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 authorizationsLead FDA and regulatory inspections effectivelyDevelop global and local Quality Management Systems as neededCollaborate with Medicine functions on quality objectivesConduct audits and handle findings decisivelyRequirements:Bachelor's degree required, advanced degree preferredMinimum 8 years of GCP experience in inspection managementStrong understanding of Quality by Design practicesProficiency in communication and leadership skillsExperience with project management techniquesLeverage your expertise in quality management and lead compliance initiatives at Boehringer Ingelheim.#J-18808-Ljbffr

📌 Quality & Compliance Senior Associate Director (Brampton)
🏢 Boehringer Ingelheim
📍 Brampton