Abbott Laboratories
Senior Regulatory Affairs Specialist
Abbott Laboratories, Pomona, California, United States, 91768
Senior Regulatory Affairs Specialist
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.JOB DESCRIPTION:
Senior Regulatory Affairs SpecialistWorking at AbbottAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:Career development with an international company where you can grow the career you dream of.Free medical coverage for employees* via the Health Investment Plan (HIP) PPO.An excellent retirement savings plan with high employer contribution.Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.The OpportunityThe position of
Senior Regulatory Affairs Specialist
is within our Toxicology Business Unit located in
Pomona, CA . This role is responsible for directing and coordinating the implementation of regulatory compliance programs as required by federal, state, and local government agencies. This includes achieving government registration and licensure approval of new products and assuring that current products and manufacturing operations are in compliance with applicable regulations. You will interact with Marketing, Sales Regional Regulatory Affairs staff, regional distributors, governmental regulatory agencies, and other third-party accrediting bodies.What You’ll Work OnProvides regulatory support for commercial in-vitro diagnostic products.Performs regulatory assessment for changes made to the on-market products.Understanding of the US 510(k) and EU CE mark (MDR/IVDR) regulatory requirements.Develops regulatory strategies to achieve clearance/approval internationally (outside United States).Compiles and publishes all material required for submissions, license renewals, and annual registrations.Works with governmental regulatory agencies and other third-party accrediting bodies.Maintains approvals/licenses/authorizations for existing marketing authorizations.Adds and maintains information contained in the Global Regulatory Information Database.Provides recommendations on labeling, for regulatory compliance.Develops internal procedures and tools.Conducts informational or training sessions for stakeholders.Organizes and maintains hard copy and electronic department files.Keeps informed of global regulatory information.Carries out duties in compliance with established business policies.Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.Demonstrates commitment to the development, implementation, and effectiveness of Company Quality Management System per ISO, FDA, and other regulatory agencies.Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing, and testing activities.Performs other duties and projects as assigned.Required QualificationBachelor’s degree (BS/BA) in a scientific field.3-5 years of experience in a regulated industry.Proficient with Microsoft Office, including Word, Excel, PowerPoint, and Visio.Able to work on multiple tasks as a team member and/or ability to operate as an individual contributor.Must be detail-oriented, self-motivated and available for flexible scheduling.Strong written and verbal communication, problem-solving, and motivational skills.Preferred Qualification3 years of experience in Regulatory Affairs.Three plus years in an IVD or medical device manufacturing environment.510k submission experience.Technical file creation and maintenance experience.Strong knowledge of US and Foreign regulations.Able to work on multiple tasks simultaneously as a team member and/or ability to operate as an individual contributor.Possess a high degree of accuracy, detail-oriented, self-motivated, and available for flexible scheduling.Apply Now* 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.Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.The base pay for this position is
$83,600.00 – $167,200.00. In specific locations, the pay range may vary from the range posted.JOB FAMILY:
Regulatory OperationsDIVISION:
TOX ARDx ToxicologyLOCATION:
United States > Pomona: 829 Towne Center DriveWORK SHIFT:
StandardTRAVEL:
Not specifiedMEDICAL SURVEILLANCE:
Not ApplicableSIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8-hour day), Keyboard use (greater or equal to 50% of the workday).Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
#J-18808-Ljbffr
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.JOB DESCRIPTION:
Senior Regulatory Affairs SpecialistWorking at AbbottAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:Career development with an international company where you can grow the career you dream of.Free medical coverage for employees* via the Health Investment Plan (HIP) PPO.An excellent retirement savings plan with high employer contribution.Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.The OpportunityThe position of
Senior Regulatory Affairs Specialist
is within our Toxicology Business Unit located in
Pomona, CA . This role is responsible for directing and coordinating the implementation of regulatory compliance programs as required by federal, state, and local government agencies. This includes achieving government registration and licensure approval of new products and assuring that current products and manufacturing operations are in compliance with applicable regulations. You will interact with Marketing, Sales Regional Regulatory Affairs staff, regional distributors, governmental regulatory agencies, and other third-party accrediting bodies.What You’ll Work OnProvides regulatory support for commercial in-vitro diagnostic products.Performs regulatory assessment for changes made to the on-market products.Understanding of the US 510(k) and EU CE mark (MDR/IVDR) regulatory requirements.Develops regulatory strategies to achieve clearance/approval internationally (outside United States).Compiles and publishes all material required for submissions, license renewals, and annual registrations.Works with governmental regulatory agencies and other third-party accrediting bodies.Maintains approvals/licenses/authorizations for existing marketing authorizations.Adds and maintains information contained in the Global Regulatory Information Database.Provides recommendations on labeling, for regulatory compliance.Develops internal procedures and tools.Conducts informational or training sessions for stakeholders.Organizes and maintains hard copy and electronic department files.Keeps informed of global regulatory information.Carries out duties in compliance with established business policies.Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.Demonstrates commitment to the development, implementation, and effectiveness of Company Quality Management System per ISO, FDA, and other regulatory agencies.Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing, and testing activities.Performs other duties and projects as assigned.Required QualificationBachelor’s degree (BS/BA) in a scientific field.3-5 years of experience in a regulated industry.Proficient with Microsoft Office, including Word, Excel, PowerPoint, and Visio.Able to work on multiple tasks as a team member and/or ability to operate as an individual contributor.Must be detail-oriented, self-motivated and available for flexible scheduling.Strong written and verbal communication, problem-solving, and motivational skills.Preferred Qualification3 years of experience in Regulatory Affairs.Three plus years in an IVD or medical device manufacturing environment.510k submission experience.Technical file creation and maintenance experience.Strong knowledge of US and Foreign regulations.Able to work on multiple tasks simultaneously as a team member and/or ability to operate as an individual contributor.Possess a high degree of accuracy, detail-oriented, self-motivated, and available for flexible scheduling.Apply Now* 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.Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.The base pay for this position is
$83,600.00 – $167,200.00. In specific locations, the pay range may vary from the range posted.JOB FAMILY:
Regulatory OperationsDIVISION:
TOX ARDx ToxicologyLOCATION:
United States > Pomona: 829 Towne Center DriveWORK SHIFT:
StandardTRAVEL:
Not specifiedMEDICAL SURVEILLANCE:
Not ApplicableSIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8-hour day), Keyboard use (greater or equal to 50% of the workday).Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
#J-18808-Ljbffr