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.
