Parenteral Formulation & Process Development Scientist

Roche; Basel; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Zusammenfassung

Roche in Basel, Switzerland seeks a Scientist in Pharmaceutical Development to drive end-to-end parenteral formulation development, from liquid to lyophilized forms, and to establish scalable manufacturing processes for clinical and commercial transfer.

You will lead cross-functional teams, contribute to regulatory submissions (BLA/MAA/NDA), and collaborate with Postdocs and Scientists to test new modalities, including oligonucleotides, within a dynamic and collaborative environment.

Qualifikationen

• Ph.D. or master's in chemistry, chemical/process engineering or related fields.
• Minimum of 2 years of professional experience in formulation and process development for parenteral dosage forms.
• Experience in oligonucleotides is a plus.

Aufgaben

• Lead the end-to-end development of parenteral formulations—including liquid and lyophilized dosage forms—and establish robust manufacturing processes from scale-up and characterization to commercial transfer.
• Represent Pharmaceutical Development as a project leader in global CMC and cross-functional teams, providing critical technical expertise and strategic input for regulatory submissions (BLA/MAA/NDA) throughout all clinical stages.
• Actively apply creative, open-minded approaches to overcome unfavorable molecular properties. Serve as a key lab partner to Postdocs and Scientists to test and validate exploratory formulation concepts and new therapeutic modalities.
• Manage and support analytical method scouting, analytical understanding and implementation capabilities in our routine.

Ausbildung

Ph.D. or master degree in chemistry, chemical/process engineering or related fields

Jobbeschreibung

Roche in Basel, Switzerland seeks a Scientist in Pharmaceutical Development to drive end-to-end parenteral formulation development, from liquid to lyophilized forms, and to establish scalable manufacturing processes for clinical and commercial transfer.

You will lead cross-functional teams, contribute to regulatory submissions (BLA/MAA/NDA), and collaborate with Postdocs and Scientists to test new modalities, including oligonucleotides, within a dynamic and collaborative environment.