Quality Systems Analytics Specialist, (Onsite)

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. 

We are looking for a skilled Quality Systems Analytics Specialist to join our team at the Branchburg site. This position offers a unique opportunity to lead and develop a data-driven culture within our quality organization and site, reporting directly to the Executive Director of quality.

As the Quality System Analytics Specialist, you will be responsible for analyzing and resolving problems, providing insights, and identifying areas for improvement. Your expertise in quality systems and data will play a crucial role in driving the success of our site. Additionally, you will contribute to resource planning and policy development.

In this role, you will be vital in authoring, co-authoring, reviewing, and approving data reports and presentations for various stakeholders, including quality managers, senior management, internal technical groups, and regulatory agencies. Your recommendations for corrective actions will ensure compliance and continuous improvement. You will also be responsible for developing efficient data reporting systems that transform raw data into actionable information.

The impact of this position is significant, as your work will ensure overall compliance with regulations for metrics reporting and drive a metrics system that promotes ethical decision-making. Your contribution will also ensure the delivery of safe and compliant products to our customers and patients. Furthermore, you will be pivotal in fostering a culture of accountability and data-driven decision-making within the quality organization and at our Branchburg site.

Suppose you are passionate about quality systems, possess strong data expertise, and thrive in a dynamic environment. In that case, we invite you to apply for this position and be part of our team, which is dedicated to delivering excellence in quality and compliance.

Responsibilities:

• Manage critical metrics for the Branchburg Quality organization, including Quality Index, Site Business Review, Quality Systems Management Review, and Post Market Surveillance Review.
• Provide in-depth insights for each metric, understand the context and drivers for any misses, and represent Branchburg in above-site reviews when required. Own and maintain procedures for Post Market Surveillance, Quality Management System Review, and other assigned procedures.
• Understand the various systems that house quality data and records and extract data as needed, depending on the information required.
• Lead the establishment of a metrics-driven culture across the organization, collaborating with key stakeholders to understand data sources, limitations, and opportunities for leveraging data.
• Develop standard work, enhance knowledge and skills, and integrate metrics into tier structures to drive actions and share best practices.
• Generate ad hoc reports, develop analytics tools, and use visualization/BI tools to create automated dashboards.
• Collaborate cross-functionally to drive corrective actions to improve metrics. Ensure key metrics are integrated into Tier and monthly review processes.
• Collaborate cross-functionally on complaint trend monitoring, evaluation, and investigation of signals and potential trends. Generate and maintain Post-Market Surveillance Plans and Periodic Safety Update Reports according to required timelines for medical devices.
• Monitor and implement processes to ensure compliance with regulations and guidelines, including FDA 21CFR 1271 and 820, ISO 9001 and 13485, EU MDR, Health Canada regulations, AATB, and state regulations.

Onsite position in our Branchburg, NJ location.

• Bachelor's degree in Science, Business, Engineering, or related discipline, or equivalent work experience with 3 to 5 years of experience in Medical Device, Pharmaceutical, Human Tissue, or other regulated industries is required.
• 3-5 years of experience in quality analysis, operations analysis, or other quality-related responsibilities.
• Demonstrated knowledge in Quality Systems, Regulations, and Standards.
• Data-driven with strong problem-solving skills and a focus on continuous improvement.
• Excellent communication skills at all levels (written and verbal) and attention to detail.
• Demonstrated proficiency with Minitab, Power BI, and Microsoft Office Suite, especially PowerPoint, and advanced Excel skills  (Power Query, pivot tables, complex formulas, etc.) requiere.
• Familiarity with business systems such as SAP and Global TrackWise is preferred.
• Lean, Six Sigma training, and expertise are preferred.

#LI-Onsite

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, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html