Senior GMP Compliance & Process Excellence Specialist

Bristol Myers Squibb; Schweiz; Hybrid; CHF 90,000 - 130,000; Full time

Job summary

Bristol Myers Squibb is seeking a Senior Specialist Process Excellence Compliance to manage quality events and support inspection readiness in Switzerland. You will author GMP docs, drive CAPAs, and collaborate across functions to ensure regulatory compliance and continuous improvement.

The role requires a Life Sciences degree with 3–5 years in GMP compliance, strong communication, and ability to work under tight deadlines across multiple priorities. French and English proficiency is essential.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 3–5 years' experience in GMP compliance.
• Knowledge of regulatory requirements and audit processes.
• Experience with Health Authority inspections.
• Knowledge of pharmaceutical facilities, manufacturing, and laboratory systems, especially OSD.
• Strong communication and cross-functional collaboration.
• Ability to work under short deadlines with multiple priorities.
• Business level in French and English.

Responsibilities

• Own quality events and associated actions (CAPAs, Change Controls, complaints and deviations).
• Author and maintain GMP documentation and ensure timely approvals in the system.
• Contribute to inspection readiness and regulatory audits.
• Support root cause analysis.
• Contribute to quality KPI adherence.
• Perform impact assessments and risk evaluations.
• Drive local continuous improvement and site initiatives.
• Participate in compliance boards and forums.

Skills

GMP compliance

Regulatory knowledge

Audit readiness

Cross-functional collaboration

Documentation & SOPs

Verbal & written communication

Analytical problem solving

Time management

Education

Bachelor's degree in Life Sciences or related field

Job description

Bristol Myers Squibb is seeking a Senior Specialist Process Excellence Compliance to manage quality events and support inspection readiness in Switzerland. You will author GMP docs, drive CAPAs, and collaborate across functions to ensure regulatory compliance and continuous improvement.

The role requires a Life Sciences degree with 3–5 years in GMP compliance, strong communication, and ability to work under tight deadlines across multiple priorities. French and English proficiency is essential.