Director of Regulatory Affairs - RespirTech (Plymouth, MN)

Job Title Director of Regulatory Affairs - RespirTech (Plymouth, MN) Job Description Director of Regulatory Affairs – RespirTech (Plymouth, MN) The Director of Regulatory Affairs will lead the Philips RespirTech InCourage Vest Therapy Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/quality management system (QMS) responsibilities. Your role: Lead Regulatory Affairs strategy end-to-end execution (product inception through lifecycle management), driving innovation, actively providing value-added regulatory affairs input and deliverables for new 510k product introductions and product changes. Use metrics and key performance indicators to drive regulatory and quality decision making, meaningful actions, and continuous improvement. Lead the development and execution of regulatory strategies to maintain current products and bring new products to the market in an efficient manner. Develop and deploy regulatory resources in an efficient and effective manner. Represent regulatory affairs on the management team. Be able to articulate compliant regulatory strategy as well as manage operational matters such as Annual Operating Plan (AOP) development. Proactively build regulatory capabilities within the business. Provide practical interpretation/guidance of regulations, standards and input including risk assessment to support business decision making. Build proactive, robust, strategic relationships with external stakeholders (FDA, NBs, CAs, MedTech forums etc.) to influence and shape the external regulatory landscape across the domains relevant to the business unit innovation agenda. Ensure compliance with regulatory requirements and internal procedures. Empower and enable regulatory affairs and quality team members to foster a culture of collaboration and confident decision-making when working in cross-functional programs and projects. Manage/oversee execution of inspection readiness activities, including active inspection support. Participate in the coordination and execution of the internal audit program. Manage/oversee recall efforts, compliant handling, failure investigation, and adverse event reporting. Reporting to the Business Leader, you will lead and enable strong cross-functional partnerships with key stakeholders including R&D, Marketing, Quality, Clinical Affairs and other functions at all levels within the Business Unit. This role may require travel up to 10%. You're the right fit if: You’ve acquired 10+ years of experience working in Regulatory Affairs and/or Quality/Quality Operations within the FDA regulated Medical Device industry, including 3+ years of experience and a strong track record in successfully leading/managing Regulatory Affairs and/or Quality teams. Your skills include: Extensive experience/knowledge of global medical device regulations, requirements, and standards (ISO 13485, ISO 14971, 21 CFR 820, etc.) A proven track record leading cross-functional/diverse teams in a matrix organization, with challenging goals, with experience working in smaller companies desired. Experience in building/fostering strategic relationships with external stakeholders (e.g. Notified Bodies, FDA, Competent Authorities). You have a Bachelor’s Degree (required) in Engineering, Life Sciences, Quality, Regulatory or comparable disciplines. You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position. You’re an entrepreneur at heart who thrives when working with a small team to deliver big results. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an office role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose. Learn more about our culture. Philips Transparency Details The pay range for this position in Plymouth, MN is $171,000 to $273,000. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here. At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. Additional Information US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future. Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN.

#LI-PH1