Philips
Sr. Manager Regulatory Affairs
Philips, Gainesville, Florida, us, 32635
Job Title Sr. Manager Regulatory Affairs Job Description
The Senior Manager Regulatory Affairs will play a critical role within Philips’ Clinical Informatics organization by
leading regulatory projects for Philips’ Disease Management Solution
products ,
ensuring
and maintaining global accurate regulatory strategy and market access ,
directly impacting the lives of patients around the world.Your role:Leading project teams for end-to-end regulatory affairs input
and deliverables for new product introductions and product changes across the globe.Through end-to-end regulatory processes, ensuring safe and effective products / solutions are brought to market, on time, and sustained throughout life cycle via compliant, innovative regulatory strategies.Provide critical input on regulatory risk assessments
to support portfolio selection.Collaborate and extend in proactive, strategic relationships with external stakeholders (Notified Bodies, FDA, Competent Authorities, and other Regulatory bodies) to ensure that requirements are known early during strategy development, enabling rapid market access with the current portfolio in connection with future innovations.Building FDA regulatory submissions strategy
for the products portfolio, providing related guidance to cross functional dedicated team and authoring 510K submissions.Leading and enabling strong cross-functional partnership between Regulatory Affairs and all key stakeholders including R&D, Marketing, Quality, Clinical Affairs, and other functions at all levels within the business, and the local Regulatory Affairs teams in the Philips international markets organization.This
Hybrid
role may require travel up to 10%.You're the right fit if:You have a minimum of 10 years’ experience in FDA Regulated Medical Device/HealthTech environments, with
extensive knowledge and experience authoring 510K’s, PMA’s, Pre-submissions, IDE, Technical Files/Design Dossiers, and other regulatory submissions.You have 5 years’ experience leading product development teams in satisfying registration requirements to bring products to market on time.You have detailed knowledge of MDD/MDR, MedDev’s, FDA QSR’s, FDA SaMD related and cybersecurity guidance’s, ISO 13485, ISO 14971, IEC 62304, and applicable medical device regulations/standards for the EMEA market, including SaMD.You have practical knowledge and experience with Advanced Visualization SaMD for diagnosis support (highly desired).You have proven experience building strategic relationships with external stakeholders (e.g., Notified Bodies, FDA, Competent Authorities).You have experienced formulating and implementing global regulatory strategies to ensure compliance with worldwide regulations to improve product market access.You’re an excellent communicator and collaborator who can build and maintain cross-functional partnerships in support of business successes.You’re self-directed with a strong work ethic and with an ability to work in a goal-oriented environment.You have a minimum of a
Master’s degree (REQUIRED), preferably in Regulatory Affairs or a Life Sciences field.You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this
position
.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.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.Read more about
our employee benefits
.If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion
here
.Philips Transparency Details:The pay range for this position is $104,000 to $178,000, annually. The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity.#LI-PH1This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.Philips is an
Equal Employment and Opportunity
Employer/Disabled/Veteran
and maintains a drug-free workplace.
#J-18808-Ljbffr
The Senior Manager Regulatory Affairs will play a critical role within Philips’ Clinical Informatics organization by
leading regulatory projects for Philips’ Disease Management Solution
products ,
ensuring
and maintaining global accurate regulatory strategy and market access ,
directly impacting the lives of patients around the world.Your role:Leading project teams for end-to-end regulatory affairs input
and deliverables for new product introductions and product changes across the globe.Through end-to-end regulatory processes, ensuring safe and effective products / solutions are brought to market, on time, and sustained throughout life cycle via compliant, innovative regulatory strategies.Provide critical input on regulatory risk assessments
to support portfolio selection.Collaborate and extend in proactive, strategic relationships with external stakeholders (Notified Bodies, FDA, Competent Authorities, and other Regulatory bodies) to ensure that requirements are known early during strategy development, enabling rapid market access with the current portfolio in connection with future innovations.Building FDA regulatory submissions strategy
for the products portfolio, providing related guidance to cross functional dedicated team and authoring 510K submissions.Leading and enabling strong cross-functional partnership between Regulatory Affairs and all key stakeholders including R&D, Marketing, Quality, Clinical Affairs, and other functions at all levels within the business, and the local Regulatory Affairs teams in the Philips international markets organization.This
Hybrid
role may require travel up to 10%.You're the right fit if:You have a minimum of 10 years’ experience in FDA Regulated Medical Device/HealthTech environments, with
extensive knowledge and experience authoring 510K’s, PMA’s, Pre-submissions, IDE, Technical Files/Design Dossiers, and other regulatory submissions.You have 5 years’ experience leading product development teams in satisfying registration requirements to bring products to market on time.You have detailed knowledge of MDD/MDR, MedDev’s, FDA QSR’s, FDA SaMD related and cybersecurity guidance’s, ISO 13485, ISO 14971, IEC 62304, and applicable medical device regulations/standards for the EMEA market, including SaMD.You have practical knowledge and experience with Advanced Visualization SaMD for diagnosis support (highly desired).You have proven experience building strategic relationships with external stakeholders (e.g., Notified Bodies, FDA, Competent Authorities).You have experienced formulating and implementing global regulatory strategies to ensure compliance with worldwide regulations to improve product market access.You’re an excellent communicator and collaborator who can build and maintain cross-functional partnerships in support of business successes.You’re self-directed with a strong work ethic and with an ability to work in a goal-oriented environment.You have a minimum of a
Master’s degree (REQUIRED), preferably in Regulatory Affairs or a Life Sciences field.You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this
position
.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.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.Read more about
our employee benefits
.If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion
here
.Philips Transparency Details:The pay range for this position is $104,000 to $178,000, annually. The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity.#LI-PH1This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.Philips is an
Equal Employment and Opportunity
Employer/Disabled/Veteran
and maintains a drug-free workplace.
#J-18808-Ljbffr