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Resumes 1 - 10 of 620 |
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
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
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
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
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
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
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
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
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
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