Oral Solid Dosage Formulation Scientist – Scale-Up & GMP

Try&Hire; Basel; On-site; CHF 90,000 - 120,000; Full time

Job summary

Try&Hire is seeking a scientifically minded professional to develop oral solid dosage formulations and lead manufacturing process development in Basel, Switzerland. The role covers from early-stage to GMP-compliant production, with onsite work and potential permanent placement after interim period.

You will plan experiments with cross-functional teams, document results, and transfer procedures to GMP facilities.

Qualifications

• Degree in Pharmaceutical Sciences or related discipline.
• 2–4 years of experience in pharmaceutical development.
• Experience with unit operations in lab/pilot plant.
• Experience using digital data recording tools.
• Strong knowledge of galenics and formulation/process development.
• Proficient with laboratory tools.
• English proficiency; German or French is a plus.

Responsibilities

• Plan, coordinate, perform and document scientific experiments with leads.
• Develop phase-appropriate formulations for oral drug products.
• Develop robust manufacturing processes including scale-up.
• Transfer procedures to GMP production facilities and troubleshoot.
• Support manufacture of clinical supplies under GMP conditions.
• Document and interpret raw data and propose next experiments.
• Contribute to investment projects and maintenance of infrastructure.

Skills

Pharmaceutical development

Oral solid dosage forms

Lab-scale-up expertise

e-Lab Notebook

GMP knowledge

English proficiency

German/French advantage

Education

MSc in Pharmaceutical Sciences

BSc with experience in pharma

Tools

e-Lab Notebook

Job description

Try&Hire is seeking a scientifically minded professional to develop oral solid dosage formulations and lead manufacturing process development in Basel, Switzerland. The role covers from early-stage to GMP-compliant production, with onsite work and potential permanent placement after interim period.

You will plan experiments with cross-functional teams, document results, and transfer procedures to GMP facilities.