Specialist, Scientific Compliance II

AbbVieVerified source: this listing comes from the employer's official hiring system or a verified company · North Chicago, United States · Onsite
Listed via SmartRecruiters
Posted Jun 1, 2026 · Apply by Sep 15
Recently checked

Last checked active on Jul 26, 2026.

Position Overview

Compensation: Not disclosed
Position: Mid
Type: Job
Employment: Full time
Practice Area: Compliance
Remote: No
Deadline: Sep 15, 2026

Job Description

Company Description

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. Follow @abbvie on LinkedIn, FacebookInstagramX and YouTube.

Job Description

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. Proactively evaluate organizational compliance needs and evaluate opportunities to improve efficiency and productivity.

Responsibilities

  • Adhere to codes of conduct and ethical principles and ensure compliance with applicable AbbVie policies and procedures.
  • Utilize systems, documents, and tools to provide compliance support for centralized business function processes
  • Manage compliance and process improvement initiatives to enhance efficiency and compliance.
  • Anticipate and respond to unexpected occurrences and business needs.
  • Identify and appropriately escalate potential compliance risks, and recommend practical solutions and implementation plans.
  • Work in a highly team-based, cross-functional team environment for daily activities/decision-making, and provide input to develop/shape quality system and corporate policy.
  • With limited oversight, manage several tasks simultaneously and adjust rapidly to significant changes in direction and environment with minimal impact on productivity.
  • Provide input to regulatory and compliance requirements/expectations
  • May supervise contract personnel.

Qualifications

  • Minimum of Bachelor's degree (scientific field preferred)
  • Typically 7 (Bachelor's), or 5 (Master's) years related industry (i.e. GxP) experience.
  • Experience working in a R&D environment preferred.
  • Working knowledge of GxP drug development/medical device processes.
  • Good interpersonal skills with ability to effectively communicate in a clear and persuasive manner; proficient in business/technical communications
  • Good organizational and time management skills, strong attention to detail.
  • Demonstrates customer-oriented behavior and works well in a fast-paced global team environment.
  • Experience working with a variety of disciplines and global teams in fast-paced environments.
  • Exhibits problem-solving and analytical skills.

Additional Information

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. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Perks & Benefits

Health Insurance, 401(k) Plan, Paid Time Off

Practice Area

Position

Mid

Required Skills

Analytical Skills, Attention to Detail

Industry

Legal

Application Deadline

September 15, 2026

Employment Type

Full time

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