Associate Specialist, Scientific Compliance

📋 Description

• Ensure GxP compliance to AbbVie policies/processes/procedures, global regulatory requirements, and
• Remain current with major compliance trends and their application within the biopharmaceutical
• Serve as a business compliance liaison for Development Sciences (Dev Sci) scientific personnel
• Collaborate with cross-functional teams, including personnel from Dev Sci, other R&D groups
• Ensure compliance with Quality System (QS) documents, including the creation, modification, and
• Collaborate as part of a global document management team, engaging with cross-functional

🎯 Requirements

• Minimum of Associate's degree (scientific field preferred).
• Typically 3 (Associate's), or 0-2 (Bachelor's) years of industry related (i.e. GxP) experience.
• Experience with document management processing is preferred.
• Familiarity with various software applications such as Microsoft platform (i.e., SharePoint
• Basic understanding of R&D drug development/medical device processes preferred.
• Good interpersonal skills with ability to effectively communicate in a clear manner; proficient in

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance and 401(k) to eligible employees
• Eligible to participate in short-term incentive programs