This listing was posted on Professional Diversity Network.
Staff Regulatory Affairs Specialist - Hybrid
Location:
Franklin Lakes, NJ
Description:
Responsibilities Job Description Summary The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product development. The incumbent will represent the RA function on designated platform core team implementing regulatory strategies to support cross-functional stand-alone medical device and combination product development efforts for platform growth and global expansion. This is an excellent opportunity to lead and gain hand on experience in regulatory field with Business-to-Business customer exposure, US, EU and global submission activity, regulatory intelligence reviews, health authority interactions/audits, and project management.The ideal candidate will have medical device and drug-device combination product experience in the US and EU. The role may have 1-2 indirect reports. This position will work on site Hybrid in Franklin Lakes, NJ three days per week. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.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'll be supported to learn, grow and become your best self. Become a maker of possible with us. Responsibilities Acts as a RA Core team Member (RA CTM) and works with RA Manager and Platform Leaders to ensure timely execution of regulatory strategies with business objectives and customer resultsAssesses regulatory pathways for new products, product modifications or product conversions; develops regulatory strategies and planning for submissions or support of customers' regulatory submissionsAuthoring and maintenance of compliant regulatory files and supporting documentation (510k/ US master files/EUMDR technical files)Partners with and supports Pharma customers in securing timely development, submissions, addressing health authority questions and regulatory drug-device combination products approvalsPerforms regulatory impact assessment of changes linked to the field of expertise and assigned platformLiaises with cross-functional and cross company teams to meet customer needs in driving new global marketsDevelops and maintains knowledge & awareness on assigned fields of expertise: identify applicable regulations and standards, perform regulatory intelligence/watch, educate appropriate contact partnersIdentifies and communicates potential risks and mitigations to partnersSupport to customers for regulatory advice and registration of their products and interact as needed with the U.S. FDA and EU Notified BodiesReviews and/or approves product marketing claims and communication, Advertising/promotional materials, and labelingConduct trainings on regulatory issues for staff and for business customers (e.g., Platform, R&D, Marketing and Pharma Partners)Participates in internal/external trade, professional, and standards development organizationsLeads multiple projects with minimal direction About you: To be successful in this role, you require:Knowledge in pharmaceutical and medical devices regulation registration requirements and pathways (variations, renewals, supplements), in the US and EU markets. Global experience is a plus.Understanding of new product development cycle, clinical phases, organizational change and quality management systems complianceExperience with Eletromechanical devices. Knowledge of SaMD and drug delivery devices (on-body injector, pumps, pen injector, auto-injector) and pre-fillable syringes is preferred.Experience in meeting with, making presentations to, and negotiating with senior leadership and/or health authoritiesAbility to use your time productively and efficiently (structured and self-organized with strong project management skills)Ability to resolve problems and to make appropriate regulatory decisions under pressureAbility to adapt, multitask and respond quickly in a constantly evolving and often unique, ambiguous environment, Strong team player.Ability to drive and maintain favorable customer experience and customer-centricity (internal & external) Education and experience required: Minimum: B.S. or B.A. degree in a technical field (e.g., engineering, biology, chemistry). Advanced degree preferred.Professional Certification (s) is preferred (RAPS-RAC, PMP, ASQ etc)Minimum five years of directly related professional experience (Regulatory) in increasingly responsible positions in the medical device, biologic, or pharmaceutical fieldsProven experience with project management, negotiation, influencing and interpersonal skills.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.PDN Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift NA (United States of America) Apply Save Job Responsibilities Job Description Summary The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at the project level in developing and executing regulatory strategy and compliance plans to promote and support drug delivery solutions for pharma combination product development. The incumbent will represent the RA function on designated platform core team implementing regulatory strategies to support cross-functional stand-alone medical device and combination product development efforts for platform growth and global expansion. This is an excellent opportunity to lead and gain hand on experience in regulatory field with Business-to-Business customer exposure, US, EU and global submission activity, regulatory intelligence reviews, health authority interactions/audits, and project management.The ideal candidate will have medical device and drug-device combination product experience in the US and EU. The role may have 1-2 indirect reports. This position will work on site Hybrid in Franklin Lakes, NJ three days per week. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.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'll be supported to learn, grow and become your best self. Become a maker of possible with us. Responsibilities Acts as a RA Core team Member (RA CTM) and works with RA Manager and Platform Leaders to ensure timely execution of regulatory strategies with business objectives and customer resultsAssesses regulatory pathways for new products, product modifications or product conversions; develops regulatory strategies and planning for submissions or support of customers' regulatory submissionsAuthoring and maintenance of compliant regulatory files and supporting documentation (510k/ US master files/EUMDR technical files)Partners with and supports Pharma customers in securing timely development, submissions, addressing health authority questions and regulatory drug-device combination products approvalsPerforms regulatory impact assessment of changes linked to the field of expertise and assigned platformLiaises with cross-functional and cross company teams to meet customer needs in driving new global marketsDevelops and maintains knowledge & awareness on assigned fields of expertise: identify applicable regulations and standards, perform regulatory intelligence/watch, educate appropriate contact partnersIdentifies and communicates potential risks and mitigations to partnersSupport to customers for regulatory advice and registration of their products and interact as needed with the U.S. FDA and EU Notified BodiesReviews and/or approves product marketing claims and communication, Advertising/promotional materials, and labelingConduct trainings on regulatory issues for staff and for business customers (e.g., Platform, R&D, Marketing and Pharma Partners)Participates in internal/external trade, professional, and standards development organizationsLeads multiple projects with minimal direction About you: To be successful in this role, you require:Knowledge in pharmaceutical and medical devices regulation registration requirements and pathways (variations, renewals, supplements), in the US and EU markets. Global experience is a plus.Understanding of new product development cycle, clinical phases, organizational change and quality management systems complianceExperience with Eletromechanical devices. Knowledge of SaMD and drug delivery devices (on-body injector, pumps, pen injector, auto-injector) and pre-fillable syringes is preferred.Experience in meeting with, making presentations to, and negotiating with senior leadership and/or health authoritiesAbility to use your time productively and efficiently (structured and self-organized with strong project management skills)Ability to resolve problems and to make appropriate regulatory decisions under pressureAbility to adapt, multitask and respond quickly in a constantly evolving and often unique, ambiguous environment, Strong team player.Ability to drive and maintain favorable customer experience and customer-centricity (internal & external) Education and experience required: Minimum: B.S. or B.A. degree in a technical field (e.g., engineering, biology, chemistry). Advanced degree preferred.Professional Certification (s) is preferred (RAPS-RAC, PMP, ASQ etc)Minimum five years of directly related professional experience (Regulatory) in increasingly responsible positions in the medical device, biologic, or pharmaceutical fieldsProven experience with project management, negotiation, influencing and interpersonal skills.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.PDN Primary Work Location USA NJ - Franklin Lakes Additional Locations Work Shift NA (United States of America) Apply Save Job PDN-9b9d16a0-6ffb-4b8a-a348-c9fc3b2fa071
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More About this Listing: Staff Regulatory Affairs Specialist - Hybrid
Staff Regulatory Affairs Specialist - Hybrid is a Other Jobs Regulatory Affairs Specialist Job at Becton Dickinson located in Franklin Lakes NJ. Find other listings like Staff Regulatory Affairs Specialist - Hybrid by searching Oodle for Other Jobs Regulatory Affairs Specialist Jobs.
Staff Regulatory Affairs Specialist - Hybrid is a Other Jobs Regulatory Affairs Specialist Job at Becton Dickinson located in Franklin Lakes NJ. Find other listings like Staff Regulatory Affairs Specialist - Hybrid by searching Oodle for Other Jobs Regulatory Affairs Specialist Jobs.