Director Infusion Systems
Becton Dickinson
Director Infusion Systems
Job Description
Job Description Summary
Job Description
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
We believe that the human element, across our global teams is what allows us to continually evolve. Join us and discover an environment in which you will be supported to learn, grow, and become your best self. Become a maker of possiblewith us.
The Director of Regulatory Affairs reports directly to the Senior Director of Regulatory Affairs. This position is responsible for supporting MMS Infusion products consisting of Medical Devices a along with associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. Support will consist of new product development, sustaining, and end of life activities. The Director will oversee the hiring, training, and career development of their reports.
Responsibilities:
- Lead and develop direct report associates to ensure regulatory compliance
- Problem solve and escalate regulatory and compliance issues to senior management as vital
- Provide effective leadership and team development, effective communication, and quick responses to customers
- Drive continuous improvement in internal processes and customer satisfaction
- Identify, develop, and mentor impactful regulatory talent
- Author and organize regulatory submission content (510(k), Technical Files, etc.)
- Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non-Medical device products and software
- Lead regulatory effort to comply with new and existing regulations (e.g., FDA Medical Device Regulations, EU-MDR)
- Support the monitoring, interpreting, and implementing of current and new regulatory requirements and international standards for U.S., EU., and RoW
- Assure that QMS requirements are followed and executed consistently from RA perspective
- Oversee efforts for Technical File creation and remediation, collaborating with cross-functional teams for required content
- Support regulatory impact assessments for change controls and other RA/QA items from a review and approve level
- Assists in preparing, auditing, editing, and publishing registration documentation, as needed
- Support business export control (BEC) listing of product for release globally per RA requirements
- Support the review and approval of product labeling, promotional, and advertising materials as needed
- Performs other duties and assignments as required
Qualifications:
- Bachelor’s degree in RA, QA, engineering, or other science related discipline
- Advanced degree (e.g. MS, PhD) preferred
- RAPS RAC certification preferred
- Minimum of 10 years of directly related Regulatory Affairs experience in medical devices and/or in vitro diagnostic field
- Minimum of 7 years of personnel management (direct report) experience including performance evaluations/improvement, and career development
- Software experience including SaMD/SiMD is a plus
- Regulatory and Quality Information Management systems such as SAP, RIM, or related systems
- Digital literacy MS Word, Excel, PowerPoint, Teams
- Project Management experience
- Knowledge of global Regulatory Affairs requirements, regulations and standards
- Experience authoring regulatory submissions (US and Global)
- Strong prioritizing, interpersonal, communication, and analytical skills and the ability to multi-task disparate projects
- Ability to represent Regulatory Affairs in multiple environments (e.g. Marketing, R&D, and compliance) and work with all levels of personnel, including VP/GM
- Ability to partner with cross-functional colleagues to identify opportunities for regulatory innovation
- Read, analyze, and interpret regulatory literature and documents and effectively communicate information to peers and management
- Ability to work within a team environment and independently with minimum supervision
- Identify and communicate risks and mitigations associated with global regulatory strategies to cross-functional collaborators and act upon these items appropriately as an RA member
- Demonstrated leadership courage through openness to diverse views, candor in assessing and articulating difficult positions, and willingness to make changes when needed
- Ability to travel globally up to 10% of the time
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit https://bd.com/careers
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
Required Skills
Optional Skills
.
Primary Work Location
USA CA - San Diego TC Bldg C&DAdditional Locations
Work Shift
At BD, we are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.
Salary Range Information
$179,200.00 - $322,500.00 USD AnnualLocations
- San Diego, California, United States of America
Salary
180,000 - 280,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- proficiency in MS Word, Excel, PowerPoint, Teamsintermediate
- experience with Regulatory Affairs in medical devices and/or in vitro diagnostic fieldintermediate
- experience with personnel managementintermediate
- experience with Software including SaMD/SiMDintermediate
- experience with Regulatory and Quality Information Management systems such as SAP, RIM, or related systemsintermediate
- experience with Project Managementintermediate
- knowledge of global Regulatory Affairs requirements, regulations and standardsintermediate
- experience authoring regulatory submissions (US and Global)intermediate
- strong prioritizing, interpersonal, communication, and analytical skillsintermediate
- ability to multi-task disparate projectsintermediate
- ability to represent Regulatory Affairs in multiple environmentsintermediate
- ability to partner with cross-functional colleaguesintermediate
- read, analyze, and interpret regulatory literature and documentsintermediate
- effectively communicate information to peers and managementintermediate
- ability to work within a team environment and independently with minimum supervisionintermediate
- identify and communicate risks and mitigationsintermediate
- demonstrated leadership courageintermediate
Required Qualifications
- Bachelor’s degree in RA, QA, engineering, or other science related discipline (degree in ra)
- Advanced degree (e.g. MS, PhD) preferred (degree)
- RAPS RAC certification preferred (certification)
- Minimum of 10 years of directly related Regulatory Affairs experience in medical devices and/or in vitro diagnostic field (experience, 10 years)
- Minimum of 7 years of personnel management (direct report) experience including performance evaluations/improvement, and career development (experience, 7 years)
- Software experience including SaMD/SiMD is a plus (experience)
- Regulatory and Quality Information Management systems such as SAP, RIM, or related systems (experience)
- Digital literacy MS Word, Excel, PowerPoint, Teams (experience)
- Project Management experience (experience)
- Knowledge of global Regulatory Affairs requirements, regulations and standards (experience)
- Experience authoring regulatory submissions (US and Global) (experience)
- Strong prioritizing, interpersonal, communication, and analytical skills and the ability to multi-task disparate projects (experience)
- Ability to represent Regulatory Affairs in multiple environments (e.g. Marketing, R&D, and compliance) and work with all levels of personnel, including VP/GM (experience)
- Ability to partner with cross-functional colleagues to identify opportunities for regulatory innovation (experience)
- Read, analyze, and interpret regulatory literature and documents and effectively communicate information to peers and management (experience)
- Ability to work within a team environment and independently with minimum supervision (experience)
- Identify and communicate risks and mitigations associated with global regulatory strategies to cross-functional collaborators and act upon these items appropriately as an RA member (experience)
- Demonstrated leadership courage through openness to diverse views, candor in assessing and articulating difficult positions, and willingness to make changes when needed (experience)
- Ability to travel globally up to 10% of the time (experience)
Preferred Qualifications
- Advanced degree (e.g. MS, PhD) preferred (degree)
- RAPS RAC certification preferred (certification)
- Software experience including SaMD/SiMD is a plus (experience)
Responsibilities
- Lead and develop direct report associates to ensure regulatory compliance
- Problem solve and escalate regulatory and compliance issues to senior management as vital
- Provide effective leadership and team development, effective communication, and quick responses to customers
- Drive continuous improvement in internal processes and customer satisfaction
- Identify, develop, and mentor impactful regulatory talent
- Author and organize regulatory submission content (510(k), Technical Files, etc.)
- Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non-Medical device products and software
- Lead regulatory effort to comply with new and existing regulations (e.g., FDA Medical Device Regulations, EU-MDR)
- Support the monitoring, interpreting, and implementing of current and new regulatory requirements and international standards for U.S., EU., and RoW
- Assure that QMS requirements are followed and executed consistently from RA perspective
- Oversee efforts for Technical File creation and remediation, collaborating with cross-functional teams for required content
- Support regulatory impact assessments for change controls and other RA/QA items from a review and approve level
- Assists in preparing, auditing, editing, and publishing registration documentation, as needed
- Support business export control (BEC) listing of product for release globally per RA requirements
- Support the review and approval of product labeling, promotional, and advertising materials as needed
- Performs other duties and assignments as required
Benefits
- general: A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work.
- general: It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
- general: To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
- general: We welcome people with the imagination and drive to help us reinvent the future of health.
- general: At BD, you’ll discover a culture in which you can learn, grow, and thrive.
- general: And find satisfaction in doing your part to make the world a better place.
- general: We are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture.
- general: We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.
Travel Requirements
0%
Tags & Categories
Director Infusion Systems
Becton Dickinson
Director Infusion Systems
Job Description
Job Description Summary
Job Description
BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics, and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
We believe that the human element, across our global teams is what allows us to continually evolve. Join us and discover an environment in which you will be supported to learn, grow, and become your best self. Become a maker of possiblewith us.
The Director of Regulatory Affairs reports directly to the Senior Director of Regulatory Affairs. This position is responsible for supporting MMS Infusion products consisting of Medical Devices a along with associated Software and Accessories on a global basis from a Regulatory Affairs standpoint. Support will consist of new product development, sustaining, and end of life activities. The Director will oversee the hiring, training, and career development of their reports.
Responsibilities:
- Lead and develop direct report associates to ensure regulatory compliance
- Problem solve and escalate regulatory and compliance issues to senior management as vital
- Provide effective leadership and team development, effective communication, and quick responses to customers
- Drive continuous improvement in internal processes and customer satisfaction
- Identify, develop, and mentor impactful regulatory talent
- Author and organize regulatory submission content (510(k), Technical Files, etc.)
- Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non-Medical device products and software
- Lead regulatory effort to comply with new and existing regulations (e.g., FDA Medical Device Regulations, EU-MDR)
- Support the monitoring, interpreting, and implementing of current and new regulatory requirements and international standards for U.S., EU., and RoW
- Assure that QMS requirements are followed and executed consistently from RA perspective
- Oversee efforts for Technical File creation and remediation, collaborating with cross-functional teams for required content
- Support regulatory impact assessments for change controls and other RA/QA items from a review and approve level
- Assists in preparing, auditing, editing, and publishing registration documentation, as needed
- Support business export control (BEC) listing of product for release globally per RA requirements
- Support the review and approval of product labeling, promotional, and advertising materials as needed
- Performs other duties and assignments as required
Qualifications:
- Bachelor’s degree in RA, QA, engineering, or other science related discipline
- Advanced degree (e.g. MS, PhD) preferred
- RAPS RAC certification preferred
- Minimum of 10 years of directly related Regulatory Affairs experience in medical devices and/or in vitro diagnostic field
- Minimum of 7 years of personnel management (direct report) experience including performance evaluations/improvement, and career development
- Software experience including SaMD/SiMD is a plus
- Regulatory and Quality Information Management systems such as SAP, RIM, or related systems
- Digital literacy MS Word, Excel, PowerPoint, Teams
- Project Management experience
- Knowledge of global Regulatory Affairs requirements, regulations and standards
- Experience authoring regulatory submissions (US and Global)
- Strong prioritizing, interpersonal, communication, and analytical skills and the ability to multi-task disparate projects
- Ability to represent Regulatory Affairs in multiple environments (e.g. Marketing, R&D, and compliance) and work with all levels of personnel, including VP/GM
- Ability to partner with cross-functional colleagues to identify opportunities for regulatory innovation
- Read, analyze, and interpret regulatory literature and documents and effectively communicate information to peers and management
- Ability to work within a team environment and independently with minimum supervision
- Identify and communicate risks and mitigations associated with global regulatory strategies to cross-functional collaborators and act upon these items appropriately as an RA member
- Demonstrated leadership courage through openness to diverse views, candor in assessing and articulating difficult positions, and willingness to make changes when needed
- Ability to travel globally up to 10% of the time
For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.
Why Join Us?
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
To learn more about BD visit https://bd.com/careers
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
Required Skills
Optional Skills
.
Primary Work Location
USA CA - San Diego TC Bldg C&DAdditional Locations
Work Shift
At BD, we are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates’ progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.
Salary Range Information
$179,200.00 - $322,500.00 USD AnnualLocations
- San Diego, California, United States of America
Salary
180,000 - 280,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- proficiency in MS Word, Excel, PowerPoint, Teamsintermediate
- experience with Regulatory Affairs in medical devices and/or in vitro diagnostic fieldintermediate
- experience with personnel managementintermediate
- experience with Software including SaMD/SiMDintermediate
- experience with Regulatory and Quality Information Management systems such as SAP, RIM, or related systemsintermediate
- experience with Project Managementintermediate
- knowledge of global Regulatory Affairs requirements, regulations and standardsintermediate
- experience authoring regulatory submissions (US and Global)intermediate
- strong prioritizing, interpersonal, communication, and analytical skillsintermediate
- ability to multi-task disparate projectsintermediate
- ability to represent Regulatory Affairs in multiple environmentsintermediate
- ability to partner with cross-functional colleaguesintermediate
- read, analyze, and interpret regulatory literature and documentsintermediate
- effectively communicate information to peers and managementintermediate
- ability to work within a team environment and independently with minimum supervisionintermediate
- identify and communicate risks and mitigationsintermediate
- demonstrated leadership courageintermediate
Required Qualifications
- Bachelor’s degree in RA, QA, engineering, or other science related discipline (degree in ra)
- Advanced degree (e.g. MS, PhD) preferred (degree)
- RAPS RAC certification preferred (certification)
- Minimum of 10 years of directly related Regulatory Affairs experience in medical devices and/or in vitro diagnostic field (experience, 10 years)
- Minimum of 7 years of personnel management (direct report) experience including performance evaluations/improvement, and career development (experience, 7 years)
- Software experience including SaMD/SiMD is a plus (experience)
- Regulatory and Quality Information Management systems such as SAP, RIM, or related systems (experience)
- Digital literacy MS Word, Excel, PowerPoint, Teams (experience)
- Project Management experience (experience)
- Knowledge of global Regulatory Affairs requirements, regulations and standards (experience)
- Experience authoring regulatory submissions (US and Global) (experience)
- Strong prioritizing, interpersonal, communication, and analytical skills and the ability to multi-task disparate projects (experience)
- Ability to represent Regulatory Affairs in multiple environments (e.g. Marketing, R&D, and compliance) and work with all levels of personnel, including VP/GM (experience)
- Ability to partner with cross-functional colleagues to identify opportunities for regulatory innovation (experience)
- Read, analyze, and interpret regulatory literature and documents and effectively communicate information to peers and management (experience)
- Ability to work within a team environment and independently with minimum supervision (experience)
- Identify and communicate risks and mitigations associated with global regulatory strategies to cross-functional collaborators and act upon these items appropriately as an RA member (experience)
- Demonstrated leadership courage through openness to diverse views, candor in assessing and articulating difficult positions, and willingness to make changes when needed (experience)
- Ability to travel globally up to 10% of the time (experience)
Preferred Qualifications
- Advanced degree (e.g. MS, PhD) preferred (degree)
- RAPS RAC certification preferred (certification)
- Software experience including SaMD/SiMD is a plus (experience)
Responsibilities
- Lead and develop direct report associates to ensure regulatory compliance
- Problem solve and escalate regulatory and compliance issues to senior management as vital
- Provide effective leadership and team development, effective communication, and quick responses to customers
- Drive continuous improvement in internal processes and customer satisfaction
- Identify, develop, and mentor impactful regulatory talent
- Author and organize regulatory submission content (510(k), Technical Files, etc.)
- Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non-Medical device products and software
- Lead regulatory effort to comply with new and existing regulations (e.g., FDA Medical Device Regulations, EU-MDR)
- Support the monitoring, interpreting, and implementing of current and new regulatory requirements and international standards for U.S., EU., and RoW
- Assure that QMS requirements are followed and executed consistently from RA perspective
- Oversee efforts for Technical File creation and remediation, collaborating with cross-functional teams for required content
- Support regulatory impact assessments for change controls and other RA/QA items from a review and approve level
- Assists in preparing, auditing, editing, and publishing registration documentation, as needed
- Support business export control (BEC) listing of product for release globally per RA requirements
- Support the review and approval of product labeling, promotional, and advertising materials as needed
- Performs other duties and assignments as required
Benefits
- general: A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work.
- general: It’s also a place where we help each other be great, we do what’s right, we hold each other accountable, and learn and improve every day.
- general: To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
- general: We welcome people with the imagination and drive to help us reinvent the future of health.
- general: At BD, you’ll discover a culture in which you can learn, grow, and thrive.
- general: And find satisfaction in doing your part to make the world a better place.
- general: We are strongly committed to investing in our associates—their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture.
- general: We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.
Travel Requirements
0%
Tags & Categories