Distance: |
Resume alert |
Resumes 361 - 370 of 25486 |
Lithonia, GA, 30058
... • Manage assigned investigational sites to assure adherence to protocol, FDA regulations, and ICH GCP guidelines. • Perform pre-study visits to help identify adequate study sites that have the resources and facilities to conduct the clinical study. ...
- Jun 11
Lafayette, CA, 94549
... FDA-related computer systems validation methodologies, Veeva Platform Assisted in preparation of test scripts for presentation to QA for approval Worked with SFDC for data tracking, workflow optimization and user interface navigation Worked with ...
- Jun 11
Colton, CA
... DISHWASHER FIVE STAR WAREHOUSE SEPTEMBER 2014 – JANUARY 2016 · Responsible of keeping the back of house organized & cleaned by FDA safety standards · Knowledge of the three compartment sink such as proper detergent, sanitize agents & other cleaning ...
- Jun 11
Dandridge, TN, 37725
... Directed safety operations and maintained clean work environment to adhere to FDA and OSHA requirements, as well as ensure compliance for local health department regulations. Ensured compliance with applicable laws, regulations and industry ...
- Jun 10
Chesapeake, VA
... Food and Drug Administration (FDA) Supervisory Human Resource Specialist 2012 – 2016 • Strategic Hiring Initiatives: Managed recruitment for highly specialized roles, including senior executives and technical experts, ensuring alignment with FDA’s ...
- Jun 10
Mountain View, CA
... ● CRO contact to medical companies pursuing 1) Class II FDA 510(k) device and supporting software, 2) cognition and exercise studies, 3) biobanking of specimens, 4) online neurological tests, and 5) point-of-care STD tests. ● Managed creation and ...
- Jun 10
Atlanta, GA
... Engineer, Innovation Associates, 2024 - 2024 ● Designed and implemented robotic automation solutions tailored to pharmaceutical manufacturing environments, ensuring compliance with regulatory standards such as FDA cGMP guidelines and ISO 13485. ...
- Jun 10
Taunton, MA
... Electrochem Solutions(Greatbatch) 3/2012-5/2015 Senior Product Development Engineer/Project Manager: ●Responsible and accountable for the coordinated management of multiple class 2 and 3 medical device development projects for FDA approval directed ...
- Jun 10
Brookston, IN
... Worked with outside Vendors to source equipment, software and other IT related needs Maintained SOX, FDA compliance Indiana Packer’s Corporation, Delphi, Indiana Dec 2011 – May 2014 SQL / Infrastructure Manager Provided IT infrastructure leadership ...
- Jun 10
Fairfield, CA
... Involved in all aspects of the computer systems validation lifecycle, to comply with FDA 21 CFR Part 11, Part 809; Part 820; Part 830, Annex 1, Annex 11 GMP and GxP regulations. Performed Periodic reviews for the label printers, Plate Readers, and ...
- Jun 10