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.
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 facility
- Execute on computerized systems (such as Delta V, SAP and MES) for process control and data entry
- Adhere 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 events
- Assists lead in planning production schedule and leading area activities
- Performs advance process and equipment troubleshooting
- Coach and train junior biotechnologists in area of expertise
- Sets a positive team environment and inculcates a nurturing AbbVie culture
- Bachelor Degree education with at least 5 years of experience working in Biologics Production facility or equivalent
- Minimally 3+ years prior experience in large scale GMP purification manufacturing
- Completes complex tasks in creative and effective ways
- Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues
- Comfortable working in clean room environments
- Acts independently to determine methods and procedures on new assignments with high learning agility
- Shift work is required
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