The Collections Lead is responsible for overseeing the collection efforts in accounts receivable and the supervision of the collections and cash applications staff. They will work closely with outside Collection Agencies.
The Logistics Associate is responsible for receiving and or shipping all materials including but not limited to: cGMP raw materials, NON-cGMP raw materials, Common Supply, maintenance, repair and operations (MRO) supplies, Work-in-Process (WIP), and Finished Goods Inventory (FGI).
The primary purpose of this position is to review, inspect, and disposition incoming raw materials for QA, processing of rejected lots out of inventory, processing of returned goods for QA. The secondary purpose of this job is to process document changes for material specifications and process supplier qualification documentation for new and existing suppliers
In addition to the execution of the core Reimbursement Supervisor functions listed below, the Reimbursement Supervisor is also responsible for team’s ongoing functioning and overall performance. Additional responsibilities include: research and resolution of escalated issues, assistance with training, auditing cases, effective and strong communication with the Sales Team, payer research, and completion of special projects as assigned by Associate Director. The Reimbursement Supervisor will support both RTLs and assist with tasks for either RS or RCA with minimal direction from the Associate Director to support the team. The Reimbursement Supervisor will respond to all provider account, patient, and internal inquiries in a timely fashion and document all interactions consistently. The Reimbursement Supervisor is also responsible for providing thorough evaluation of staff performance and recommending sound solutions to meet business needs.
The Chief Legal Officer oversees all legal activities for Osiris Therapeutics, Inc. This executive leader is responsible to ensure Osiris is compliant with all applicable laws specific to the life sciences/biotechnology industry, employment, and business process laws. The CLO also collaborates with other members of Osiris’ Executive Leadership on legal matters. This position reports the Chief Executive Officer.
Responsible for hands-on execution of all activities in the Biosurgery manufacturing area, which encompasses the processing and packaging of tissue products for transplantation and for use in surgical procedures. All duties are performed in compliance with GMP/GTP, American Association of Tissue Banks Standards, and Osiris Standard Operating Procedures (SOPs). The candidate should have a commitment to high standards of quality.
Manufacturing Cleaning Technicians perform routine cleaning and disinfection of the manufacturing clean rooms and supporting areas in accordance with established Standard Operating Procedures (SOPs) and all applicable regulations.
As a QCEMII you will conduct environmental monitoring (EM) according to Standard Operating Procedures (SOPs) in a cleanroom facility. Use sophisticated laboratory instrumentation and computer systems to collect and record environmental monitoring data. Process and evaluate environmental monitoring samples according to SOPs. Review and trend data for documentation of procedures and reports. Initiates and writes investigations and SOPs. Receive and ship in process and final product samples. Apply knowledge of Good Documentation Practices (GDP) and Current Good Tissue Practices (cGTP) on a daily basis.
The Associate Regional Sales Specialist is a field based position where the Specialist acts as an ambassador for Osiris Therapeutics Inc and its products. The Specialist will demonstrate and guide clientele to products that suit their patient needs. They provide information related to quality standards and compliance within the product offering and attains contracts and sales targets notably through exceptional knowledge and customer service. You will be working with and learning from our Top Sales talent in this Associate role.