Specialist II, US Product CMC Regulatory Affairs (Hybrid)
Boehringer Ingelheim International•Ridgefield, CT
399d•Hybrid
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About The Position
The Specialist II, US Product CMC Regulatory Affairs role at Boehringer Ingelheim involves providing operational and logistical support for regulatory submissions and compliance tasks related to Chemistry, Manufacturing, and Controls (CMC) for standard drug products. This hybrid position requires working on-site in Ridgefield, CT, 2-3 days a week, and offers opportunities for collaboration and contribution to the company's success in the pharmaceutical industry.
