QC Data Reviewer I (2pm-10:30pm)

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 . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok .

Job Description

Purpose

The QC Data Reviewer I review data from laboratory testing within a fast paced GMP environment to support one or more of the following areas: raw materials, in-process product, final bulk, stability, environmental monitoring, microbiology and or validation. Reviews data for compliance to SOP, protocol and GMP requirements. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in review of data to support investigations.

Responsibilities

• Reviews data from laboratory testing to support product/material release
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements
• Understand, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements
• Accepts responsibility to complete assigned tasks as committed. Works with other to maintain a positive atmosphere to accomplish business objectives
• Able to interpret and perform data review on results from complex lab tests with minimal error. ·
• Able to guide lab analysts on mitigation of documentation errors (Op note, aberrant peak forms...) ·
• Participatory in continuous improvement projects, and change request (CR Processes/Processing)
• Basic leadership of small projects and change management (i.e. annual logbook reconciliation/issuance, · archive process maintenance…)
• Review of raw data for non-routine studies where protocols are already written and approved.

Qualifications

Qualifications

• BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.
• 2+ years of related work experience
• Maintains their certifications as needed for assigned job tasks.

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. ​

• This job is eligible to participate in our long-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.

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