Analytical Development Project Lead – Small Molecules

Lonza; Schweiz; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career

Inclusive workplace

Competitive compensation

Lifestyle benefits

Zusammenfassung

Lonza in Visp, Switzerland, seeks a Project Manager for Analytical Development in Small Molecules to lead chromatographic method development and validation for API manufacturing. You will manage analytical activities, collaborate with Process Development, Manufacturing, QA, and QC, and guide a laboratory team.

Candidates should have a Ph.D. in Chemistry or Pharmacy or a related field, with strong chromatography skills, cGMP experience, and a customer-focused mindset.

Qualifikationen

• Ph.D. in Chemistry, Pharmacy, or related field, or Master’s with relevant experience.
• Strong knowledge of analytical methods with in-depth chromatography expertise.
• Experience in cGMP, API development, project management, and statistics is an advantage.
• Reliable, flexible, customer-focused, and quality-oriented mindset.

Aufgaben

• Act as the primary customer contact for analytical topics throughout project execution.
• Plan and execute analytical projects, ensuring regulatory requirements are met with cross-functional teams.
• Lead development, validation, and implementation of chromatographic analytical methods (HPLC, GC).
• Provide scientific and technical leadership within multifunctional project teams.
• Identify and implement emerging analytical technologies and innovative solutions.
• Lead and develop a laboratory team with a culture of collaboration and continuous improvement.

Kenntnisse

Chromatography

Analytical methods

Project management

HPLC

GC

Statistics

cGMP

Ausbildung

Ph.D. in Chemistry or Pharmacy (or related field)

Master's with relevant experience

Jobbeschreibung

Lonza in Visp, Switzerland, seeks a Project Manager for Analytical Development in Small Molecules to lead chromatographic method development and validation for API manufacturing. You will manage analytical activities, collaborate with Process Development, Manufacturing, QA, and QC, and guide a laboratory team.

Candidates should have a Ph.D. in Chemistry or Pharmacy or a related field, with strong chromatography skills, cGMP experience, and a customer-focused mindset.