| Job alert | Jobs 41 - 50 of 637 |
Instrument Laboratory Associate
T2 Biosystems
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Lexington, MA
... Experience working in an FDA-regulated environment under a quality control system a plus. Excellent organizational, recordkeeping and communication skills (verbal and written). Experience using Microsoft Office (Excel, Word, etc.) required. Must ... - Apr 21
Senior Mechanical Engineer - Sustaining Engineering
TransMedics, Inc.
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Andover, MA
... with 6 years mechanical design/engineering experience or equivalent combination of education and experience Experience with FDA, ISO, and IEC standards a plus Proven ability to develop mechanical designs using best engineering practices Must have ... - Apr 27
Senior Human Factors Engineer
Embecta
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Andover, MA
... Human Factors evidence of successful use-related risk mitigation specific to the device and its development (for both FDA and CE mark) EXPERIENCE & EDUCATION: * Bachelor's Degree in a technical field related to Human Factors Engineering (human ... - May 08
Senior Software Engineer
Cytrellis Biosystems
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Woburn, MA, 01801
... What makes Cytrellis different: ️ Unique product offering – ellacor by Cytrellis is the FIRST and ONLY FDA-cleared device for non-surgical, scarless skin removal. ️ Untapped Market Potential: 5x account growth in the last 8 months ️Voted Best Non ... - May 03
QA Complaint Coordinator
Mondo
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Bedford, MA, 01730
... Qualifications: Relevant work experience in an administrative capacity, ideally in a medical device company or similar industry Understanding of quality management systems, document control processes, and regulatory requirements (e.g., FDA, ISO ... - Apr 29
Staff Engineer, Human Factors
Embecta
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Andover, MA
... Human Factors evidence of successful use-related risk mitigation specific to the device and its development (for both FDA and CE mark) EXPERIENCE & EDUCATION: * Bachelor's Degree in a technical field related to Human Factors Engineering (human ... - May 07
Senior Validation Engineer
a Medical Devices company in MA
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Bedford, MA, 01730
... RESPONSIBILITIES Minimum 8+ years of validation experience in pharmaceutical, medical device or FDA regulated environments. Strong understanding of cGMP and regulations related to facility, utility, equipment, and process validations. Ability to ... - Apr 22
Sr. Director Toxicology
Delix Therapeutics
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Bedford, MA, 01730
... Delix is advancing these compounds through preclinical and clinical development to bring patients FDA-approved medicines that will address significant unmet needs. Headquartered in Massachusetts, Delix is building a world-class biotechnology company ... - Apr 22
Future - Genomic Expression - an RNA Diagnostic Company
Genomic Expression Inc
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Beverly, MA, 01915
... We operate a CLIA Lab in Boston and have launched COVID-19 PCR test under FDA EUA. Currently only 1 out of 4 cancer treatment prolongs life, yet we spend $100 billion on drugs and 8 million patients die every year from the disease. Genomic ... - May 10
Senior SAS Programmer
IntePros
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Cambridge, MA, 02140
... Knowledge of SDTM, ADaM, FDA and ICH guidance. Understanding of Code of Federal Regulations (CFR) Title 21, Part 11. Strong organizational and time management skills. Consistent experience as a lead statistical programmer. Excellent analytical and ... - Apr 28