Johnson and Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com.
Job Function Regulatory Affairs Group
Job Sub Function Regulatory Affairs
Job Category Professional
All Job Posting Locations Raynham, Massachusetts, United States of America
Job Description At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
About MedTech Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Position Regulatory Affairs Analyst.
Duties / Responsibilities
Project management by maintaining multiple tracking logs for tracking and reporting project status and resource availability
Maintaining compliance pertaining to Medical Device Listings and Establishment Registrations
Effectively initiate, track, and monitor purchase orders and invoices to ensure payments are processed in the company electronic systems in a timely manner
Coordinate logistics for internal and external audits, including on-site and desk audits
Assist with general department responsibilities, such as setting up department meetings, archiving physical and electronic documentation, coordinating regulatory submissions locally and internationally, tracking submission details and metrics, distributing department communication, etc.
Monitor and respond to international requests
Arrange logistics for international visits
Perform other job-related duties as assigned
Qualifications / Requirements
Minimum of a bachelor's degree required. Desired fields of study include science, engineering (e.g., biomedical, electrical, software, mechanical), business, legal, or similar.
Minimum two years of experience in a highly regulated industry, preferably in medical device or pharmaceutical.
Interaction with and support for company executives and department staff
Proficiency of Microsoft Office (Word, Excel, Outlook, PowerPoint, etc.) and other electronic systems
Able to create reports and manipulate data
Strong analytical skills
Flexibility – able to adapt to compliance cycle activities and demanding timelines
Must be well-organized and able to multitask and work with limited supervision
Strong team player
Proactive, taking initiative when needed
Ability to prioritize and seek guidance on prioritization when needed.
Must have excellent written and verbal communication skills, with collaborative attitude and strong attention to detail
Additional Information
The anticipated base pay range for this position is 74,000 to 119,600.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Employees are eligible for the following time off benefits:
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
Caregiver Leave – 10 days
Volunteer Leave – 4 days
Military Spouse Time-Off – 80 hours
Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits
This job posting is anticipated to close on October 25, 2025. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
Pay Transparency 74,000 to 119,600
#J-18808-Ljbffr
Job Function Regulatory Affairs Group
Job Sub Function Regulatory Affairs
Job Category Professional
All Job Posting Locations Raynham, Massachusetts, United States of America
Job Description At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
About MedTech Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech.
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Position Regulatory Affairs Analyst.
Duties / Responsibilities
Project management by maintaining multiple tracking logs for tracking and reporting project status and resource availability
Maintaining compliance pertaining to Medical Device Listings and Establishment Registrations
Effectively initiate, track, and monitor purchase orders and invoices to ensure payments are processed in the company electronic systems in a timely manner
Coordinate logistics for internal and external audits, including on-site and desk audits
Assist with general department responsibilities, such as setting up department meetings, archiving physical and electronic documentation, coordinating regulatory submissions locally and internationally, tracking submission details and metrics, distributing department communication, etc.
Monitor and respond to international requests
Arrange logistics for international visits
Perform other job-related duties as assigned
Qualifications / Requirements
Minimum of a bachelor's degree required. Desired fields of study include science, engineering (e.g., biomedical, electrical, software, mechanical), business, legal, or similar.
Minimum two years of experience in a highly regulated industry, preferably in medical device or pharmaceutical.
Interaction with and support for company executives and department staff
Proficiency of Microsoft Office (Word, Excel, Outlook, PowerPoint, etc.) and other electronic systems
Able to create reports and manipulate data
Strong analytical skills
Flexibility – able to adapt to compliance cycle activities and demanding timelines
Must be well-organized and able to multitask and work with limited supervision
Strong team player
Proactive, taking initiative when needed
Ability to prioritize and seek guidance on prioritization when needed.
Must have excellent written and verbal communication skills, with collaborative attitude and strong attention to detail
Additional Information
The anticipated base pay range for this position is 74,000 to 119,600.
The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year. Bonuses are awarded at the Company's discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company's long-term incentive program.
Employees are eligible for the following time off benefits:
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member
Caregiver Leave – 10 days
Volunteer Leave – 4 days
Military Spouse Time-Off – 80 hours
Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits
This job posting is anticipated to close on October 25, 2025. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
Pay Transparency 74,000 to 119,600
#J-18808-Ljbffr