Abbott Laboratories
Regulatory Affairs Manager
Abbott Laboratories, Austin, Texas, us, 78716
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.Our Neuromodulation business is an area of expertise for Abbott. This business includes implantable devices compatible with mobile technology to help people who suffer from chronic pain and movement disorders. Our Solutions include Proclaim (TM) XR SCS System, the #1 Spinal cord stimulator on the market, Proclaim (TM) DRG Neurostimulator, the only FDA approved DRG therapy and a market leader in radiofrequency ablation therapy, Abbott RFA. These non-opioid therapies allow us to provide interventional pain therapy to patients throughout the pain continuum. Our deep brain stimulation technology for progressive diseases help people manage their Parkinson’s disease and essential tremor symptoms, steering away from side effects.Our Plano or Austin, Texas locations, currently have an opportunity for a
Regulatory Affairs Manager . This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. This new team member will apply advanced regulatory expertise to guide cross-functional partners and demonstrate strategic thinking and creativity in support of programs.WHAT YOU’LL DODevelops sound global regulatory strategies for new and modified medical devicesPrepares robust regulatory applications to achieve departmental and organizational objectivesCreates, reviews and approves engineering changesProvides leadership and guidance (including training) to other members of the RA staff as well as to cross-functional team members and development teamsReviews device labeling and marketing materials for compliance with FDA submissions and applicable regulationsProvides global strategic input to development teams (including all feasible alternatives and associated risks)Drives cross functional alignment with issues that could have Regulatory ramificationsIndependently interacts and builds partnerships with competent authorities (FDA, and other regulatory agencies)Builds strategic partnerships to further departmental and organizational objectivesReviews of product and manufacturing changes for compliance with applicable regulations (Change Control)Reviews protocols and reports to support regulatory submissionsAssesses proposed regulations and communicates new requirements to the organizationSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirementsComplies with U.S. Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignmentsMaintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendorsAssists with audits and inspections, if required.Performs other related duties and responsibilities, on occasion, as assignedEDUCATION AND EXPERIENCE YOU’LL BRINGRequired:Bachelor’s Degree OR an equivalent combination of education and experience8+ years technical experience6+ years medical device regulatory experience. Extensive experience with US and global medical device regulations and submissions.Ability to work in a highly matrixed and geographically diverse business environment.Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results.Ability to work effectively within a team in a fast-paced changing environment.Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.Multi-tasks, prioritizes and meets deadlines in timely manner.Strong organizational, planning, and follow-up skills and ability to hold others accountable.Preferred
:Bachelor’s degree in technical disciplineExperience working in a broader enterprise/cross division business unit modelExperience with 510(k) applications, IDEs, PMA or PMA supplements and US device regulations and/or experience with EU and other international medical device regulations and submissionsExperience acting as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development teamExperience acting as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detailExperience supporting audits by regulatory agencies, including GMP, ISO13485, and FQA auditsExperience creating intradepartmental proceduresExperience leading or supervising a teamWHAT WE OFFERAt Abbott, you can have a good job that can grow into a great career. We offer:Training and career development
, with onboarding programs for new employees and tuition
assistanceFinancial security
through competitive compensation, incentives and retirement plansHealth care and well-being programs
including medical, dental, vision, wellness and occupational health programs.
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.Paid time off401(k)
retirement savings with a generous company matchThe stability of a company
with a record of strong financial performance and history of being actively involved in local communitiesLearn more about our benefits that add real value to your life to help you live fully:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at
www.abbott.com
, on Facebook at
www.facebook.com/Abbott
and on Twitter @AbbottNews and @AbbottGlobal
The base pay for this position is $95,000.00 – $190,000.00. In specific locations, the pay range may vary from the range posted.
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Regulatory Affairs Manager . This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. This new team member will apply advanced regulatory expertise to guide cross-functional partners and demonstrate strategic thinking and creativity in support of programs.WHAT YOU’LL DODevelops sound global regulatory strategies for new and modified medical devicesPrepares robust regulatory applications to achieve departmental and organizational objectivesCreates, reviews and approves engineering changesProvides leadership and guidance (including training) to other members of the RA staff as well as to cross-functional team members and development teamsReviews device labeling and marketing materials for compliance with FDA submissions and applicable regulationsProvides global strategic input to development teams (including all feasible alternatives and associated risks)Drives cross functional alignment with issues that could have Regulatory ramificationsIndependently interacts and builds partnerships with competent authorities (FDA, and other regulatory agencies)Builds strategic partnerships to further departmental and organizational objectivesReviews of product and manufacturing changes for compliance with applicable regulations (Change Control)Reviews protocols and reports to support regulatory submissionsAssesses proposed regulations and communicates new requirements to the organizationSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirementsComplies with U.S. Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignmentsMaintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendorsAssists with audits and inspections, if required.Performs other related duties and responsibilities, on occasion, as assignedEDUCATION AND EXPERIENCE YOU’LL BRINGRequired:Bachelor’s Degree OR an equivalent combination of education and experience8+ years technical experience6+ years medical device regulatory experience. Extensive experience with US and global medical device regulations and submissions.Ability to work in a highly matrixed and geographically diverse business environment.Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results.Ability to work effectively within a team in a fast-paced changing environment.Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.Multi-tasks, prioritizes and meets deadlines in timely manner.Strong organizational, planning, and follow-up skills and ability to hold others accountable.Preferred
:Bachelor’s degree in technical disciplineExperience working in a broader enterprise/cross division business unit modelExperience with 510(k) applications, IDEs, PMA or PMA supplements and US device regulations and/or experience with EU and other international medical device regulations and submissionsExperience acting as a regulatory representative on core product development teams, communicates regulatory requirements and impact of regulations to the development teamExperience acting as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detailExperience supporting audits by regulatory agencies, including GMP, ISO13485, and FQA auditsExperience creating intradepartmental proceduresExperience leading or supervising a teamWHAT WE OFFERAt Abbott, you can have a good job that can grow into a great career. We offer:Training and career development
, with onboarding programs for new employees and tuition
assistanceFinancial security
through competitive compensation, incentives and retirement plansHealth care and well-being programs
including medical, dental, vision, wellness and occupational health programs.
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.Paid time off401(k)
retirement savings with a generous company matchThe stability of a company
with a record of strong financial performance and history of being actively involved in local communitiesLearn more about our benefits that add real value to your life to help you live fully:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at
www.abbott.com
, on Facebook at
www.facebook.com/Abbott
and on Twitter @AbbottNews and @AbbottGlobal
The base pay for this position is $95,000.00 – $190,000.00. In specific locations, the pay range may vary from the range posted.
#J-18808-Ljbffr