NOVADIP Biosciences S.A.

About the Company

Novadip Biosciences is a clinical-stage biopharmaceutical company founded to design, develop, and bring to the market a new class of regenerative tissue products to accelerate healing of large bone defects and injuries in a single treatment. Novadip’s lead allogeneic product, NVD-X3, employs a matrix containing multiple bioactive factors that induce accelerated tissue healing. Designed as an “off-the-shelf” product, NVD-X3 can be shipped and stored at room temperature and offers superior intraoperative handling characteristics. Novadip is also developing NVD-003, an autologous therapy derived from ASCs as a potential single treatment to save limbs and restore mobility in patients with congenital pseudarthrosis of the tibia (CPT). CPT is a rare pediatric bone condition. Learn more about our technology platform and clinical development programs at www.novadip.com Phone number: +32/10 77 92 20 E-mail: info@novadip.com VAT: BE0535.575.602 Privacy policy: https://novadip.com/privacy-policy/

Listed Jobs

Company Name

NOVADIP Biosciences S.A.

Job Title

Process Development Scientist

Job Description

Job Title: Process Development Scientist Role Summary: Lead the design, optimization, and industrialization of pharmaceutical production processes, performing GMP activities, validation, and technology transfer while collaborating with Clinical Manufacturing, QC, and QA teams. Expectations: Deliver robust, scalable processes; ensure compliance with GLP, GMP, GDP; maintain accurate documentation; support cross‑functional initiatives. Key Responsibilities - Identify and implement process improvements to enhance yield, quality, and cost efficiency. - Design, develop, and validate manufacturing processes and equipment, following protocols and guidelines. - Schedule, supervise, and complete development and validation activities within defined timelines. - Plan material requirements and coordinate resources for timely execution of projects. - Produce regular progress reports for project stakeholders. - Ensure strict adherence to GLP, GMP, GDP standards and maintain traceability of manufacturing data. - Draft and maintain protocols, reports, and other documentation for development and validation studies. - Execute technology transfer in collaboration with operational departments when required. - Collaborate with QA to develop and update SOPs, protocols, and reports. - Investigate and document non‑conformities or deviations, initiating corrective actions. - Provide operational support to Manufacturing and QC teams as needed. Required Skills - Cell culture techniques and aseptic handling; at least 2 years of practical experience. - Strong understanding of GMP requirements and GMP documentation practices. - Process design, validation, and industrialization expertise. - Ability to manage multiple tasks, prioritize, and meet deadlines. - Meticulous record‑keeping, strong organizational skills, and attention to detail. - Excellent interpersonal and teamwork abilities; effective communication across departments. Required Education & Certifications - Bachelor’s or Master’s degree in Biological Sciences, Life Sciences, or related field. - Formal training or certification in GMP, GLP, or related regulatory standards is desirable.

Mont-saint-guibert, Belgium

On site

Junior

08-12-2025