Associate Director, Quality Control (bulk & intermediate biopharmaceuticals manufacturing, immunology, oncology, & other therapeutic use) 3 days ago Be among the first 25 applicants Company Description

While professional experience and qualifications are key for this role, make sure to check you have the preferable soft skills before applying if required. 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 www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Key Responsibilities Manage QC laboratory including setting of vision & strategy, develop & manage operating budgets, management of large group of technical employees, project management, & unit operational management to support overall business operations. Provide technical leadership in a multidisciplinary environment to ensure activities are on track per business needs & established timeline. Serve as an expert in technical/functional areas. Create & review quality system documents including test procedures, validation & technical protocols & reports, lab investigations, manufacturing records & quality control data. Establish & execute plans & commitments consistent with Development, Manufacturing, Customers & Business needs. QualificationsEducation & Experience Must have a Bachelor’s Degree preferably in Physical or Life Sciences, Pharmacy, or Engineering & 5 years of management experience in QC. At least 5 years of experience managing a team of at least 10 QC analysts, performing biopharmaceutical testing within the biologics industry, using Quality policies, cGMP & other regulatory requirements, and managing QC clinical & commercial projects across multifunctional teams including manufacturing, materials management, engineering, product development, Quality Systems, Product QA, Quality Control, Information Systems & Regulatory Affairs. Additionally, at least 3 years of experience using statistical quality systems, electronic document management & laboratory information management. Work experience may be gained concurrently. Additional Information Salary Range: $201,587.12 - $261,000.00 per year. Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF41403T. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k). This job is eligible for participation in our short-term and long-term incentive programs. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. We are an equal opportunity employer and do not discriminate based on race, color, religion, national origin, age, sex, disability, or other protected status.

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