- Kedplasma (Springfield, IL)
- …suitability and handling donor reactions under the direction of the Center Manager , Physician Substitute Supervisor and Center Medical Director. Operates within the ... scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...and meeting(s) in a timely manner as instructed by supervisor/ manager . + Cooperate with department personnel, as well as… more
- Fujifilm (Springfield, IL)
- …. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements , applicable ISO 13485 standard requirements ... on systems within a service area as directed by the Area Service Manager . **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to… more
- Kedplasma (Chicago, IL)
- …Responsible for registering and screening donors under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice ... and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...and meeting(s) in a timely manner as instructed by supervisor/ manager . + Cooperate with department personnel, as well as… more
- Abbott (Abbott Park, IL)
- …cleaning techniques. + This position requires the individual to ensure that all regulatory requirements are met and maintained to include FDA , GMP, OSHA, INTC, ... + Operating under the general guidance of the section manager , the duties of this position include but are...and conflicting demands. + The supervisor must also determine requirements for new and replacement tools, provide training and… more
- Ace Hardware (Oak Brook, IL)
- …for this role must be well experienced in classification and PGA compliance requirements . The person will also perform basic US import entry audits. **What You'll ... to Trade Regulations** + Determine tariff classification and PGA ( FDA , Aphis, EPA, etc.) applicability. + Have working knowledge...entry audits for accuracy. + Work with Import Compliance Manager to address audit results and corrections. + Ensure… more
- ADM (Decatur, IL)
- …analytical results in a timely matter. + Support and comply to all applicable FDA , GMP, USP, Biosafety, and OSHA requirements . + Follow laboratory standards and ... applications, and software). + Maintain awareness and adhere to all applicable FDA , GMP, USP, Biosafety, OSHA and employer standards and guidelines. + Follow… more
- Highmark Health (Springfield, IL)
- …and testing processes in partnership with the pharmacy benefits manager . The successful candidate will possess excellent communication, analytical, and ... a fast-paced and collaborative environment. **ESSENTIAL RESPONSIBILITIES** + Monitor FDA -approvals, drug manufacturer pipelines, assess drug utilization reports, and… more
- Medtronic (Chicago, IL)
- …additional overnight or occasional flight travel. + Understands and adheres to FDA Regulations, quality and training requirements , SOPs, and Work ... levels at customer accounts. + Educate customers on inventory management requirements including care and handling, inventory level maintenance, Use-by-Date reviews,… more
- BioLife Plasma Services (Harwood Heights, IL)
- … (in state of licensure) for basic IV therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years ... customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to… more
- BioLife Plasma Services (Rockford, IL)
- … (in state of licensure) for basic IV therapy + Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist + Two years ... customer service and quality is expected. You will report to the Plasma Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to… more