Company Description

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 products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Purpose Statement

Performs functions associated with cGMP manufacturing operations within the biologics production facility.Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.Serves as a highly skilled subject matter expert within the manufacturing area, contributing to the development of concepts, techniques, and process improvements.Supports and drives troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan. 

Major Responsibilities:

To perform purification operations that include column chromatography, tangential flow filtration, Viral filtration and Bulk filling in Glovebox within the biologics production facilityExecute on computerized systems (such as Delta V, SAP and MES) for process control and data entryAdhere to safety requirements in all tasks, report incidents and near misses promptly, and assist with Safety, Health, and Environmental (SHE) incident investigations.Participates in resolution of anomalous processing eventsAssists lead in planning production schedule and leading area activitiesPerforms advance process and equipment troubleshootingCoach and train junior biotechnologists in area of expertiseSets a positive team environment and inculcates a nurturing AbbVie culture
Qualifications
Bachelor Degree education with at least 5 years of experience working in Biologics Production facility or equivalentMinimally 3+ years prior experience in large scale GMP purification manufacturingCompletes complex tasks in creative and effective waysConsistently works on complex assignments requiring independent action and a high degree of initiative to resolve issuesComfortable working in clean room environmentsActs independently to determine methods and procedures on new assignments with high learning agilityShift work is required
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