4 principal qa engineer jobs at 4 companies in Boxborough, MA

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Principal Engineer, Advanced Manufacturing
Billerica, Massachusetts, United States
$150k-$200k/yr OnsiteFull Time
Boston Materials
Boston Materials: Manufactures advanced energy transfer materials for semiconductors and aerospace.
Bachelor's or master's in materials science, chemical, mechanical engineering, or related field; experience scaling materials processes into controlled manufacturing; MES, SCADA, SPC, IQ/OQ/PQ, QA/QC, and process control expertise.
Manufacturing Execution Systems (MES), SCADA, Statistical Process Control (SPC), Tulip, Ignition, JMP, Minitab, IQ/OQ/PQ
2mo
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Principal Hardware Engineer
Nashua, New Hampshire, United States
OnsiteFull Time
Geophysical Survey Systems, Inc. (GSSI)
Geophysical Survey Systems, Inc. (GSSI): Design and manufacture ground penetrating radar equipment for subsurface inspection.
15+ YOEBS in EE, 15+ years EE experience, deep analog/digital PCB and high-speed design, FPGA/VHDL/Verilog experience, full product lifecycle from concept to manufacturing, test method design, QA/root cause, and mentoring experience.
FPGA, VHDL, Verilog, Altium Designer
1mo
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Principal Software Quality Assurance Engineer
Merrimack, New Hampshire, United States
OnsiteFull Time
BAE Systems
BAE SystemsLondon Stock Exchange: BA: Provides advanced defense, aerospace, and security technology solutions.
4+ YOEBachelor's in a technical field or equivalent experience,4+ years engineering experience,active Secret clearance and ability to obtain Top Secret/SCI with polygraph,knowledge of industry standards and software QA tools,Agile/Scrum experience.
Jira, Confluence, Bitbucket, Linux, Unix, Windows, C++, Java, Python, SQL, Oracle, Scrum, 8D, Lean Six Sigma
3w
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Principal Clinical Quality Assurance Specialist
Marlborough, Massachusetts, United States
$117k-$222k/yr HybridFull Time
Boston Scientific
Boston ScientificNYSE: BSX: Developing and manufacturing innovative medical devices for less-invasive treatments.
5+ YOEBachelor's degree in science/engineering/health-related field, 5+ years clinical QA or clinical research compliance experience, 5+ years conducting GCP/regulatory audits, knowledge of ISO 14155/13485/GCP/GMP/GDP, CAPA and quality systems experience.