(Senior) Formulation Scientist (complex injectables)

at  Delpharm Development NL

QUALIFICATIONS & SKILLS

• Hands-on attitude, passionate about lab work and process development.
• Master’s degree (MSc) in chemistry, pharmaceutical sciences, or a related field. A chemical background is essential.
• At least 5 years of hands-on experience in formulation and process development, particularly in injectables.
• Proven experience with small molecules proteins, peptides, microparticles, injectable gels, viscous liquids, and sterility.
• Demonstrated knowledge and application of Quality by Design (QbD).
• Preferably experienced with prefilled syringes and ophthalmic dosage forms.
• In-depth understanding of GMP, GLP, and process equipment selection.
• Strong problem-solving skills and the ability to work independently with minimal supervision.
• Excellent organizational skills, attention to detail, and the ability to manage multiple priorities effectively.
• Strong communication skills to collaborate cross-functionally and contribute to team success.

PURPOSE OF THE ROLE

As a (Senior) Formulation Scientist (complex injectables), you will play a key role in the development of scalable drug formulations while providing technical expertise and guidance to ensure project success. You will collaborate across teams in the lab and with the client to solve technical challenges, lead experiments, and contribute to regulatory submissions, ensuring alignment with Delpharm’s mission of delivering high-quality pharmaceutical solutions.

KEY RESPONSIBILITIES

• Lead the development of (complex) injectable formulations, with a focus on small molecules, proteins, peptides, microparticles, injectable gels, and viscous liquids.
• Apply expertise in process development and Quality by Design (QbD) to drive efficient and high-quality results.
• Design, plan, and execute scientific experiments aimed at developing scalable drug product formulations.
• Collaborate closely with Manufacturing and Tech Transfer teams to ensure seamless technology transfer and process scalability.
• Provide technical support to address challenges in formulation and process development, including prefilled syringes and ophthalmic applications.
• Assess material requirements and prepare for upcoming projects.
• Interpret data, provide recommendations, and document findings in digital notebooks, batch records, and scientific reports.
• Prepare and review documentation for regulatory submissions, including development reports and stability data.
• Write and review User Requirements Specifications (URS), Standard Operating Procedures (SOPs), and best practices.
• Guide and mentor (more junior) team members to foster a culture of growth and technical expertise.
• Contribute to equipment assessments and team development to align with operational and strategic goals.
• Support the team in writing quotations for prospective customers.