Looking for a machine operator to work in gmp environment.

They must be able to use pallet jacks and it is desirable that they can use electrical pallet jacks. Responsible for performing manual and automated packaging and labeling of skeleton kits, transport tubes, penetrable caps and final kits according to schedules and GMP guidelines; also performs manual and automatic filling of lysing tubes Perform manual and semi-automated labeling of tubes, kits and kit components according to written instructions

Manufacture complex bulk formulations for diagnostic kit reagents, Responsible for sub-assembly formulation, Prepares and/or processes raw materials.

Required someone to execute assembly instructions per Batch Record requirements for Packaging and Labeling processes in compliance with cGMP guidelines.

Responsible for tracking inventory and maintaining accurate inventory records and able to research any discrepancies. Display a strong understanding of the equipment he/she uses, the location of product, and the lay-out of the warehouse, slot location, lost sales, mispicks, pack size and all other applicable product information.

Looking for a shipping and receiving clerk to work in GMP environment.

Looking for a shipping and receiving clerk to work in GMP environment.

Location-- Newark DE. Perform activities related to the timely and efficient movement of materials (receipt, handling, storage, shipment) in a fast-paced production environment. Maintain a clean and safe work environment, consistently meet productivity metrics, and adhere to all company and departmental policies. Acquires job skills and learns company policies and procedures to complete routine tasks. Normally receives detailed instructions on all work. Works under limited supervision. Works on assignments that are routine in nature, requiring limited judgment. Has little or no role in decision-making.

Location : OAK BROOK Illinois 60523. We are seeking a skilled Instructional Designer to join our team on a 6-month contract basis. The ideal candidate will have extensive experience in developing classroom-based, instructor-led training materials and must be well-versed in applying the ADDIE model. You’ll support learning initiatives across Customer Care, Revenue Management, and Billing functions.

Responsible for overseeing the design and delivery of trials within a given late phase program or multiple early-phase programs in the Immuno-Oncology group. Reports to the Medical Lead for the given program(s) and is accountable for defining the strategy and execution of assigned trials. Clinical team leader with clear understanding of areas of responsibilities and accountabilities of the role. Team player who is comfortable in situations where the role serves as a consultant and supports other functions and particularly the asset area. Understands the criticality of information and knowledge management, partnership and collaboration required in drug development.

The successful candidate will join Development Support at Client, focusing on providing a variety on non-GMP services to internal Client’s customers throughout the PO&T organization. These services include basic and complex solution preparation, media and buffer characterization, definition of assay release criteria, and deviation investigation/troubleshooting.

The role will require processing mail, data entry, and mail runs throughout the building. Candidates should be comfortable lifting up to 50 pounds on their own and pushing 400 pounds with a dolly. Assistance will be available for lifting over 50 pounds. The hiring manager is looking for candidates with experience in data entry and computer skills as they will be learning mail processing software as part of this role.