| Resume alert | Resumes 1 - 10 of 620 |
Quality Assurance Public Health
Chicago, IL
... 2015 – May 2016 Quality Coordinator HACCP Training, GMP Training, Food Safety training, FDA Food Regulations Training, and Allergen Training for food defense plans for airlines and railways Coordinate completion of Corrective Action Preventive ... - Jun 20
... 2015 – May 2016 Quality Coordinator HACCP Training, GMP Training, Food Safety training, FDA Food Regulations Training, and Allergen Training for food defense plans for airlines and railways Coordinate completion of Corrective Action Preventive ... - Jun 20
Executive Assistant United States
Chicago, IL
... ●Conducted compliance audits (HIPAA), OSHA, FDA, HACCP, cost control, completed corrective actions, vendor management, and restructured performance improvement programs for business operations ●Implemented strict budget commitments, financial ... - Jun 14
... ●Conducted compliance audits (HIPAA), OSHA, FDA, HACCP, cost control, completed corrective actions, vendor management, and restructured performance improvement programs for business operations ●Implemented strict budget commitments, financial ... - Jun 14
Project Manager Medical Device
Lincolnshire, IL, 60069
... Experienced in Quality, Hip, knees, Femoral, R&D, Packaging, Manufacturing, Inventory and calibration departments, Specialist with a demonstrated history of working in the medical device industry / FDA 21 CFR11, 21 CFR820, ISO 9001, ISO 13485, ... - Jun 13
... Experienced in Quality, Hip, knees, Femoral, R&D, Packaging, Manufacturing, Inventory and calibration departments, Specialist with a demonstrated history of working in the medical device industry / FDA 21 CFR11, 21 CFR820, ISO 9001, ISO 13485, ... - Jun 13
Technical Writer Business Analyst
Skokie, IL
... This included EPA disposal regulations, a scientific term glossary, and FDA regulated procedural manuals. Solution Partners - Pfizer Lake Forest, Illinois June 2017 – December 2018 Technical Writer/Business Analyst Responsibilities included the ... - Jun 12
... This included EPA disposal regulations, a scientific term glossary, and FDA regulated procedural manuals. Solution Partners - Pfizer Lake Forest, Illinois June 2017 – December 2018 Technical Writer/Business Analyst Responsibilities included the ... - Jun 12
Project Manager Management
Lincolnshire, IL
... ● Participated in FDA inspections and client audits. ● Focused on continuous improvement initiatives: quality, safety, data integrity, operational excellence, efficiency, technical expertise, advanced technologies, and new service offerings. Key ... - May 30
... ● Participated in FDA inspections and client audits. ● Focused on continuous improvement initiatives: quality, safety, data integrity, operational excellence, efficiency, technical expertise, advanced technologies, and new service offerings. Key ... - May 30
Quality Assurance Data Analyst
Elk Grove Village, IL
... based on input ●Selected to implement and lead efforts to broaden RWS machine language translation functionality in Veeva RIM, including creating validation test cases, new SOPs for FDA ICH submissions, and product-labeling translation requests; ... - May 30
... based on input ●Selected to implement and lead efforts to broaden RWS machine language translation functionality in Veeva RIM, including creating validation test cases, new SOPs for FDA ICH submissions, and product-labeling translation requests; ... - May 30
Mental Health Social Worker
Chicago, IL
... Enter Data into EDC and answer Queries per FDA guidelines and review them against the subject's medical record for completeness and accuracy. ●Ensure the filing and maintenance of all regulatory documents and files at the study site. ●Train back-up ... - May 22
... Enter Data into EDC and answer Queries per FDA guidelines and review them against the subject's medical record for completeness and accuracy. ●Ensure the filing and maintenance of all regulatory documents and files at the study site. ●Train back-up ... - May 22
Clinical Study Medical Writer
Chicago, IL
Therese M De Serto Cohen Summary: More than ** years of experience as a technical/Medical writer, Pharmaceutical Industry: Phase I – 4 IND/NDA/PMO/IRB/FDA/WHO submissions, all documents and processes associated with conducting GCP/GMP studies from ... - May 15
Therese M De Serto Cohen Summary: More than ** years of experience as a technical/Medical writer, Pharmaceutical Industry: Phase I – 4 IND/NDA/PMO/IRB/FDA/WHO submissions, all documents and processes associated with conducting GCP/GMP studies from ... - May 15
Quality Assurance Control
Chicago, IL
... Knowledgeable on FDA and other regulatory entities procedures that are required to follow in order to sell and produce edible baked goods for human consumption for profit. S.T. Specialty Foods 1/2013 – 12/2016 Senior Quality Assurance Specialist ... - May 13
... Knowledgeable on FDA and other regulatory entities procedures that are required to follow in order to sell and produce edible baked goods for human consumption for profit. S.T. Specialty Foods 1/2013 – 12/2016 Senior Quality Assurance Specialist ... - May 13
Quality Management, Continuous Improvement, Lean / Six Sigma
Chicago, IL
CONTACT: Homewood, IL ad5jor@r.postjobfree.com 815-***-**** www.linkedin.com/in/richard- santoro-cssbb-tqmp-2346593 SPECIALTIES: Quality Management System & Compliance FDA GMP Medical Device & Pharmaceutical Regulations EU MDR, Health Canada SOR/98 ... - May 07
CONTACT: Homewood, IL ad5jor@r.postjobfree.com 815-***-**** www.linkedin.com/in/richard- santoro-cssbb-tqmp-2346593 SPECIALTIES: Quality Management System & Compliance FDA GMP Medical Device & Pharmaceutical Regulations EU MDR, Health Canada SOR/98 ... - May 07