Associate Specialist/Specialist

North Chicago, Illinois

AbbVie, Inc
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Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description RESPONSIBLITIES: Responsible for compliance with applicable Corporate and Divisional Policies and procedures. Ensure compliance with Quality System documents, including the creation and modification of procedures. Identify potential compliance risks and provide potential solutions, including implementation of solutions. Manage compliance and process improvement projects to enhance efficiency and compliance. Support internal and external audit activities, including providing pre-audit requests, acting as an SME during an audit and developing and completing audit commitments. Work cross-functionally in a team environment to develop/shape quality system and corporate policy. Anticipate and respond to unexpected occurrences and business needs. Adhere to codes of conduct and ethical principles. Provide guidance on regulatory and compliance requirements/expectations. Ability to work independently to identify and solve issues as they arise. Ability to use good judgment when implementing solutions independently and to discern which issues should be raised to management. Ability to manage several tasks simultaneously. Able to adjust rapidly to significant changes in direction and environment with minimal impact on productivity. Significant Work Activities -Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Qualifications QUALIFICATIONS: BS in a scientific discipline or equivalent experience. Experience working within GLP, GMP and GCP regulations preferred. Experience working in a R&D environment preferred. Ability to facilitate meetings and work well in a project team environment. Good oral, written, interpersonal and presentation skills. Working knowledge of drug development process preferred. We can hire at either level depending on experience level. Additional Information Applicable only to applicants
Date Posted: 21 March 2024
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