Sr Scientist Pharma Prod RD, Dry Granulation

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

Job Function:

Job Sub Function:

Job Category:

All Job Posting Locations:

Job Description:

The Global Pharmaceutical Product Development and Supply (PPDS) organization part of the Discovery Product Development and Supply (DPDS) division of JJIM is dedicated to developing advanced drug delivery solutions. Within PPDS in the Oral Solid Development department we are looking for an enthusiastic and dedicated colleague who shares our ambition to develop break-through synthetic molecules into oral solid dosage forms with a focus on Continuous Manufacturing and Dry Granulation (Roller Compaction).

We are currently seeking a Senior Scientist for Oral Solids Development at our Beerse site in Antwerp this pivotal role you will design and develop novel oral drug delivery systems scout and evaluate the external innovative solutions and support ongoing collaborations.

Key Responsibilities:

• Foster strong collaboration and networking within global teams.

• Enhance and ensure scientific expertise in synthetics development focusing on oral solid dosage forms and drug delivery systems more specifically on dry granulation formulation and process development.

• Drive innovation with a strong focus on customer needs and teamwork.

• Develop formulation strategies and processes that align with JJIMs commercial capabilities particularly concentrating on transforming small peptides into effective oral solid dosage forms.

Join our team and contribute to the development of innovative therapeutics that can significantly improve patient outcomes worldwide.

Your Impact:

As a key member of our PPDS development team you will significantly influence the future of drug formulation and process development. Your role will entail a wide array of responsibilities including:

• Contributing to the Formulation Development:Support and drive the formulation of synthetic molecules into oral solid dosage forms.

• Strengthening Stakeholder Relationships:Build and maintain robust relationships with cross-functional stakeholders collaborating with various departments such as Discovery Pharmaceutics Preclinical and Clinical Biopharmaceutical Sciences Analytical Development API Development Clinical Supply Chain Commercial Supply Manufacturing and Regulatory as well as with our Strategic External Partners such as CDMOs.

• Driving Innovation:Optimize existing processes and technology platforms using your expertise to develop novel therapeutic solutions. Identify and screen external innovations in process design tailored for Continuous Manufacturing of solid dosage forms.

• Collaborative Execution:Work closely with fellow scientists to design plan and carry out formulation development activities across our diverse product portfolio.

• Scientific Documentation:Diligently document scientific data and progress contributing to regulatory submissions scientific publications intellectual property initiatives and strategic decision-making.

• Regulatory Quality and Safety Compliance:Ensure adherence to regulatory standards Good Manufacturing Practices (GMP) and performance-based occupational exposure levels.

Join us in this exciting role to help shape the future of pharmaceutical innovations and enhance patient therapies!

What We Seek:

We are looking for a dynamic individual with a robust background in drug product formulation development specifically focused on oral small peptides. The ideal candidate will possess the following qualifications and attributes:

• Educational Background:A Ph.D. in Pharmaceutical Sciences Industrial Pharmacy Biochemical Engineering Chemical Engineering Biological or Physical Sciences or a related field with at least 3 years of relevant industry and/or academic experience. Alternatively a Bachelors or Masters Degree in relevant fields with a minimum of 10 years of relevant experience.

• Formulation Expertise:Demonstrated proficiency in formulation design and process development for synthetic molecules into oral solid dosage forms. Familiar with Continuous Manufacturing and Dry Granulation is a distinct advantage.

• Process Design and Development:Familiarity with application of predictive modelling tools and data sciences would be valuable assets for the position as well.

• Technological Implementation:Expertise in implementing advanced technologies related to drug formulation and development more specifically to dry granulation with the ability to determine critical quality attributes process parameters and material attributes.

• Willingness to Travel:A readiness to engage in international travel approximately 5-15% of the time.

If you are passionate about advancing the field of oral peptide development and possess the qualifications outlined we encourage you to join our team and make a meaningful impact in pharmaceutical innovation!

Required Skills:

Preferred Skills: