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Johnson & Johnson is hiring a Senior Manager / Associate Director for the Solids Development (SOliD) team in Beerse, Belgium. You will lead formulation and process development for solid drug products, manage transfers, and drive regulatory submissions with a cross-functional mindset.
You will mentor staff, plan resources, and coordinate with Regulatory, Analytical Development, and Manufacturing to ensure alignment with CMC goals, while upholding GMP, safety and quality standards in a dynamic,
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 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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmaceutical Product R&D
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We\'re hiring a Senior Manager / Associate Director into our Solids Development (SOliD) department within Drug Product Research & Development in Beerse, Belgium. We\'d love to hear from you!
In SoliD, we design every solid formulation and process across the Janssen R&D Synthetics portfolio, from late Discovery through Commercialization.
Advance formulation and process development for synthetic molecules. Explore new drug delivery systems and technologies, create patient-centric products and fresh IP. Run technology transfers. Deliver regulatory submissions. Guide several programs at once and keep them aligned to CMC objectives and timelines. Apply Best Product at Pivotal and Speed to the Clinic principles. Plan resources, set priorities and decide what comes first when programs overlap. Uphold quality, compliance and safety, and know the rules that apply — GMP included, along with Safety, Health and Environment. Help shape our direction from the SoliD Leadership Team.
Recruit dedicated scientists and Mentor them. Lead your team to solve bigger problems each year. Connect SoliD with Pharmaceutical & Material Sciences, Analytical Development, Pharmaceutical Supply & Engineering Sciences, Supply Chain, Quality and Regulatory. Partner with academia and CDMOs to deliver on your projects.
Preferred Skills:
Budget Management, Chemistry, Manufacturing, and Control (CMC), Clinical Trial Protocols, Data Governance, Developing Others, Drug Discovery Development, Inclusive Leadership, Industry Analysis, Interdisciplinary Work, Leadership, Market Research, Process Improvements, Product Development, Product Strategies, Prototype Development, Researching, Scientific Research, Team Management
The anticipated base pay range for this position is:
€96.000,00 - €165.025,00
Benefits:
In addition to base pay, we offer the following benefits*:
*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.
For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.