Sr. RA professional- Global Regulatory Scientist

Janssen-Cilag Limited; Leiden; On-site; EUR 66,000 - 105,000; Full time

Benefits offered by this job

Annual bonus

Comprehensive benefits

Travel opportunities

Job summary

Johnson & Johnson Innovative Medicine is seeking a Sr. Regulatory Scientist to support global regulatory submissions for interventional oncology products.

The role involves coordinating IND/CTA/NDA/MAA filings, advising on documentation strategies, and aligning with local operating companies to meet submission timelines. The successful candidate will bring broad regulatory experience across product types, strong collaboration skills, and a track record in regulatory strategy and life cycle

Qualifications

• Bachelor’s Degree in a scientific subject with 6 years of industry experience or Master’s with 4 years of experience, or PharmD/PhD with 2 years of experience.
• Experience across product types (pharma, devices, combo products) preferred.
• Solid understanding of FDA and ICH regulatory requirements and guidelines for clinical research and life cycle submissions.

Responsibilities

• Prepare and support regulatory submissions (IND, CTA, NDA/MAA, eCTD).
• Advise on documents and strategies for NDA/MAA and other global filings.
• Support marketing authorization submissions and ensure timely document readiness.
• Liaise with LOCs and coordinate responses to health authorities.
• Participate in global regulatory team meetings and strategy development.

Skills

Regulatory submissions

Global regulation knowledge

Cross-functional collaboration

Regulatory strategy

Project management

Education

Bachelor's degree in science

Master's degree in a related field

PharmD/PhD with 2 years experience

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com .

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:
Regulatory Affairs Group

Job Sub Function:
Regulatory Product Submissions and Registration

Job Category:
Professional

All Job Posting Locations:
Leiden, Netherlands

Job Description:

Johnson & Johnson Innovative Medicine is recruiting for Sr. RA professional- Global Regulatory Scientist , Regulatory Affairs to support the initiatives for the Interventional Oncology group (INTO). The position focuses on novel interventional oncology products, including combination products and platforms with limited regulatory precedent, designed to deliver therapies directly into the tumor. Preferred location: EU – Netherlands

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 https://www.jnj.com/innovative-medicine

Johnson & Johnson Innovative Medicine R&D is recruiting for

Sr. RA professional - Global Regulatory Scientist, Regulatory Affairs (PG 26)

Key Responsibilities:

Under the direction of the GRL, Regional Regulatory Leader (RRL), your key responsibilities include the following:

• - Draft cover letters and support the preparation of various applications ie: IND, CTA, MAA/NDA and eCTD), and procedures for Regulatory Agency submissions
• - For CTA/INDs – Ensure protocols are in alignment with regulatory requirements and provide advice on required documents and submission strategies in preparation for those filings.
• - For Marketing Authorization Applications (NDA, MAA or other major HA submissions): Provide regulatory support throughout registration process
• - Advise team on required documents and submission strategies in preparation of NDA, MAA (and other global filings) as assigned (in collaboration with LOCs as appropriate)
• - Assist with timely NDA, MAA (other) document availability, ensure that all document components are in place on time, identify and track critical path activities
• - Assist with submission and acceptance of Marketing Authorization Applications (NDA, MAA, other)
• - Ensure country-specific submission packages are made available to the LOCs in accordance with agreed plans
• - Assist in the preparation of meetings with Regulatory Agencies. Coordinate, contribute to development, and review the content of responses to queries from HAs to ensure high quality and timely responses. May include other activities as delegated by the RRL/GRL.
• - Liaise with Local Operating Companies (LOCs), track dates of submissions/responses to queries in a timely manner.
• - Acts as back up contact/representative on specific multi-discipline teams, or with regulatory agencies as needed. May be responsible for organizing and leading meetings.
• - Provide regulatory input for and appropriate follow-up to inspections, audits, litigation support, and product complaints.
• - Supports GRL(GRT) by driving high project management planning of global submissions or Health authority interactions and additional major regulatory milestones.
• - Participate in global regulatory team meetings as appropriate
• - Assist in strategy development by researching regulatory and medical information in preparing submissions to Global Health Authorities (HAs).
• - Advise the Regulatory team on applicable regulatory requirements, project specific regulatory issues as assigned
• - Partner with regulatory colleagues understand the competitive landscape, e.g., views of HAs, regulatory precedents, labeling differences, and disease area-specific issues.
• - May assist in the development and improvement of regulatory processes.

Qualifications Experience and Skills:

• - Bachelor’s Degree in a scientific or equivalent subject area with 6 years of relevant industry experience or Master’s degree with 4 years of relevant experience, or PharmD/Ph.D. with 2 years of relevant experience is required.
• - experience in flexing across different product types (pharma, devices, combo products) preferred.
• - Knowledge of multiple global health authorities ‘regulations and processes’ would be ideal
• - Solid understanding of FDA and ICH Regulatory requirements and guidelines specific to the areas of clinical research, product development, life cycle submission management and product labeling is required.
• - Therapeutic area experience in oncology is beneficial. Experience with, combination products (drug and devices), would be an asset
• - Intellectual curiosity and an ability/flexibility in learning new things and working in novel areas with limited regulatory precedence. This role will include an opportunity to flex across different product types (pharma, devices, combo products).
• - Experience preparing responses to health authorities, managing Health Authorities interactions, and life cycle management of clinical trials and marketing authorizations submissions (ie: IND/CTAS/NDA/BLA, MAAS other)
• - Experience in strategic planning, technical data summary and cross functional management is required

Leadership Capabilities

• - Strong organizational and time management skills.
• - Strong collaboration skills, including effective communication and conflict resolution skills.
• - Strong capabilities and ability to work successfully in a matrixed environment.
• - Effective critical thinking, including problem solving and goal setting.
• - Demonstrated ability to think strategically and contingency plan in order to meet business objectives.
• - 10% domestic travel and potential international travel will be required for this position.

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is:
€66,000.00 - €105,110.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.