|
Resume alert |
Resumes 111 - 120 of 526 |
Wakefield, MA, 01880
... High applicable knowledge and application of GD&T, ANSI Y14.5, TOL STACK, UL,EUL, IEC 60601-1, ISO13485, FDA CFR 21, ISO 6,7,8, GMP, 510k submittal process, SAP Supply Chain management, Project implementation and management, IQ,OQ, PQ, Validation ...
- 2020 Aug 14
West Newton, MA
... Key Achievements: • Updated 100 store menus with FDA regulatory calorie information within 4 months. • Reduced inventory from $100K to $25K, achieving a 75% reduction in annual costs. • Decreased printing costs 40% by switching vendors and having ...
- 2020 Aug 07
Watertown, MA
... Copied and bound documents and reports for FDA submissions, prepared correspondence and packages for mailing Filed correspondence, Device History Files and other records, entered data into the Device History Database and the QC Database, maintained ...
- 2020 Jul 15
Boston, MA
... Reimplemented proprietary insulin administration device to meet FDA approval and CE mark. Altium used as cad system during the entire process. RS485 (differential pair communications) for remote diagnostic devices when patient has attached device. ...
- 2020 Jul 08
Boston, MA
... Successfully registered products with FDA, arranged international logistics and successfully imported, warehoused and distributed product in the United States. Led all online and traditional marketing campaigns, including several televised ...
- 2020 Jul 03
Jamaica Plain, MA
... Pharmacovigilance, STED, CTA, BLA, eCTD and NDA, EU Medical Device regulations and standards Regulatory compliance knowledge of FDA IVD requirements, familiarity with QSR device design control process and understanding of IDE application and PMA ...
- 2020 Jun 24
Lynn, MA
... ● Performed tests under protocol to satisfy FDA medical device requirements. ● Prepared device documentation to be sent to the FDA and manufacturers ● Documented product issues and provided solutions ● Executed and optimized assembly process of ...
- 2020 Jun 20
Wakefield, MA, 01880
... interface with engineers, designers, and CAD vault users, providing vault training, writing reference literature, troubleshooting vault issues, etc., concerning the company’s Med device components, systems, and peripherals, to FDA & ANSI Standards. ...
- 2020 Jun 09
Lexington, MA
... Testing of software on Medical Device patient monitoring and analytical chemistry A1c chromatography instrumentation IVD (FDA regulated medical devices). Compared SAS datasets using SAS PROC Compare Developed test requirements and test plans for ...
- 2020 May 28
Acton, MA
... Evaluates, trends and reports stability data for internal use and for FDA via required periodic reports. Conduct QC review of data associated with these drug product Development activities. Coordinate the activities at various contractors to insure ...
- 2020 May 06