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

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

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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.

Contract: Freelance / Interim

Start: ASAP

Duration: at least 6 months

Where: Remote

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