Manager, Safety Analysis Scientist

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Product Safety

Job Sub Function:

Product Safety Risk Management

Job Category:

Scientific/Technology

All Job Posting Locations:

Horsham Pennsylvania United States of America Raritan New Jersey United States of America Spring House Pennsylvania United States of America Titusville New Jersey United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at Oncology

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures. We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings we recommend focusing on the specific country(s) that align with your preferred location(s):

United Kingdom- Requisition Number: R-081594

Remember whether you apply to one or all of these requisition numbers your applications will be considered as a single submission.

We are searching for the best talent for a Manager Safety Analysis Scientist located in Raritan NJ; Titusville NJ; Spring House PA; or Horsham PA. This is a hybrid position that requires you to be on site three days a week.

Purpose:

The Manager Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products. The Manager SAS in partnership with the Medical Safety Officer (MSO) is responsible for the preparation of scientific safety analysis and evaluations which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.

The Manager SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a products safety strategy complete safety analyses and evaluations proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation supporting SMT deliverables as required.

The Manager SAS will assist the MSO with activities related to the SMT and with contributions to key safety and clinical documents.

The Manager SAS will have in-depth product knowledge will serve as product point of contact and will provide mentoring to and oversight of deliverables prepared by other team members as needed (for complex reports).

The Manager SAS will function independently or with moderate guidance from the Director SAS Therapeutic Area Lead (TAL) be able to link discussions to content and deliver quality results with minimal guidance. The Manager SAS will build alliances and be able to influence other safety partners to shape decisions/outcomes.

You will be responsible for:

• Lead safety evaluations including strategy discussions collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary data retrieval data analysis report writing and report revision.
• Ensure high quality safety evaluations and reports with minimal-to-moderate comments from stakeholders and minimal-to-moderate revisions required.
• Provide support to AD SASs for novel projects without defined processes.
• Provide input and review to key regulatory or clinical documents as appropriate.
• Demonstrate leadership in the SMT and support the MSO.
• Support SMT activities (e.g. preparing and presenting data compiling meeting minutes updating signal tracking information).
• Lead proactive safety data reviews if applicable and form a safety position across GMS which can be leveraged for aggregate safety reports.
• Provide support for Health Authority interactions regarding safety and risk management both written and verbal.
• Contribute to cross-functional training of relevant stakeholders.
• Mentor other SASs on activities within the role.
• Participate in department and/or cross-functional initiatives and explore innovative ways of presenting data preparing reports and improving efficiencies.
• Assist in the creation review and implementation of controlled documents and other related tools.
• Support audits/inspections.

Qualifications / Requirements:

Education:

• Bachelors Degree Required: Healthcare-related or Biomedical Science (9 years of industry experience or equivalent).
• Advanced Degree Preferred: Healthcare-related or Biomedical Science (6 years industry experience or equivalent).

Experience:

Required:

• Working knowledge of medical concepts and familiarity with safety activities in drug development and post marketing and global safety health authority requirements.
• Medical writing or PV experience.
• Ability to understand and analyze complex medical-scientific data from a broad range of sources.
• Ability to interpret and present complex data to determine benefit-risk impact.
• Excellent English verbal and written communication skills.
• Ability to effectively interact with stakeholders including business partners.
• Ability to work in a matrix environment proven leadership skills.
• Ability to plan work to meet deadlines and effectively handle multiple priorities.
• Proficiency in Microsoft applications (e.g. Word Excel and PowerPoint).
• Ability to influence negotiate and communicate with both internal and external customers.

Preferred:

• Clinical experience.

The anticipated base pay range for this position in the US is $117000 - $201250. The anticipated base pay range for the Bay Area is $133000 - $230000.

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 corporations performance over a calendar/performance year. Bonuses are awarded at the Companys discretion on an individual basis.

Subject to the terms of their respective plans employees and/or eligible dependents are 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.

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).

This position is eligible to participate in the Companys long-term incentive program.

Subject to the terms of their respective policies and date of hire Employees are eligible for the following time off benefits:

• Vacation - 120 hours per calendar year
• Sick time - 40 hours per calendar year; for employees who reside in the State of Washington - 56 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

For additional general information on Company benefits please go to:

more information on how we support the whole health of our employees throughout their wellness career and life journey please visit .

This job posting is anticipated to close on June 15th 2026 The Company may however extend this time-period in which case the posting will remain available on 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 external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Required Skills:

Preferred Skills:

Business Alignment Clinical Operations Coaching Compliance Management Compliance Risk Critical Thinking Data Reporting Medicines and Device Development and Regulation Organizing Quality Control (QC) Research Ethics Researching Risk Management Safety Investigations Safety-Oriented Serious Adverse Event Reporting Standard Operating Procedure (SOP) Technical Writing