporting professional healthcare providers around the world in the delivery of high-quality patient care.


We accomplish this through:

• A Commitment to the Highest Standards of Quality


• Relentless Innovation


• Operational Excellence

Our employees receive the highest level of training and endeavor to be the best and the brightest in the medical device industry.


We are pleased to offer a comprehensive benefit plan that supports the overall health and wellness needs of our employees and their families.


JOB SUMMARY - To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

Responsible for determining the path to market for new and modifications to existing products in compliance with Regulations of intended market territory and for independently guiding teams on the required deliverables to support the Global Regulatory status of products distributed by AngioDynamics Inc.

Essential Duties and Responsibilities

• Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow up of submissions under review.
• Leads in the development and implementation of Regulatory strategies for new and modified medical devices.
• Researches and prepares recommendations on pathway for a new device, proposed device change or modification, independently (e.g. 510(k), PMA, Technical Documentation, Shonin, Canadian License).
• Apply scientific/technical knowledge to guide and strengthen development of regulatory submissions.
• Compile necessary information and prepare Regulatory license applications that meet specific country requirements to support international markets, as well as internal regulatory file documentation.
• Prepare and maintain Technical Documentation Files and IC Dossiers.
• Review and approve device labeling and advertising materials for compliance with Regulatory product approvals (submissions/licenses) as well as applicable country regulations; analyze, recommend, and assure implementation of appropriate changes.
• Maintain awareness of global regulatory requirements; review, create, develop, and implement global regulatory affairs procedures for marketed products to ensure company's regulatory compliance status.
• Review and recommend action on product and manufacturing changes in compliance with applicable regulations.
• Act as a core team member on development teams, providing Regulatory Affairs input and guidance throughout the product development cycle.
• Develop and maintain product listing/establishment details required to prepare documentation for product importation into US and International sites.
• Prepare Export Certificates (CFGs, CFS, etc.) - must have and apply knowledge of specific country requirements to lead in obtaining approvals from US regulatory agencies and International embassies.
• Prepare product and establishment registration/listing with Regulators (e.g., US/FDA, Customs, Europe, Australia, Health Canada, Brazil, LATAM and APAC countries).
• Collaborate with internal (Quality/Ops/R&D) and external (Partners/Distributors) groups to obtain documentation necessary to develop required Field Action reports to Regulators.
• Primary contact with global Regulatory partners.
• Lead regulatory projects as required. Effectively coordinate with cross-functional team members to achieve timely results.
• Contribute and lead as a team member on projects sustaining the Regulatory and Quality compliance of products and the continued enhancement of the organization.
• Support and maintain Quality initiatives in accordance with the Quality Policy.
• Continuously assess and support implementation of ways to improve Quality.
• This position has potential for travel to domestic and international facilities and meetings.
• May perform other duties as assigned.

Education and Experience

• Bachelor's Level of Degree in the scientific or technical discipline field of study.
• Eight years of demonstrated experience in Regulatory Affairs or equivalent knowledge.
• Master's degree, Medical industry experience, and/or RAC Certification preferred.

Skills/Knowledge

• Experience in the following computer software applications: Microsoft Office, Adobe Acrobat, Agile PLM System. Must have data analysis skills.
• In depth understanding of product development process and design control.
• Effective research, analytical and sound decision-making skills.
• Ability to work independently.
• Expert knowledge of FDA, MDR and other international regulations.
• Ability to manage contractors or other resources to complete and update compliant Post-market Clinical Follow-up studies and Clinical Evidence reports.
• Ability to effectively manage several projects simultaneously and independently to timely completion.
• Exceptional interpersonal skills.
• Strong organizational skills.
• Strong written and oral communication, technical writing and editing skills.
• Project management skills.
• Ability to effectively communicate both internally and externally.
• Ability to read and interpret documents such as safety rules, operating and maintenance, instructions, and procedure manuals. Ability to write routine reports and correspondence.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other legally protected status.


The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.

AngioDynamics does not accept resumes or candidate submissions from third-party recruiters and/or vendors who are not expressly under current written contract.


Your ultimate salary may vary depending on your job-related skills, knowledge, and experience. Apply Now