Remote Senior Global Quality & Compliance Lead

Boehringer Ingelheim GmbH; Ridgefield (CT); Remote; USD 167,000 - 250,000; Full time

Benefits offered by this job

Discretionary bonus

Relocation assistance

Job summary

Boehringer Ingelheim is seeking a Senior Associate Director, Compliance Management (Remote) to lead GxP compliance strategy and improve quality processes globally. You will train teams, guide cross-functional projects, and drive CAPA effectiveness while partnering with regulatory bodies.

The role emphasizes risk assessments, regulatory inspections experience, and a high level of collaboration across Medicine and Quality functions. Travel as needed, with a competitive package.

Qualifications

• Bachelor’s or Master’s degree in a related field.
• Minimum 12 years in pharma/CRO industry.
• Minimum 7 years’ experience in Clinical Operations and/or BI Medicine functions.
• Minimum 5 years’ experience in NC/CAPA management, incl. Root Cause Analysis.
• 8+ years of experience in GxP quality management systems.
• Experience with regulatory authorities and inspections.
• Strong organizational and project management skills.
• Willingness to travel.

Responsibilities

• Define and deliver training for NC/CAPA and other compliance topics.
• Provide GxP guidance and share best practices across functions.
• Lead root cause analyses and implement CAPAs with effectiveness checks.
• Support IDE/Partnering projects with GCP compliance assessments.
• Contribute to clinical development strategy and risk-based improvements.

Skills

Interpersonal skills

Project management

GxP knowledge

Regulatory interactions

Communication skills

Risk assessment

Education

Bachelor’s degree

Master’s degree (MBA, MSc)

Job description

Boehringer Ingelheim is seeking a Senior Associate Director, Compliance Management (Remote) to lead GxP compliance strategy and improve quality processes globally. You will train teams, guide cross-functional projects, and drive CAPA effectiveness while partnering with regulatory bodies.

The role emphasizes risk assessments, regulatory inspections experience, and a high level of collaboration across Medicine and Quality functions. Travel as needed, with a competitive package.