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FDA resumes in Northborough, MA

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Resume alert Resumes 21 - 30 of 249

Clinical Research Data Entry

Massachusetts
... will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor •The CRC I will also ensure study ... - 2023 Sep 09

Data Entry,Quality Control, Truck Driver NonCDL

Gardner, MA
... Placed April 2019 To 2021 Machine Operator Lead Quality control,FDA Paperwork, Clean and Efficient Work space, and Production Paperwork, Knowledge of Machines Controlling Systems February 2020 to March 2021 DN VAN LINES Northborough,MA. Truck Driver ... - 2023 Sep 07

Clinical Research Public Health

Newton, MA
... • Demonstrated extensive knowledge of regulatory requirements governing clinical research, including FDA regulations, Clinical Trial Management System (CTMS), Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, ... - 2023 Aug 31

Quality Assurance Supply Chain

Norwood, MA
... • Managed the reconciliation of method development and validation, GLP compliance, documentation, completeness, and compliance per FDA guidelines, following SOPs, protocols, QA compliance, and a review checklist. Academic Project • Conducted a ... - 2023 Aug 29

Electrical Engineer Project Manager

Wayland, MA
... FDA, FMEA; IEC60601, OrCAD and Altium capture. 2022 – current Senior Electrical Engineer, Gener8, Woburn MA Medical Device schematic development, BOM, prototyping, testing. 2019 – 2022 Principal Electrical Engineer, Epam Systems, Boston MA Hardware ... - 2023 Jul 03

Chief Product Officer

Hudson, MA
... Accomplishments • Developed a comprehensive digital telehealth patient engagement and analytics platform on AWS Lambda and MongoDB, integrating FDA cleared vital signs sensors with all-in-one patient mobile apps, providing a seamless and efficient ... - 2023 Jun 22

Document Reviewer Team Member

Billerica, MA
... ● Technical lead - biomarker IHC assay projects, submitted to FDA (immuno-drug conjugate assays) in support of Phase I/II clinical trials ● Wrote standard work, assay development procedures, final GLP reports. ● Authored portions of IND submissions, ... - 2023 Jun 07

Award Winning/Rare Disease/Pharmaceutical Specialist Sales

Westwood, MA, 02090
... Key Accomplishment Earned second rank salesperson in a district of 12 salespeople Radiology Imaging Specialist /Lantheus Medical Imaging/Quintiles 2009-2011 Led sales and marketing for the first and only FDA-approved MRA Blood-Pool contrasting agent ... - 2023 May 21

Director, National Security & Emergency Management

Wellesley, MA, 02482
... Experienced compliance in the GCP and FDA procedures as well as proper disposal and documentation of hazardous materials; Oversaw and procure professional contracted services including security, grounds, facility system maintenance and repair; ... - 2023 May 20

RN

Framingham, MA
... What Every Health Care Provider Should Know About Patient Safety- Published in 2018 Co-Author Chapter 46 “Equipment Sequestration”- The process for sequestering malfunctioning healthcare equipment and FDA reporting processes - 2023 May 18
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