GMP Compliance & Process Excellence Specialist

Bristol Myers Squibb EU Policy; Boudry; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Zusammenfassung

Bristol Myers Squibb EU Policy is seeking a Senior Specialist Compliance Process Excellence to strengthen GMP documentation, risk assessments, and inspection readiness across manufacturing operations.

You will lead quality events, change controls, and continuous improvement initiatives, collaborating with cross-functional teams in a fast-paced pharmaceutical environment.

The role requires a life sciences degree, 3–5 years GMP experience, and fluency in French and English.

Qualifikationen

• Bachelor’s degree in Life Sciences or related field.
• 3-5 years in GMP compliance.
• Good collaboration and communication skills.
• 3-5 years of experience in pharmaceutical environment.
• Business Level in French and English.
• Experience in GMP inspections and audits.

Aufgaben

• Author and maintain GMP documentation, including SOPs, forms, and logbooks.
• Act as document owner, ensuring lifecycle management and compliance.
• Initiate and own quality events and deviation investigations.
• Perform and maintain risk assessments including manufacturing risk assessments.
• Support audit and inspection readiness and CAPA processes.
• Contribute to continuous improvement initiatives related to compliance.

Kenntnisse

GMP compliance

Collaboration

Communication

Bilingual French-English

GMP inspections and audits

Ausbildung

Bachelor’s degree in Life Sciences or related field

Jobbeschreibung

Bristol Myers Squibb EU Policy is seeking a Senior Specialist Compliance Process Excellence to strengthen GMP documentation, risk assessments, and inspection readiness across manufacturing operations.

You will lead quality events, change controls, and continuous improvement initiatives, collaborating with cross-functional teams in a fast-paced pharmaceutical environment.

The role requires a life sciences degree, 3–5 years GMP experience, and fluency in French and English.