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.

Purpose

Serves as the lead for the evaluation, implementation, and continuous improvement of laboratory technologies, workflows, and systems supporting New Product Introductions (NPIs), existing product enhancements, and lab transformation initiatives. Serves as the key liaison between QC laboratories, IT, and global functional stakeholders to drive high-impact projects. Provides subject matter expert guidance on test method validation and transfer, lab efficiency, safety, and compliance strategies while mentoring peers and championing innovation across laboratory operations.

Responsibilities

• Leads planning and execution of New Product Introductions (NPIs) within the QC laboratories including evaluation of test methods, instrumentation, lab readiness, and training strategies. Primary point of contact for new testing requests on existing products.
• Serves as the primary QC laboratory representative for cross-functional initiatives, representing QC perspectives in global teams and and working with sites in the global network to ensure new test methods and/or technologies are being implemented and executed consistently across the enterprise.
• Works with the Environmental Health and Safety group and appropriate colleagues to develop and implement safety evaluations and proactive risk mitigation control strategies in alignment with regulatory and organizational standards.
• Drives continuous improvement initiatives, leveraging data-driven analysis to enhance laboratory workflows, efficiency, and system/method implementation.
• Serves as the QC subject matter expert and laboratory representative on cross-functional project teams, providing strategic direction, task delegation, and coaching to laboratory team members to ensure timely and successful project delivery.
• Arranges NPI and project support training, ensuring knowledge transfer and laboratory readiness for new and updated testing platforms.
• Conducts financial evaluations of lab initiatives, including resource planning, cost efficiency recommendations, and ROI assessments. Oversees material and equipment procurement planning, working with the procurement and finance department to ensure alignment with project timelines and budgets.
• Drives method remediation and equivalency studies ensuring scientific integrity and alignment for legacy and evolving methods.
• Manages system configuration and deployment of chromatography and laboratory information management systems to support evolving lab needs, including the development and validation of custom calculations.
• Serves as a subject matter expert in method co-validation and transfer, providing consultation to global partners and mentoring less-experienced colleagues.

• Bachelor’s Degree in Science, Engineering or applicable discipline.
• 7+ years’ experience in a regulated or pharmaceutical Quality laboratory environment.
• Skilled in creating and executing validation and transfer protocols, method development/remediation, and managing controlled documentation.
• Ability to lead complex, multi-site or global initiatives involving diverse stakeholder groups.
• Experience in equipment procurement and project financial evaluation.
• Knowledge of laboratory informatics platforms (e.g., Empower, SampleManager, etc.)
• Strong analytical, organizational, and communication skills.
• Travel required up to 5% of the time

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 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 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 a particular 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