Quality Assurance Manager

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 through our Allergan Aesthetics portfolio. Job Overview The Quality Assurance Manager provides quality assurance support for manufacturing processes of pharmaceutical products, medical devices, cosmetics, combination products, and biologics. The role ensures 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. The Manager translates strategy into tactical objectives, delivers strategic plans and regulatory updates, and leads a team of QA professionals. Key Responsibilities Provides direction to staff of professionals to include hiring, setting performance expectations, performance feedback, and development of staff Directs the development of Quality policies that meet both regulatory and company requirements. Maintains expertise on various regulations (FDA, EMA, ICH, etc.) Provides compliance leadership to the manufacturing site. Provides direct interface with FDA and other regulatory agencies and customers during inspections. Performs assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within our quality system. Reviews and approves deviation investigations, driving reduction in quality events through robust CAPA Compiles, analyzes and communicates significant quality or compliance metrics to senior management Establishes programs to promote quality awareness and compliance Qualifications Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred. 8+ years’ experience in quality assurance, quality oversight or relevant experience. Leadership of technical professionals and in leading cross‑functional teams. Technical knowledge in as many of the following areas as possible: Quality, Regulatory, Process Sciences, Manufacturing Operations. Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products. Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products. Experience working in both team setting and independently. Works well with manager guidance while able to manage own time. Strong oral (with all levels of management) and written communication skills needed. Excellent interpersonal skills a plus. Can lead medium to larger sized projects with increasing level of complexity and size to deliver tactical results that support strategic initiatives. Additional Information 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 long‑term incentive programs. Equal Opportunity Employer 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. Reasonable Accommodation US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: #J-18808-Ljbffr