Formulation Scientist

I am working with a leading CDMO offering end-to-end integrated solutions across the product lifecycle - from development and manufacturing to packaging and commercial launch. Our mission is to bring life-changing therapies to patients. We are currently expanding our formulation development capabilities in Spain and seeking a motivated Formulation Scientist to join our growing team.

Position Summary:

As a Formulation Scientist, you will be responsible for the design, development, and optimization of pharmaceutical formulations across a range of dosage forms. You will contribute to the successful development of drug products for clinical and commercial use, working in collaboration with cross-functional teams including analytical, manufacturing, and regulatory affairs.

Key Responsibilities:

• Design and develop formulations for oral solid dose, sterile injectables, or other dosage forms as per project requirements.
• Conduct pre-formulation studies and evaluate excipient compatibility.
• Prepare development batches and support scale-up activities in pilot and commercial manufacturing environments.
• Execute and interpret experimental protocols for formulation development, stability, and process optimization.
• Prepare technical reports, development summaries, and regulatory documentation (e.g., IMPDs, CTDs).
• Support technology transfer activities to internal or external manufacturing sites.
• Ensure compliance with GMP, regulatory guidelines, and company SOPs.
• Collaborate with cross-functional teams including analytical, clinical supply, QA, and regulatory affairs.
• Stay current with scientific and industry developments in pharmaceutical formulation.

Qualifications:

• MSc or PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related discipline.
• 2-5 years of experience in pharmaceutical formulation development (preferably CDMO environment).
• Hands-on experience with formulation equipment and technologies (e.g., granulation, lyophilization, tableting, coating).
• Strong understanding of physicochemical principles, excipient properties, and drug delivery systems.
• Experience with QbD, risk assessments, and DoE is a plus.
• Good knowledge of GMP and regulatory requirements (EMA, FDA).
• Strong organizational, problem-solving, and communication skills.
• Fluent in English; Spanish proficiency is a plus.

What We Offer:

• Opportunity to be part of a global, growing, and purpose-driven organization.
• Collaborative and innovative working environment.
• Career development and training opportunities.
• Competitive salary and benefits package.