Project Manager - Regulatory Operations (Hybrid)

Position Overview The Project Manager, Reg Ops, role will partner closely with Director, Regulatory Affairs Operations & Intelligence, to support regulatory intelligence activities that ensure compliance of new and currently marketed products, taking into consideration current and proposed changes in regulatory requirements and standards globally. Providing support to administrative registration activities to facilitate timely regulatory submissions and market authorization/approvals. The Project Manager, Reg Ops role leads coordination efforts with cross-functional stakeholders for regulatory intelligence activities to evaluate regulatory impacts, support compliance strategies, and facilitate timely implementation. This role manages regulatory-related projects, tracking performance metrics, and ensuring alignment across teams and stakeholders. This includes leading document control processes to ensure quality and compliance of procedural documentation and supports regulatory operations project management. The position plays a critical role in maintaining regulatory readiness and supporting market authorization efforts for new and existing products. Responsibilities Responsible for proactively keep abreast of changes in global laws, regulations, standards/guidance and assess their impact and make recommendations to ensure compliance and provide regular reporting across the organization on key developments that impact product and/or processes and/or business directly. Responsible for the coordination of regulatory intelligence processes Responsible for assigning and organizing assessments of global laws, regulations, standards, and guidance with cross-functional stakeholders to ensure timely evaluation and alignment. Track implementation activities and follow up with stakeholders to ensure completion and accountability. Monitor and report on key performance indicators (KPIs) to measure effectiveness and identify areas for improvement. Maintain tracking and trending activities to support strategic decision-making and continuous improvement. Responsible for document control Responsible for updating and controlling procedure documents and forms to ensure accuracy, consistency, and compliance with internal and external standards. Ensure all documents meet established quality and regulatory requirements. Support the management of document lifecycle processes, including version control, review, and approval workflows. Responsible for Regulatory operation project management Responsible for organizing project objectives, managing detailed project plans, and establishing timelines and milestones to ensure successful execution. Allocate resources effectively and ensure project teams have the necessary tools and information to meet deliverables. Assemble and govern project teams, facilitate communication, and resolve conflicts to maintain momentum. Identify potential risks and develop mitigation strategies to minimize impact on outcomes. Monitor project progress, track KPIs, and provide regular updates to stakeholders to ensure transparency and alignment. Required Skills and Competencies Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently. Completes administrative tasks correctly and on time. Follows instructions and responds to management direction. Communicates changes and progress. Technical Skills - Assesses own strengths and development areas; Pursues training and opportunities for growth; Strives to continuously build knowledge and skills; Shares expertise with others. Demonstrated experience and proficiency with the Microsoft Office products (Word, Excel, PowerPoint, Access, Outlook) Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality. Analytical - Synthesizes complex or diverse information; Collects and researches data; Interprets internal and external business issues and recommends best practices Problem Solving – Solves complex problems; takes a broad perspective to identify innovative solutions. English read/write fluency a MUST. A second global language is a plus. Excellent ability to generate and maintain accurate records. Required Skills & Behaviors Independence – works independently, with guidance in only the most complex situations Leadership – may lead functional teams or projects Ethics - Treats people with respect; Ability to be honest and trustworthy; Works with integrity and ethically; Upholds organizational values. Teamwork – Balances team and individual responsibilities; Integrates continuous feedback loops; Contributes to building a positive team spirit; Puts success of team above own interests; Supports everyone's efforts to succeed. Contributes to building a positive team spirit. Shares expertise with others. Adaptability – Able to adapt to changes in the work environment. Manages competing demands. Changes approach or method to best fit the situation. Able to deal with frequent change, delays, or unexpected events. Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan. Communication - Listens and gets clarification; Responds well to questions; Speaks clearly and persuasively in positive or negative situations. Writes clearly and informatively. Able to read and interpret written information. Education and Experience B.S./B.A. (4-year Degree) and/or an equivalent combination of education and experience/background in life sciences, technical (engineering) or related field. Min 3 years of Medical Device Regulatory Affairs experience. Familiarity with International Regulations (e.g., US FDA 21 CFR 820, EU MDR 2017/745 and IMDRF/GHTF) required. Experience with regulatory data management systems preferred. Additional Information The position can be hybrid or in-person at any of our Insulet locations. Travel is estimated at 10% but will flex depending on business needs. Hybrid: NOTE: This position is eligible for hybrid working arrangements (requires on-site work from an Insulet office). #LI-Hybrid Additional Information: Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $89,400.00 - $134,100.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education. 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! At Insulet Corporation 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. (Know Your Rights) 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. (Know Your Rights) 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.

Salary : $89,400 - $134,100