The Manager, Supply Chain - Warehouse , reporting to the Director, Supply Chain, has an opportunity to make a significant impact on the way that Harman’s site operates. The Manager, Supply Chain - Warehouse will lead a shift consisting of Warehouse Materials Control Associates and Materials Services Associates. Responsibilities include project participation, dashboarding, reporting, and governance. The scope includes all continuous improvement initiatives related to supply chain assets, workflow processes and operations. The ability to work efficiently and partner with other functional leads to improved operational performance and compliance will be a success factor for this role.
Sr Specialist, Client QA
The Manufacturing Scheduler will report to the Senior Manager, Production Scheduling through the Supply Chain organization. This Manufacturing Scheduler will lead the entire manufacturing scheduling process for an assigned production area and will be the central source of information. As part of the Ready-to-Execute (RTE) team, this role will shape the operating model for the world’s largest cell and gene therapy manufacturing site. The goal of RTE -also referred to as “Manufacturing Readiness”- is on-time start success for planned campaigns.
The Engineer II, Manufacturing, Sciences, and Technology (MS&T) will support GMP manufacturing operations as the floor supports rapid response of manufacturing operation in upstream, downstream and drug product. On-The-Floor Engineer is actively engaged with the manufacturing team in resolving process related issues an provide immediate resolution in collaboration with quality assurance or a cross functional team. Implementation of cGMP processes. The individual will serve as a subject matter expert (SME) for biologic Upstream/Downstream Processes. Success in this position requires the ability to work hands on in a cleanroom, and the ability to collaborate in a cross-functional, fast paced environment.
Technician I, Central Services
The Scientist, QC Analytical is responsible for supporting analytical testing in order to support GMP manufacturing for both clinical and commercial clients. The Scientist, QC must demonstrate technical knowledge, be familiar with basic scientific/regulatory principles, possess initiative, and maintain a strong commitment to scientific excellence.
Technician III, Central Services
We\'re hiring a 2nd Shift Associate III, Manufacturing role to support the Fill Finish team for our pharmaceutical manufacturing facility in Baltimore, Maryland.
Technician I, Central Services
Engineering Technician
Supervisor, Manufacturing
