| Resume alert | Resumes 61 - 70 of 24185 |
Quality Control Team Member
Bayonne, NJ
... ● Ensuring that all research and development activities comply with regulatory requirements set by health authorities (such as the FDA in the United States). ● Monitoring the quality of pharmaceutical products throughout the development process. R&D ... - May 18
... ● Ensuring that all research and development activities comply with regulatory requirements set by health authorities (such as the FDA in the United States). ● Monitoring the quality of pharmaceutical products throughout the development process. R&D ... - May 18
Data Entry Bdc Representative
Atlanta, GA
... production -Assembly -Took daily inventory -Completed daily production forms for record keeping -Abided by and reinforced FDA regulations "Mailroom Clerk" UPS 2012 to 2013 -Packed items -Scanned images and documents - Sorted mail -Inspected ... - May 17
... production -Assembly -Took daily inventory -Completed daily production forms for record keeping -Abided by and reinforced FDA regulations "Mailroom Clerk" UPS 2012 to 2013 -Packed items -Scanned images and documents - Sorted mail -Inspected ... - May 17
Senior Software Qa
Palm Bay, FL
... My tasks involved traversing the entire UI of the device while verifying proper functionality, code reviews and submitting all paperwork that is required by the FDA. Responsible for testing APIs Set up the test and automation framework from the ... - May 17
... My tasks involved traversing the entire UI of the device while verifying proper functionality, code reviews and submitting all paperwork that is required by the FDA. Responsible for testing APIs Set up the test and automation framework from the ... - May 17
Clinical Research Manager
Cape Coral, FL, 33909
Susana Perez Martinez 502-***-**** Cape Coral, FL 33909 ad5ryq@r.postjobfree.com linkedin.com/in/susanaperezmartin3z WORK EXPERIENCE Clinical Research Manager at Argus Research Center, Inc./Tyson Eye, Cape Coral, FL 2022-Present Adhere to FDA and ... - May 17
Susana Perez Martinez 502-***-**** Cape Coral, FL 33909 ad5ryq@r.postjobfree.com linkedin.com/in/susanaperezmartin3z WORK EXPERIENCE Clinical Research Manager at Argus Research Center, Inc./Tyson Eye, Cape Coral, FL 2022-Present Adhere to FDA and ... - May 17
Quality Assurance Continuous Improvement
Cleveland, OH
... • Revised procedures to comply with ISO and FDA requirements. 08/2014 to 12/2014 Sr. Quality Manager Flambeau Inc. • Created Specifications with Customer for medical device manufacturing • Created the risk management program for medical device • ... - May 17
... • Revised procedures to comply with ISO and FDA requirements. 08/2014 to 12/2014 Sr. Quality Manager Flambeau Inc. • Created Specifications with Customer for medical device manufacturing • Created the risk management program for medical device • ... - May 17
Risk Management Quality Systems
Pasadena, CA
... managing in FDA 21CFR Parts 820, 210 and 211 Quality System Regulation, ISO 9001, ISO 14971, ISO13485, and ISO 11979 Standards, as well AS 9100 quality systems. Execute several internal and external audit functions; providing oversight role to lead ... - May 17
... managing in FDA 21CFR Parts 820, 210 and 211 Quality System Regulation, ISO 9001, ISO 14971, ISO13485, and ISO 11979 Standards, as well AS 9100 quality systems. Execute several internal and external audit functions; providing oversight role to lead ... - May 17
Pharmacy Technician
Tracy, CA
... SKILLS Customer Service POS systems Cash handling Payment processing Insurance billing Insurance Verification Organizational skills Problem-solving skills FDA compliance Pharmacy operations Data entry EXPERIENCE Cashier Tracy, CA WinCo Foods/ Dec ... - May 17
... SKILLS Customer Service POS systems Cash handling Payment processing Insurance billing Insurance Verification Organizational skills Problem-solving skills FDA compliance Pharmacy operations Data entry EXPERIENCE Cashier Tracy, CA WinCo Foods/ Dec ... - May 17
Product Development Project Management
Rochester, NY
... • Development and execution of validation plans for production equipment Clean- In-Place (CIP) and sterilization-In-Place (SIP) to meet cGMP, FDA, HACCP, FSSC 22000 and Kosher standards. • Design process, temperature and hold time conditions for ... - May 17
... • Development and execution of validation plans for production equipment Clean- In-Place (CIP) and sterilization-In-Place (SIP) to meet cGMP, FDA, HACCP, FSSC 22000 and Kosher standards. • Design process, temperature and hold time conditions for ... - May 17
Software Development Life Cycle
Atlanta, GA
... (CSA) • Computer System Validation (CSV) • Corrective Action Preventative Action (CAPA) • Design History File (DHF) • FDA 21 CFR Part 11, Part 820 • Good X Practices (GXP) • Installation Qualification (IQ) • ISO-13485 • LabLynx LIMS • LabWare ... - May 17
... (CSA) • Computer System Validation (CSV) • Corrective Action Preventative Action (CAPA) • Design History File (DHF) • FDA 21 CFR Part 11, Part 820 • Good X Practices (GXP) • Installation Qualification (IQ) • ISO-13485 • LabLynx LIMS • LabWare ... - May 17
Digital Innovation and Business Startup Executive
Knoxville, TN, 37923
... Their primary aim is to harness a unique FDA-endorsed standard to collect and understand healthcare data, making it accessible and useful for patients and medical professionals alike. A wealth of experience in technology and business marks Joe's ... - May 17
... Their primary aim is to harness a unique FDA-endorsed standard to collect and understand healthcare data, making it accessible and useful for patients and medical professionals alike. A wealth of experience in technology and business marks Joe's ... - May 17