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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Quality Engineer
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Senior Quality Engineer
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Director, Quality Engineering
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Supplier Quality Engineer
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Supplier Quality Engineer
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Lead Quality Engineer
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Director, Quality Engineering
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Seismic Boston, United StatesPlease be aware we have noticed an increase in hiring scams potentially targeting Seismic candidates. Read our full statement on our Career's page. · Seismic, a rapidly growing Forbes Cloud 100 company, is the global leader in enablement, helping make sales teams better by becomi ...
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Lead Quality Engineer
2 weeks ago
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Manufacturing Quality Engineer
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Associate Quality Engineer
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Software Quality Engineer
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Money Fit by DRS Boston, United StatesSoftware Quality Engineer · Job Description · BrioHealth Solutions Inc., Inc. is seeking a Software Quality Engineer to support design quality efforts for an active implantable medical device, covering both clinical and commercial needs in a GMP environment. In this role, you w ...
Quality Engineer - Boston, United States - Connect Life Science
Description
Position:
Quality Engineer
Location:
Boston – Hybrid (25% onsite)
Duration: 6 Months Contract
A medical device contract manufacturer, bringing a device to the market are seeking a Quality Engineer who is a critical thinker, data driven, and quality minded.
Job Responsibilities:
Initiate medical device quality assurance activities in accordance with (FDA 21 CFR 820, ISO 13485; and other applicable regulatory requirements).
Participate in design and drawing reviews to ensure that components meet requirements for design and patient safety requirements.
Interface and take the lead QA role in interactions with suppliers, contractors, and consultants supplying components, subassemblies, and contract processing.
Lead complaint investigations on returned product.Manage corrective action and quality improvement activities.
Lead in technical discussions with suppliers to identify and implement improvements in products and processes.
Experience:
Bachelor's Degree in Engineering or technical field with minimum 5-7 years
Experience supporting, coordinating and / or leading projects
Experience in development of new or existing medical devices
Knowledge of regulatory Medical Device regulations (FDA 21 CFR 820, ISO 13485; and other applicable regulatory requirements).
Investigation and root cause analysis skills
knowledge of change control process and project management
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