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 www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Position Summary The QC Supervisor is responsible for leading and coordinating expert-level quality control activities supporting drug substance testing readiness and release, including method validation and QC analytical test approval, QC subcontracted testing oversight, stability report completion, and OOS/OOT investigation management. This role ensures all activities are executed in compliance with applicable cGMP requirements, internal procedures, data integrity standards, and agreed drug substance release timelines. Key Responsibilities + Supervise expert-level quality control activities. + Review, approve, and oversee method validation, drug substance and stability analytical test results in accordance with established procedures and quality standards. + Manage follow-up of subcontracted testing activities, including coordination with external laboratories, tracking deliverables, and ensuring timely closure of related actions. + Ensure timely completion, review, and approval of stability reports in line with study schedules, regulatory expectations, and program commitments. + Lead and coordinate OOS/OOT investigations, including root cause assessment, documentation, corrective and preventive actions, and cross-functional follow-up. + Monitor QC workflows to ensure alignment with DS release agreed timelines and proactively escalate risks to schedule or compliance. + Collaborate with QC operation teams, Manufacturing, QA, MS&T, Regulatory, and Supply Chain partners to support release readiness and issue resolution. + Ensure all testing, investigations, and documentation are completed accurately, thoroughly, and on time. + Contribute with the team to QC transversal continuous improvement initiatives focused on efficiency, compliance, and laboratory performance. + Coach and develop team members, promoting technical excellence, accountability, and compliance culture. + Lead and/or coordinate QC global SOP series updates and implementations in the department Qualifications + Bachelor’s degree in biology, chemistry, biotechnology or related scientific discipline. + Significant experience in QC laboratory operations within a pharmaceutical or biotech environment. + Strong knowledge of cGMP, analytical testing, stability programs, and OOS/OOT investigation processes. + Experience managing external laboratories or subcontracted analytical testing. + Fluency in English and French + Proven ability to prioritize and manage multiple deliverables against tight timelines. + Leadership, communication, documentation, prioritization and problem-solving skills. Additional Information 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