Job Summary: The Principal Regulatory Affairs Specialist is expected to perform with minimal supervision and is responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory approval, preparing global submissions, and ensuring timely and high-quality execution of all regulatory deliverables. In addition, the Principal Specialist mentors other regulatory specialists, and provides support for global regulatory approvals (beyond US and EU), commercialized products, and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements. This position includes supporting internal and external customer regulatory requests. This position can accommodate a remote work locatio
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