Global TRD Quality Project Lead - Contract

Novartis; Basel; Vor Ort; CHF 150.000 - 180.000; Vollzeit

Zusammenfassung

Novartis, via Magnit Global, seeks a contractor to lead TRD QA teams and ensure quality across complex projects. You will guide QA activities, oversee regulatory readiness, and support submissions, reporting to global QA leadership.

This 12-month onsite role begins 1 January 2027 in Basel and requires strong pharmaceutical quality expertise. The position emphasizes cross-functional collaboration, risk management, and inspection readiness in drug/product development environments.

Qualifikationen

• Minimum: Bachelor’s degree with >10 years pharma quality/operations.
• Desirable: Master’s degree with >5 years pharma quality/operations.
• Fluent English required (oral & written).
• Broad knowledge of quality standards in Drug Product/Medical Devices manufacturing.

Aufgaben

• Lead global TRD QA teams and represent QA at global project board meetings.
• Oversee quality guidance across development projects and ensure compliance with cGMP.
• Contribute to project strategy, risk assessments, and contingency planning.
• Support PAI preparation, Mock-PAI, and submission readiness.
• Coordinate QA contracts and amendments with third parties.
• Lead cross-functional initiatives and ensure timely quality deliverables.

Kenntnisse

Quality Assurance

Project management

cGMP knowledge

Regulatory inspections

Cross-functional work

English fluency

Documentation systems

MS Office

Ausbildung

Bachelor's degree

Master's degree

Tools

MS Office

Document management systems

Jobbeschreibung

Novartis, via Magnit Global, seeks a contractor to lead TRD QA teams and ensure quality across complex projects. You will guide QA activities, oversee regulatory readiness, and support submissions, reporting to global QA leadership.

This 12-month onsite role begins 1 January 2027 in Basel and requires strong pharmaceutical quality expertise. The position emphasizes cross-functional collaboration, risk management, and inspection readiness in drug/product development environments.