Specialist, Scientific Compliance

Basic understanding of GxP drug development/medical device processes (working knowledge preferred).

Demonstrates customer-oriented behavior and works well in a fast-paced global team environment.

Familiarity with various software applications such as Microsoft platform (i.e., SharePoint, OneNote, Word, Excel, etc.), Smartsheet, Datavision, etc.

Basic understanding of R&D drug development/medical device processes (working knowledge preferred).

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

Ensure GxP compliance to AbbVie policies/processes/procedures, global regulatory requirements, and industry guidelines.

Remain current with major compliance trends and their application within the biopharmaceutical industry.

Serve as a business compliance liaison for Development Sciences (Dev Sci) scientific personnel involved in pipeline research and product development.

Collaborate with cross-functional teams, including personnel from Dev Sci, Legal Operations, Office of Ethics and Compliance, Corporate Affairs, Outsourcing, Pharmacovigilance & Patient Safety, Global Scientific Publications, external partners and vendors, and other R&D groups, to ensure compliance with relevant policies, regulations, and industry standards throughout all research and development activities.

Serve as a Business Publication Representative (BPR), streamlining and overseeing the centralized scientific publication approval process for Development Sciences.

Collaborate as part of a global BPR team, engaging with cross-functional stakeholders at all organizational levels to facilitate publication and compliance objectives.

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at

www.abbvie.com

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