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FDA resumes in Peabody, MA

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Resume alert Resumes 41 - 50 of 495

Customer Service Call Center

Amesbury, MA
... Documented all procedures per ISO and FDA requirements. Corning OFC, Natick, MA 10/99-4/01 Optical Test Technician (Quality Control) Characterized and qualified optical filters. Maintained test station calibration. Documented performance data, and ... - 2023 Jul 11

Drug Safety Specialist

Boston, MA
... ● Process Individual Case Study Reports (ICSR) and serious adverse event (SAE) reports including case intake, duplicate check, data entry, generation of narratives, MedDRA coding, quality checks, submissions to FDA through gateway; ● Submission of ... - 2023 Jul 10

Quality Assurance Set Up

Somerville, MA
... Ensure strict compliance with quality system regulations 21 CFR 820, ISO 13485 / 9001, current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), Food and Drug Administration (FDA), OSHA, and ... - 2023 Jul 10

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

Protein purification process operation

Boston, MA
... Process Support & Development Scientist, Biologics Technical Operations, Specialty Products Division, Abbott Laboratories, North Chicago, IL 1999 to 2005 • Performed process validation and justification studies to meet FDA requirements. • Supported ... - 2023 Jun 22

Chief Product Supply Officer

Boston, MA, 02109
... A hands-on executive that has significant FDA, international manufacturing, engineering, quality, procurement, distribution & fulfilment, turnaround and hypergrowth experience. Extensive experience working with boards and generating funding. ... - 2023 Jun 16

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

Safety Specialist Regulatory Affairs

Boston, MA
... I worked for QA, gap analysis, and validation, with a strong focus on ensuring compliance with FDA regulations. I am now seeking a role as a Regulatory Affairs Associate in the biotechnology and medical device industries where I can leverage my ... - 2023 Jun 01

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

Regulatory Affairs Quality Supervisor

Malden, MA
... Studies, Boston, USA Jan 2021 – Dec 2022 MS in Regulatory Affairs for Drugs, Biologics, and Medical Devices Relevant Coursework: FDA Pharmaceutical and Medical Device Regulations, Pharmaceutical Engineering, Pharmaceutical and Medical Device Law, ... - 2023 Apr 17
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