- Rush University Medical Center (Chicago, IL)
- …position. Offers may vary depending on the circumstances of each case. **Summary:** The Manager of Quality, Bone Marrow Transplant is serves as a member of the Bone ... medicine and/or cellular therapy. * Experience with FACT, CAP, AABB and/or FDA inspections. * Experience in quality assessment, process improvement and project… more
- US Tech Solutions (North Chicago, IL)
- …Assurance (PMQA) Analyst I will investigate and maintain **complaint files,** in compliance with regulations established by the FDA and international regulatory ... bodies, and submit safety reports to the FDA and international Competent Authorities. + In addition will...+ The candidate must conduct their work activities in compliance with all internal requirements and with all applicable… more
- Kedplasma (Chicago, IL)
- …are followed by center personnel under the direction of the Quality Assurance Manager . Escalates any non- compliance that affects donor safety or plasma quality ... of EU Guidance on Good Manufacturing Practice (GMP) and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has...their supervisors. + Provides accurate reports of the facility's compliance to Quality Assurance Manager (QAM), Regional… more
- Biomat USA, Inc. (Chicago, IL)
- …employees and supervise donor flow. * Learn and maintain thorough familiarity and compliance with all state and federal regulations, US Food and Drug Administration ... ( FDA )-approved Standard Operating Procedure Manual, Occupational Safety and Health...is performed. * Under the guidance of the Center Manager and/or the Assistant Manager , assure facility… more
- CSL Plasma (Chicago, IL)
- …facility compliance with CSL procedures and policies, cGMP, OHSA, FDA , and other regulations, as applicable, and develop center responses for deficiencies. ... **The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall … more
- Kedplasma (Springfield, IL)
- …atmosphere, ensuring compliant plasma collections 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...the position. **MAIN DUTIES AND RESPONSIBILITIES** **Core** + Ensures compliance of all plasma collection center activities with SOPs… more
- Kedplasma (Urbana, IL)
- …procedure and plasma collection, including donor set-up, monitoring and disconnect in compliance with Standard Procedures and FDA guidelines, as needed. + ... and screening donors under the direction of the Center Manager . Operates within the scope of EU Guidance on...scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has… more
- ADM (Decatur, IL)
- …results in a timely matter. + Support and comply to all applicable FDA , GMP, USP, Biosafety, and OSHA requirements. + Follow laboratory standards and maintain ... compliance with ISO 17025:2017. **Job Responsibilities:** + Prepare and...software). + Maintain awareness and adhere to all applicable FDA , GMP, USP, Biosafety, OSHA and employer standards and… more
- Kedplasma (Springfield, IL)
- …Training Manager for training-related initiatives. + Demonstrates competence and compliance with KEDPLASMA SOPs and KEDPLASMA Training Manual. + Understands and ... plasma collection center under the direction of the Center Manager . Operates within the scope of EU Guidance on...scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB SUNCTIONS** Every effort has… more
- Conagra (Chicago, IL)
- …legal department. + Meaningful experience advising on food law/regulatory matters, including FDA and USDA regulatory compliance and enforcement matters. + ... Regulatory Affairs, R&D, Labeling, Nutrition) on the full scope of food law-related compliance activities, with a particular focus on food safety, food science, and… more