Philips Regulatory Affairs Manager in Cambridge, Massachusetts
If you are a Colorado resident and this role is a field-based or remote role, you may be eligible to receive additional information about the compensation and benefits for this role, which we will provide upon request. You may contact 888-367-7223, option 5, for assistance.
In this role, you have the opportunity to
Lead individual contributors, generally operating at a more senior level formulating the medium term regulatory policy into a regulatory strategic plan, while also being involved in developing, modifying and executing
company regulatory strategies and policies that affect immediate operations.
You are responsible for
Leads business unit regulatory resources and shares the workload (hands on) to ensure timely product registrations, regulatory planning for new product introductions (ventilators and related devices/accessories) and product changes, guidance on risk assessment, and required corrective actions to meet regulatory requirements, as well as leadership and guidance on global regulatory strategy, such as CE Marking, product registrations, and clinical evaluations.
Exercises supervision in terms of budgets, schedules, methods, staffing and performance. Establishes operational objectives and work plans, and delegates assignments to subordinates.
Works on issues where analysis of situations or data requires an in-depth knowledge of organizational objectives.
Involved in developing, modifying and executing company regulatory policies that affect immediate operations.
Regularly interacts with senior management or executive levels on matters concerning several functional areas and/or customers.
Responsible for product registrations/approvals.
Responsible for working with PCA Q&R Business Leader to prepare for compliance with new EU MDR (Medical Device Regulation).
Keep abreast of current regulatory procedures and changes. Participates in direct interaction with regulatory agencies on defined matters.
Recommend and develop strategies and create detailed written regulatory plans
Responsible for the coordination and preparation of document packages 510(k) pre-market notification, technical file and design dossiers for CE marking, China CFDA domestic registrations and support worldwide product registrations per in-country regulations
Identify potential regulatory approvals risks based on changes in regulations, standards country specific issues or other unique characteristics of the project.
Drives improvement in regulatory aspects of the Quality System, developing processes and documenting procedures to ensure an effective Quality System. Review and recommend changes for design process and manufacturing procedures to maintain quality and regulatory compliance
Responsible for ensuring compliance with regulatory procedures and updating the procedures when new regulatory requirements become effective.
Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objectives.
May represent Philips in an international committee chartered to develop an applicable standard.
Review and approve advertising, promotional items and labeling for regulatory compliance.
Coordinate testing required to support regulatory submissions.
Strengthen and build clinical & regulatory capabilities.
Develop talent and build up Regulatory as a value–added business partner.
Manage, mentor and coach BU regulatory team in their development.
Maintain regulatory files and tracking databases as required.
Must ensure that training assignments remain current.
To succeed in this role, you should have the following skills and experience
Bachelor’s degree (Master’s or PhD preferred) preferably in Regulatory Affairs and/or a science related field or equivalent experience in the medical device industry.
Minimum of 8 years of experience in the medical device industry (EU MDD, US FDA class II, class III) or 12 years of regulatory experience if the candidate’s background does not include class III devices.
Must have personal “hands on” experience with successful preparation, submission and clearance of 510(k)s. Regulatory & technical competency is also expected with CE marking / technical files experience is strongly preferred.
Experience in supporting international registrations, clinical investigations and clinical evaluation reports.
RAPs RAC preferred.
Strong background in Design Controls.
Proficient knowledge of medical device regulations (21CFR), FDA law, MDD/EU MDR, MDSAP and other global laws and regulations and standards.
Understand LEAN concepts, methodologies and deployment.
May require limited travel annually.
Why should you join Philips?
Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways.
To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips pageon our career website, where you can read stories from our employee blog. Once there, you can also learn about our recruitment process, or find answers to some of the frequently asked questions.
It is the policy of Philips to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to race, color, ethnicity, religion, gender, pregnancy/childbirth, age, national origin, sexual orientation, gender identity or expression, disability or perceived disability, genetic information, citizenship, veteran or military status or a person’s relationship or association with a protected veteran, including spouses and other family members, marital or domestic partner status, or any other category protected by federal, state and/or local laws.
As an equal opportunity employer, Philips is committed to a diverse workforce. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.
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