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Resumes 11 - 20 of 32 |
Syracuse, NY
... • Held code reviews and worked on Unit Verification documents for medical features and components that needed to be documented by the FDA. • Managed and updated medical reports, tables, and stored products, across multiple portals with Visual Studio ...
- 2020 Jan 29
Liverpool, NY
... guidance to ensure all post-marketing activities associated with the company's production were in compliance with FDA's regulations and guidance Interacted with the senior management, team, and associates to facilitate smooth communication ...
- 2019 Oct 30
Auburn, NY
... Direct interaction with FDA and ISO auditors. Manage a direct staff of four senior supplier quality engineers responsible for an active supply base of over 1700 materials in commodities ranging from metal fabrication and plastic injection molding to ...
- 2018 Sep 07
Liverpool, NY
... Create validation requirements for lab equipment and administer company IT policy in compliance with FDA standards. Oversee company IT inventory and supplies.
- 2017 Oct 14
Canastota, NY, 13032
... Established and maintained reports and documentation to meet FDA regulations. Bought and sold supplies and products necessary to run the dairy farm. Met 100% of budget requirements and instituted cost saving yearly. Collaborated with several ...
- 2017 May 18
Syracuse, NY
... All work done in compliance with ISO documentation and FDA standards / requirements. Designed packaging for x-ray software (Digital Fluoroscopy, Cardiology, Angiography, Radiography) to rebrand product for new product launch into international ...
- 2017 Feb 07
Onondaga County, NY
... Various codes, regulations and guidelines, OSHA safety and HAZMAT regulations, direct interaction with NYSDOH, DEC, DEP, NYSDOL, USDOL, EPA, FDA, DOD, DOE, DOT, HUD, USDA, FAA, NRC, Home Land Security, Army Corp of Eng, with regard to local, state ...
- 2015 Aug 19
Liverpool, NY
... • Prepared status reports, test result reports, problem logging spreadsheets • Software Verification and Validation based on FDA Software V & V guidelines • Reported project status and project estimates to the Software Test Engineer Lead and Project ...
- 2015 Mar 12
Syracuse, NY
... *Responsibility of ensuring that daily activities, including the release of incoming and finished products, meet GMP standards and specifications as well as to conform to FDA regulations. *Enforce standard operating procedures were followed ...
- 2013 Dec 16
Liverpool, NY
... Strong additional experience in production line supervision, hands on system maintenance and troubleshooting, environmental compliance, pharmaceutical validation, FDA cGMP compliance, safety, procurement, and quality control. Accomplishments ...
- 2013 Jan 02