IT Compliance Lead GMP & CSV (Pharma)

Biopharma Careers; Boudry; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Bristol Myers Squibb is seeking an IT Compliance Manager II to lead quality oversight of GPS IT Boudry systems. Based in Boudry, Switzerland, you will drive risk-based activities, collaborate across functions, and ensure continuous compliance with GMP and regulatory standards.

The role requires 5–7 years in pharma IT compliance, CSV expertise, and strong English (French a plus). You will mentor teams, manage system lifecycle, and support audits at the Boudry site.

Qualifikationen

• Experience with pharmaceutical IT compliance and quality systems.
• Strong knowledge of GxP requirements and validation.
• Familiarity with regulatory frameworks (21-CFR Part 11, EudraLex, MHRA).

Aufgaben

• Interpret, implement, and monitor IT quality systems to ensure GMP compliance.
• Serve as main liaison between GPS IT Boudry and QA Compliance.
• Lead cross-functional IT compliance initiatives and participate in audits.

Kenntnisse

GxP systems knowledge

CSV (Computer System Validation)

IT infrastructure & networks

Quality Management Systems

Regulatory knowledge (21-CFR Part 11,E

Ausbildung

Bachelor's/Master's in Quality, Engineering, Sciences

Tools

CSV

Jobbeschreibung

Bristol Myers Squibb is seeking an IT Compliance Manager II to lead quality oversight of GPS IT Boudry systems. Based in Boudry, Switzerland, you will drive risk-based activities, collaborate across functions, and ensure continuous compliance with GMP and regulatory standards.

The role requires 5–7 years in pharma IT compliance, CSV expertise, and strong English (French a plus). You will mentor teams, manage system lifecycle, and support audits at the Boudry site.