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FDA resumes in Boxford, MA

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Resume alert Resumes 31 - 40 of 461

Production Supervisor Data Entry

Gloucester, MA, 01930
... Performed data entry of lot numbers for food grade and medical grade gases per the FDA. Instituted a barcode system for inventory control that increased efficiency and saved money. Cabot Corporation, Haverhill, MA Production Associate Jan 2015 to ... - 2023 Oct 09

Equity Analyst

Belmont, MA
... For pharmaceutical companies I review the FDA calendar and read industry publications to identify investment candidates. I analyze Phase I, II, III studies to examine the efficacy of the drug and assess the likelihood of FDA approval. I review ... - 2023 Oct 02

Supply Chain Operations Manager

Medford, MA
... Quality and Supplier Qualifications and ISO 9001-2015 and FDA 13485 certifications audits. Persimmon Technologies Wakefield, MA June 2014 – June 2016 Senior Material Program Manager Materials Program Manager for Robotics manufacturer supporting the ... - 2023 Aug 07

Product development engineer

Lowell, MA
... Recall Technician - Temporary Nova Biomedical - Billerica, MA September 2013 to November 2013 Involved in a regulatory compliant FDA recall of blood glucose test strips. Initiated RMA log sheets by confirming consumer demographics and expected ... - 2023 Jul 21

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

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
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