Associate Quality Systems Analyst

About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

This position is responsible for the following:

• Assisting with the compilation and analysis of data required to support Annual product reviews, which includes, but is not limited to revisions to Product Specifications, Manufacturing and QC Master Records; Final Release Inspection results; Stability results; and Product Complaint information.
• Aiding with the preparation of annual product review reports according to product schedule.
• Assisting with performing Internal audits in adherence with the annual Internal audit schedule.
• Assisting with Duties in Quality Documentation Group - including but not limited to maintaining and facilitating the review and approval of controlled documents such as SOP's, Master Records, project documents etc. maintenance of controlled document storage, issuance, retrieval and maintenance of logbooks.
• Performing other duties as assigned.

Qualifications

Education, Skills & Abilities:

• Bachelor's Degree in a science or related field preferred, or equivalent combination of education and experience required.
• Minimum two (2) years of experience in a laboratory or quality role.
• Advanced Microsoft Office, Proficient in Microsoft Word and Excel.
• Experience in a regulated environment preferred.
• Experience in the manufacture of pharmaceuticals.
• Excellent analytical and problem-solving skills; ability to analyze data.
• Excellent oral and written communication skills.
• Excellent proofreading skills.
• Technical writing skills and trouble shooting skills preferred.
• Ability to work effectively with peers and supervisors.
• Working knowledge of cGMP's and QA systems.

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.