SThree Deutschlandweit vor 1 Wochen

Interim Pharmaceutical Crystallization & Solid-State Consultant (f/m/d)

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Contract: Freelance / Interim Start: ASAP Duration: at least 6 months Where: Remote

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Interim Pharmaceutical Crystallization & Solid-State Consultant (f/m/d) We are currently seeking an experienced Senior Pharmaceutical Crystallization & Solid-State Consultant to support a leading pharmaceutical organization in the review, optimization, and scale-up of small molecule crystallization and solid-state development activities.

Key Responsibilities: • Review and assess crystallization and co-crystal development activities performed by external development partners and CDMOs. • Provide expert guidance on the development, optimization, and scale-up of robust pharmaceutical crystallization processes. • Support troubleshooting activities related to crystal form selection, morphology, yield, and downstream processability. • Advise on crystallization strategies, experimental design, process parameters, and analytical approaches. • Assess scalability from laboratory to pilot and commercial manufacturing scale, identifying critical technical risks. • Evaluate the impact of solid-state and particle properties on API processing and drug product performance. • Provide independent technical recommendations and support strategic development decisions.

Required Expertise: • MSc or PhD in Chemistry, Physical Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline. • Extensive industry experience in small molecule pharmaceutical crystallization, solid-state development, and/or particle engineering. • Proven track record in the successful development and scale-up of crystallization processes. • Strong expertise in pharmaceutical solid-state and particle characterization techniques. • Experience with pharmaceutical co-crystals is highly desirable. • Understanding of the relationship between API solid-state properties, downstream processing, and formulation performance. • Previous experience working with or managing external CDMOs is an advantage. • Knowledge of formulation development for poorly soluble small molecules is a plus.

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