R&D QC Project Lead

Lonza; Schweiz; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Inclusive workplace

Competitive compensation

Dynamic work culture

Zusammenfassung

Lonza in Basel, Switzerland is seeking an R&D Project Lead to drive pharmaceutical development projects from early phases to market readiness. You will ensure timely QC work-packages and documentation, and represent QC in internal and customer meetings.

You will proactively address risks, maintain cGMP/SOP compliance, support audits, and act as SME for QC topics while driving process improvements in a dynamic, inclusive workplace.

Qualifikationen

• MSc or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field.
• Experience in Analytics or Quality Control under cGMP regulations.
• Knowledge of analytical lifecycle for biotechnology products and CMC requirements.
• Strong communication and interpersonal skills with a proactive attitude.
• Detail-oriented and able to work in a matrix organization.
• Business fluent English, written and spoken.

Aufgaben

• Lead pharmaceutical development projects from early phases to market readiness
• Ensure timely delivery of QC work-packages and documentation
• Represent QC in internal and customer meetings
• Address risks proactively and communicate effectively
• Maintain compliance with cGMP and SOPs
• Support audits and act as SME for QC topics
• Drive process improvements and share best practices

Kenntnisse

Analytical chemistry knowledge

Quality control under cGMP

Project leadership

Communication skills

Matrix-organization experience

Ausbildung

MSc/PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field

Jobbeschreibung

Lonza in Basel, Switzerland is seeking an R&D Project Lead to drive pharmaceutical development projects from early phases to market readiness. You will ensure timely QC work-packages and documentation, and represent QC in internal and customer meetings.

You will proactively address risks, maintain cGMP/SOP compliance, support audits, and act as SME for QC topics while driving process improvements in a dynamic, inclusive workplace.