Global Product Monitoring Vigilance Report Writer (hybrid) page is loaded

Global Product Monitoring Vigilance Report Writer (hybrid)

Please note that this is a hybrid role that requires attendance at the London Hammersmith office 3 days per week

The Global Product Monitoring Vigilance Report Writer: develops, establishes, and maintains quality assurance methodologies, systems, and medical device industry best practices which meet customer, regulatory, and client requirements; serves as a post-market vigilance (reportable event) and surveillance subject matter expert and representative to improve awareness, visibility, and communication on quality/compliance initiatives to support departmental, divisional, and corporate quality goals and priorities; works on problems of diverse scope where analysis of data requires evaluation of identifiable factors; demonstrates good judgment in selecting methods and techniques for obtaining solutions; and networks with senior internal and/or external personnel in own area of expertise.

Responsibilities:

• Responsible for the assessment, follow-up, coding, and vigilance activities for complaints globally.

• Author, peer review, and approve vigilance reports to ensure on time submissions to the appropriate regulatory authorities.

• Support management in day-to-day operations in a fast-paced work environment; Support proper coding of complaints and reportable events.

• Collaborate with engineering, complaint investigation laboratory, medical and other internal staff as applicable to review events, coding, and investigation results to support regulatory reporting compliance occurs per procedures, standards, and regulations.

• Contribute to departmental non-conformances escalated into CAPA System

• Serve as a subject matter expert for post-market and complaint handling regulatory questions and inquiries.

• Support internal and external audits and inspections.

• Assist with special projects, as assigned, with minimal supervision.

• Perform other duties as required.

Minimum Requirements:

• Bachelor’s degree or appropriate combination of relevant education and experience.

• Demonstrated experience in medical device complaint triage and vigilance reporting or clinical experience in diabetes disease management or diabetes device support.

Preferred Skills and Competencies:

• Strong proficiency in common computer applications such as Microsoft Office (Excel, Word, Outlook) and complaint database applications.

• Effective verbal and written communication skills.

• Ability to generate, verify, and maintain accurate records.

• Must have analytical skills, be detail oriented, and have good interpersonal skills.

• Demonstrated ability to influence without authority.

• Ability to organize, judge priorities, and escalate when applicable.

• Strong emphasis and understanding of a formalized medical device Quality Management System.

• Direct experience of writing and filing global vigilance reports within the medical device industry.

• Working knowledge/experience with global, multi-country vigilance reporting requirements for medical devices and demonstrated knowledge of country-specific differences and requirements.

• Experience in dealing directly with regulatory bodies is highly desired.

• BSN with diabetes experience, Registered or Licensed Dietician or Diabetic Educator, preferred.

Travel and Physical Requirements:

• General office environment – may sit for long periods of time.

• This position requires extensive computer use.

• May require up to 10% travel

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

Please read our Privacy Notice to learn how Insulet handles your personal information when you apply for a vacancy with us here .

About Insulet

Insulet Corporation is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Insulet employees are all focused on the same goal — to make a difference. Our relentless passion is to simplify life for people with diabetes. We excite and empower employees to bring their best selves to work through a culture that supports a healthy work and life balance. We set the bar high to meet customer needs, and our priority is to ensure our employees are equipped and supported to help us get there. We foster and celebrate curiosity, innovation, and learning. Our teams work collaboratively and are empowered to drive the best actions for our customers. Our innovation spirit and customer-centric focus position us as global pioneers — leading the way to improve health outcomes with revolutionary medical devices while breaking down barriers to access.