Experienced Scientist, CMC Regulatory Science

Antwerp - Belgium

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

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:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Regulatory Science

Job Category:

Scientific/Technology

All Job Posting Locations:

Beerse Antwerp Belgium

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 Summary:

The Experienced Scientist Regulatory:

is responsible for supporting team members for a broad range of regulatory activities in the Chemistry Manufacturing and Controls area of Global Regulatory Affairs.
may interact with professional colleagues including the CMC/Supply Chain team members Therapeutic Area Leaders and GRA management as project and functional objectives and needs dictate.
works with other CMC RA personnel to manage and resolve any issues.

Main duties and responsibilities:

The Experienced Scientist Regulatory:

assists in ensuring the CMC regulatory strategy is in alignment with the global/regional/commercial regulatory strategy. Further assures connectivity and alignment to the overall global regulatory strategy through partnership with other senior level CMC RA personnel.
Under the supervision/collaboration of more senior CMC RA personnel
develops CMC content and dossier plans
assists in the preparation of global dossiers/variations for submission to Health Authorities
assists with CMC submissions for renewals annual product submissions and questions from LOC partners/health authorities/other J&J partners
coordinates compiles and manages CMC country specific documents required as part of the approval process for global submissions
executes the oversight of the global submission plan and timing
contributes to the implementation of global CMC regulatory strategies and dossier plans by collaborating with other CMC RA personnel
assists in preparing responses to HA questions or other HA communications in alignment with the global product strategy
Escalates issues to CMC Regulatory Affairs Management that affect registration regulatory compliance and continued lifecycle management of the product.
Manages the inputs/tracking for submission related activities in all required CMC RA systems
Contributes to the implementation of the global CMC regulatory strategies

Leadership Competencies:

The Experienced Scientist Regulatory:

Proactively senses and responds to problems and opportunities
Consistently delivers results that meet or exceed expectations; keeps the focus on driving customer value
Makes decisions based on facts
Challenges the status quo to identify ways of doing things better and more efficiently

Education and Experience:

University degree in engineering biological pharmaceutical or chemical sciences with generally a minimum of 1 year of experience (preferred) inclusive of post graduate education and/or pharmaceutical or health care industry experience
Prior experience in drug development analytical development or manufacturing preferred with solid understanding of biology chemistry and/or engineering. Regulatory experience within this scope encouraged
Experience with global CMC regulatory procedures and guidelines/requirements
Experience in working in project teams and/or a matrix organization
Excellent oral and written communication skills.
The ability to work successfully within a collaborative team environment as an individual contributor

Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow 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).

Allschwil Switzerland - Requisition Number: R-070627

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

Required Skills:

Preferred Skills:

Required Experience:

Senior IC

Apply Now

About Company

Johnson & Johnson

About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more

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