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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