Drive quality and compliance at Boehringer Ingelheim as a Senior Associate Director in Ridgefield, CT. This hybrid role combines regulatory insight and quality management expertise to ensure optimal product development.
In this senior role, you will provide crucial consultancy for quality and compliance within the U.S., channeling insights from local practices into the global strategy. With the flexibility of hybrid work, you will lead inspections and collaborate with various business functions to ensure regulatory adherence and optimally implement quality standards from the start.
Key Responsibilities:
• Provide compliance consultancy during research and market authorizations
• Lead FDA and regulatory inspections effectively
• Develop global and local Quality Management Systems as needed
• Collaborate with Medicine functions on quality objectives
• Conduct audits and handle findings decisively
Requirements:
• Bachelor’s degree required, advanced degree preferred
• Minimum 8 years of GCP experience in inspection management
• Robust understanding of Quality by Design practices
• Proficiency in communication and leadership skills
• Experience with project management techniques
Leverage your expertise in quality management and lead compliance initiatives at Boehringer Ingelheim.
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