GMP Compliance & Process Excellence — Commercial Ops

Bristol Myers Squibb; Boudry; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Bristol Myers Squibb in Neuchâtel, Switzerland is seeking a Senior Specialist Compliance Process Excellence in Commercial Operations. The role focuses on GMP documentation, risk assessments and quality processes to support manufacturing readiness and regulatory compliance.

The successful candidate will bring 3–5 years in GMP and pharmaceutical environments, plus strong collaboration and French/English language skills, to drive continuous improvement and effective audits.

Qualifikationen

• Bachelor’s degree in Life Sciences or related field.
• 3–5 years in GMP compliance.
• 3–5 years of experience in pharmaceutical environment.
• Business level in French and English.
• Experience in GMP inspections and audits.

Aufgaben

• Author and maintain manufacturing GMP documentation, including SOPs, forms, and logbooks
• Act as document owner, ensuring lifecycle management and compliance
• Initiate and own activities from initiation to closure for CAPA, Change Controls, and deviations
• Participate to deviation investigation when needed
• Initiate Supplier Corrective Action Requests (SCARs)
• Participate to Communities of Practice (CoPs)
• Own, perform, and maintain risk assessments, including Manufacturing Risk Assessments
• DIRA and associated summary reports
• Act as Manufacturing SPoC for inspection readiness
• Continue to responses coming from audit observations and inspection findings
• Support local continuous improvement initiatives related to compliance, process effectiveness, and inspection readiness

Kenntnisse

GMP compliance

Pharma experience

Collaboration

Communication

French language

English language

Audits & inspections

Ausbildung

Bachelor’s degree in Life Sciences or related field

Jobbeschreibung

Bristol Myers Squibb in Neuchâtel, Switzerland is seeking a Senior Specialist Compliance Process Excellence in Commercial Operations. The role focuses on GMP documentation, risk assessments and quality processes to support manufacturing readiness and regulatory compliance.

The successful candidate will bring 3–5 years in GMP and pharmaceutical environments, plus strong collaboration and French/English language skills, to drive continuous improvement and effective audits.