Associate Specialist, Quality Systems

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, Facebook, Instagram, X and YouTube.

The Associate Specialist Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, combination products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.

Responsibilities:

• Assist with proper integration and support of quality regulations: drug, biologics, device and/or combination products.
• Conduct initial regulatory review of documents.
• Assist with audits of documentation, facilities and equipment.
• Complete and route change requests for process document creation, maintenance, and implementation.
• Support project teams in planning, preparation, review and approval of quality documentation.
• Collect and compile key quality metric data.
• Perform QA review for product release.
• Participate in training and education programs for various aspects of quality assurance.

Qualifications:

• Bachelor’s Degree (Chemistry, Pharmacy, Biology, Microbiology, Engineering or other Technical/ Scientific, area preferred) or equivalent experience.
• Two (2) years’ experience in quality assurance, quality oversight or relevant experience.
• Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological and medical device products, preferred.
• Strong oral and written communication skills needed.
• Excellent interpersonal skills a plus.
• Delivers tactical results to support the quality system.

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 atthe time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors includinggeographic 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 aparticular 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