Join our Talent Pipeline for Manufacturing Supervisor - #1120904
Abbvie
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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
Join our Talent Pipeline!
Thank you for considering a future opportunity with our company! We are currently not actively hiring for this specific role and would love to connect with talented individuals who are interested in potential future positions. By joining our talent pipeline, you will be among the first to be notified when suitable opportunities arise.
We are building a network of exceptional individuals who possess the skills and experience required for future openings. By submitting your application, you will be added to our talent pipeline and considered for future opportunities.
Purpose:
Responsible for providing leadership, support, management, guidance and supervision for the Biologics group to ensure that all day to day activities of operations run smoothly and seamlessly.
Responsible for assuring that all performance metrics, workload deliverables are completed in alignment with the sites business model.
Build and maintain collaborative relationships with other team members within the site and departments.
Responsible for supporting Cell Culture, Central Services and Purification areas.
Performs general to complex duties in assigned area within the Biologics Production facility.
Complies with safety requirements, current Good Manufacturing Practices, and Standard Operating Procedures.
Organize daily and weekly shift activities and direct junior personnel in execution of daily and weekly tasks.
Responsibilities:
Operates equipment including Media Preparation, Buffer Preparation and Glass Wash/Autoclaves, bioreactors, inoculum transfers, filtration and chromatography equipment.
Performs the set-up and sterilization of components and process equipment
Monitors and adjusts equipment operation
Coordinates process sampling and routine measurements
Ensures that data is recorded, activities logged, and processes monitored appropriately
Interfaces with automated production systems and controls
Reviews records for completeness and accuracy
Authors or revises standard operating procedures
Coordinates activities in the startup and validation of new equipment or new areas
Trains junior members as a qualified/certified trainer
Communicates all events/issues with appropriate individuals
Initiates or implements changes of both physical and written procedures
Proficient in core and related work processes
Implements improvements to work processes
Knowledge of complex technical issues and manufacturing experience in a biopharmaceutical / pharmaceutical or similar environment
Requirements:
Bachelor of Science
8 - 12+ years of relevant experience
2+ years of supervisory experience in Biotechnology/Pharmaceutical Manufacturing
Strong working knowledge of Microsoft and other software packages (SAP, LIMS)
Experience with cGMP documentation and record maintenance
Strong problem solving and prioritization skills
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