Senior Scientist CMC Regulatory Affairs

• Job title Senior Scientist CMC Regulatory Affairs
• Function Discovery & Pre-Clinical/Clinical Development
• Sub function Regulatory Science
• Category Senior Scientist, Regulatory Science (ST6)
• Location Spring House / Cambridge / Raritan / Titusville / Wayne / Horsham / Malvern / United States of America
• Date posted Jul 07 2025
• Requisition number R-022395
• Work pattern Hybrid Work

This job posting is anticipated to close on Jul 28 2025. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.

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

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Regulatory Science

Job Category:

Scientific/Technology

All Job Posting Locations:

Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, Malvern, 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, Wayne, Pennsylvania, 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

We are currently seeking a motivated Senior Scientist in CMC Regulatory Affairs to join our dynamic team. This role can be based our East Coast USA locations.

Please 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):

Beerse, Belgium - R-021616

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

Position Summary:

The successful candidate will play a critical role in supporting a broad range of regulatory activities within the Chemistry, Manufacturing, and Controls (CMC) area of Global Regulatory Affairs. This position will involve collaboration with various professional colleagues, including CMC/Supply Chain team members, Therapeutic Area Leaders, and GRA management.

Main Duties and Key Responsibilities:

• Support the alignment of CMC regulatory strategy with global/regional/commercial regulatory objectives.
• Collaborate with senior level CMC RA colleagues to ensure connectivity to overall global regulatory strategy.
• Develop CMC content and dossier plans under the supervision of senior CMC RA personnel.
• Assist in the preparation of global dossiers and variations for submission to Health Authorities.
• Manage CMC submissions for renewals, annual product submissions, and inquiries from local partners and health authorities.
• Coordinate and compile CMC country-specific documents required for global submission approvals.
• Oversee the global submission plan and timeline.
• Contribute to the implementation of global CMC regulatory strategies and dossier plans through collaboration with CMC RA teams.
• Prepare responses to Health Authority questions or communications in line with global product strategy.
• Alert CMC Regulatory Affairs Management to issues affecting registration, compliance, and product lifecycle management.
• Track submission-related activities across all necessary CMC RA systems.

Leadership Competencies:

The Senior Scientist in Regulatory Affairs should:

• Proactively identify and respond to problems and opportunities.
• Consistently deliver results that meet or exceed expectations, focusing on driving customer value.
• Make decisions based on factual evidence.
• Challenge the status quo to find more efficient and effective ways of working.

Qualifications:

• University degree in engineering, biological, pharmaceutical, or chemical sciences with a minimum of 3 years of relevant experience (preferred), which may include post-graduate education and/or experience in the pharmaceutical or healthcare industry.
• Prior experience in drug development, analytical development, or manufacturing is preferred, with a solid understanding of biology, chemistry, and/or engineering. Regulatory experience in this area is encouraged.
• Familiarity with global CMC regulatory procedures and guidelines.
• Experience working in project teams and/or matrix organizations.
• Excellent oral and written communication skills.
• Ability to thrive in a collaborative team environment as an individual contributor.
• Proficient in spoken and written English.

The anticipated base pay range for this position is :

$105,000 to $169,050

Additional Description for Pay Transparency:

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 - up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year Holiday pay, including Floating Holidays - up to 13 days per calendar year of Work, Personal and Family Time - up to 40 hours per calendar year Additional information can be found through the link below. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.