About this role
Purpose:
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, and final materials. Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner. Supports and leads operations & troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan. Stands in as Deputy for Manufacturing Supervisor in his/her absence. Major Responsibilities:
Plans and assigns daily production assignments to a team of Downstream biotechnologists.Operates with a high degree of technical expertise on the various purification processes: Chromatography, Filtration, Ultrafiltration, Final FillingDemonstrates initiative to problem-solve with various cross functions (e.g. Technical, Quality and Engineering)Coaches and trains junior biotechnologists in their area of workEnsures safe work environment in accordance with regulatory and global/local EHS policiesResponsible for the completeness and accuracy of all recordsEnsures that all batch related document errors are resolved in a timely manner to avoid batch review and release delaysCoordinates with various cross functions to provide windows for planned and unplanned downtimes.Drive performance to ensure execution is carried out flawlessly to ensure Human Error related events are preventedResponsible for overall plant upkeepDeputize in the absence of shift supervisor Bachelors in Sciences (i.e. Biologicals, Biomedical, Chemistry, Life Sciences, Pharmaceutical), Pharmacy, or Engineering (i.e. Biomedical, Chemical, Pharmaceutical), or equivalent Min 7 years of relevant work experience in Biologics / Pharmaceutical industry is required. Experience in leading a team is required Good interpersonal and communication skills required Excellent team player, with experience in shift work preferred Able to multi-tasks and work in a fast-paced environment preferred Can work under pressure, takes full ownership of tasks assigned and acts with personal integrity Strong problem solving and prioritization skills are required Knowledge of complex technical issues and manufacturing experience in a biopharmaceutical / pharmaceutical or similar environment
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.
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