Direct message the job poster from AL SolutionsExpert in linking Commercial & C-Suite Professionals to Biotech and CDMOs throughout the United States & Europe.
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.Seniority level
Seniority level AssociateEmployment type
Employment type Full-timeJob function
Job function ResearchIndustries Pharmaceutical Manufacturing and ManufacturingReferrals increase your chances of interviewing at AL Solutions by 2xWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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