- Actalent (Maryland Heights, MO)
- …and international regulatory agencies and guidelines, such as FDA, EU, HC, TGA, PIC/S, ISO , USP, NRC, and cGMP. PAY - $29 Responsibilities + Conduct thorough and ... efficient review and disposition of completed batch record documentation, ensuring adherence to Good Documentation Practices, cGMPs, and applicable local procedures. + Perform and oversee Quality Assurance On The Floor tasks, including AQL inspections,… more
- Amentum (Fallon, NV)
- …+ Hazardous Waste Communications Training, + FOD and TCP Awareness Trained + ISO 9001-2000 Program Awareness + Operational Risk Management (ORM) Training + Position ... requires shiftwork in addition to scheduled and unscheduled overtime and weekend/holiday work. + Ability to walk and stand on level and/or inclined surfaces for extended periods throughout the day. + Ability to climb, bend, stoop, squat, crawl, crouch, kneel,… more
- Actalent (St. Paul, MN)
- …actions. + Author and execute test and validation protocols to comply with ISO and FDA medical device regulation requirements. + Verify documents are correctly ... filled out prior to set-up sign-off. + Provide training and coaching to peers and Process Technicians. + Maintain and promote a safe and clean working environment. + Follow all applicable safety procedures and guidelines as outlined in the company safety… more
- Actalent (South Portland, ME)
- …development implementation and effectiveness of the Quality Management System per ISO FDA and other regulatory agencies. + Responsible for exhibiting professional ... behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices. BASIC QUALIFICATIONS EDUCATION: + Bachelors Degree in Biology Chemistry Biochemistry Engineering or… more
- Actalent (Maple Grove, MN)
- …multiple priorities. Additional Skills & Qualifications + Experience with IEC -1 and ISO Risk Management for Medical Devices. + Proficiency in using electrical tools ... such as oscilloscopes and circuit testing equipment. + Experience with ERP systems, optical inspection, and validation processes. Work Environment The position is primarily office-based at Maple Grove, with most time spent on designing or handling customer… more
- Kelly Services (Seattle, WA)
- …escalate issues upward. + Ensures compliance with lab regulatory agencies (GxP, FDA, ISO ). + Keeps accurate and detailed records for all workflows following Good ... Documentation Practices. + Demonstrates excellent clinical judgment and integrity by possessing deep knowledge/skills in a range of laboratory procedures and processes. + Explains technical information within the team clearly and effectively. + Demonstrates… more
- Aerotek (Elk Grove Village, IL)
- …and procedures. + Work according to company Work Instructions, Policies, and ISO /AS quality standards. + Communicate production information such as quality issues ... and problems to relevant personnel. + Participate in skill development and process improvement activities. + Follow all written and oral instructions. + Resolve day-to-day issues through effective teamwork. + Accept and complete other duties to meet company… more
- Eaton Corporation (Richmond, VA)
- …and test process improvement activities, including Eaton QMS implementation, regular ISO 9001 internal/external audits and related activities. + Support testing ... function in achieving customer expectations, financial performance, and key operational performance indicators (safety, quality, delivery, cost, inventory) + Support continuous improvement activities, cost out, kaizen, business process improvement, rapid… more
- ManpowerGroup (St. Petersburg, FL)
- …labels are used during production + Support company programs such as 5S, ISO , Preventive Maintenance, and GMP standards **Qualifications:** + High School Diploma or ... GED (required) + 6+ months of manufacturing or machine operation experience (required) + Ability to work independently and demonstrate attention to detail + Physical ability to perform manufacturing tasks and handle materials up to 50 lbs (team lift required… more
- Actalent (Miami, FL)
- …tools and inspection methods. + Ensure all inspection tools and processes comply with ISO 13485 and FDA 21 CFR 820. + Follow internal design control, validation, and ... tooling management procedures. + Support internal and external audits related to inspection and measurement systems. Required Qualifications + Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, or related field. +… more