Lead Biotechnologist (Upstream)

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: Operations and Technical • Demonstrates ownership of upstream-specific operation area, including Inoculation, Cell Culture and Recovery • Plans and executes manufacturing operations using validated programs (such as LIMS, SAP, DeltaV, POMSnet, automated control systems, etc.) • Completes manufacturing tasks efficiently • Demonstrates high degree of initiative to resolve issues • Makes recommendations for and implements new procedures • Acts independently to determine methods and procedures on new assignments • Drives projects and innovations to streamline processes and operation steps • Drives the resolution of anomalous processing events timely • Initiates Demand Work Order Safety • Ensured safe work environment in accordance with regulatory and global/local EHS policies • Reinforces importance of safety during critical operations and ensure that Positive Interventions and recommendations are regularly highlighted and acted upon. • Leads safety risks assessments or participates in process hazard analysis as an operations representative (PHA) Quality • Responsible for the completeness and accuracy of all records • Ensures that all batch related document errors are resolved in a timely manner to avoid batch review and release delays • Communicates all events/issues effectively with relevant stakeholders • Drive performance to ensure execution is carried out flawlessly to ensure Human Error related events are prevented • Responsible for overall plant upkeep during the shift and ensuring plant is always in audit ready mode • Is involved in preparation for regulatory audits and inspections • Initiates Quality Records (Non-conformance) Schedule • Assists supervisor in planning to ensure adequate resources are available to support manufacturing demands per production schedule. • Assigns tasks within the shift team to biotechnologists • Provides inputs to supervisor and manufacturing planner in events of unplanned downtimes • Represents the shift in cross-functional meetings People and Culture • Sets a positive team environment and exemplifies the AbbVie Ways We Work behaviors • Coaches and trains other biotechnologists (100% trainer competency) • Assists in developing training materials • Bachelors in Sciences (i.e. Biologicals, Biomedical, Chemistry, Life Sciences, Pharmaceutical), Pharmacy, or Engineering (i.e. Biomedical, Chemical, Pharmaceutical), or equivalent  • Min 5+ years of relevant work experience in Biologics / Pharmaceutical industry required. Experience should include 3+ years of area / upstream specific experience, including Inoculation, Cell Culture and Recovery • Experience leading a shift team required • Highly skilled specialist and strong problem solver who independently tackles complex assignments with initiative, contributing to the development of innovative concepts and techniques • Demonstrated ability to multi-task and work in a fast-paced environment, takes full ownership of tasks assigned and acts with personal integrity  • Knowledge of complex technical issues and manufacturing expe