Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.
Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Quick apply
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Quick apply
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA Employment Type: Full-Time / Contract Pay Rate: $19 ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Santa Rosa, CA · On-site
$22 - $24/hr
Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly ... Collaborate with supervisors, engineers, and technicians to resolve line issues and suggest ...
Santa Rosa, CA · On-site
$22 - $24/hr
Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly ... Collaborate with supervisors, engineers, and technicians to resolve line issues and suggest ...
Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Lifecycle Engineer Location: Blue Ash, OH Duration: 6 Months Contract We are seeking an experienced Senior Medical Device Lifecycle Engineer to lead product lifecycle and ...
Blue Ash, OH · On-site
$96K - $131K/yr
Senior Medical Device Lifecycle Engineer Location: Blue Ash, OH Duration: 6 Months Contract We are seeking an experienced Senior Medical Device Lifecycle Engineer to lead product lifecycle and ...
Support and manage Design History File (DHF) activities for medical device projects. * Review ... Review engineering documents for completeness, accuracy, and compliance with quality system ...
Support and manage Design History File (DHF) activities for medical device projects. * Review ... Review engineering documents for completeness, accuracy, and compliance with quality system ...
Recruiter-Medical Device Engineering Job Title: Engineering / Medical Devices Recruiter Location: Permanent Remote Shift: 7:00 PM - 4:00 AM IST Experience: 6 months to 2 years in US Staffing ...
Recruiter-Medical Device Engineering Job Title: Engineering / Medical Devices Recruiter Location: Permanent Remote Shift: 7:00 PM - 4:00 AM IST Experience: 6 months to 2 years in US Staffing ...
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San Clemente, CA · On-site
$22.10/hr
Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...
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San Clemente, CA · On-site
$22.10/hr
Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Quick apply
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Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
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Lake Forest, CA · On-site
$20 - $21/hr
Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ... Medical device manufacturing experience preferred; 2+ years is highly desirable. * Experience in an ...
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Lake Forest, CA · On-site
$20 - $21/hr
Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ... Medical device manufacturing experience preferred; 2+ years is highly desirable. * Experience in an ...
Roseville, MN · On-site
$100K - $115K/yr
... Engineer in a regulated industry, preferably medical devices. * Experience with FDA regulations, ISO 13485, and other medical device quality standards. * Proficiency in quality tools and ...
Quick apply
Roseville, MN · On-site
$100K - $115K/yr
... Engineer in a regulated industry, preferably medical devices. * Experience with FDA regulations, ISO 13485, and other medical device quality standards. * Proficiency in quality tools and ...
Be Seen First
Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Quick apply
Be Seen First
Temecula, CA · On-site
$19.25 - $23.33/hr
Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...
Arvada, CO · On-site
$19.50 - $21/hr
Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Collaborate closely with engineering, quality, and operations teams. * Take ownership of your work ...
Arvada, CO · On-site
$19.50 - $21/hr
Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Collaborate closely with engineering, quality, and operations teams. * Take ownership of your work ...
This role focuses on supporting Design History File (DHF) activities for medical device development projects, ensuring compliance with regulatory and quality system requirements. The engineer will be ...
This role focuses on supporting Design History File (DHF) activities for medical device development projects, ensuring compliance with regulatory and quality system requirements. The engineer will be ...
Eden Prairie, MN · On-site
$18.25 - $22.50/hr
The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...
Eden Prairie, MN · On-site
$18.25 - $22.50/hr
The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...
Strong understanding of medical device product development and design control principles. * Excellent verbal and written communication skills, with the ability to train and support engineers at all ...
Quick apply
Strong understanding of medical device product development and design control principles. * Excellent verbal and written communication skills, with the ability to train and support engineers at all ...
Arvada, CO · On-site
$19.50 - $21/hr
Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Collaborate closely with engineering, quality, and operations teams. * Take ownership of your work ...
Arvada, CO · On-site
$19.50 - $21/hr
Medical Device Production Assembler Build Products That Help Change Lives Arvada, CO | Full-Time ... Collaborate closely with engineering, quality, and operations teams. * Take ownership of your work ...
Roseville, MN · On-site
$100K - $115K/yr
... Engineer in a regulated industry, preferably medical devices. * Experience with FDA regulations, ISO 13485, and other medical device quality standards. * Proficiency in quality tools and ...
Quick apply
Roseville, MN · On-site
$100K - $115K/yr
... Engineer in a regulated industry, preferably medical devices. * Experience with FDA regulations, ISO 13485, and other medical device quality standards. * Proficiency in quality tools and ...
Eden Prairie, MN · On-site
$18.25 - $22.50/hr
The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...
Eden Prairie, MN · On-site
$18.25 - $22.50/hr
The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...
$12.02 - $17.18
4% of jobs
$17.18 - $22.33
9% of jobs
$26.04 is the 25th percentile. Wages below this are outliers.
$22.33 - $27.49
17% of jobs
$27.49 - $32.65
13% of jobs
The median wage is $35.66 / hr.
$32.65 - $37.81
13% of jobs
$37.81 - $42.96
10% of jobs
$42.96 - $48.12
9% of jobs
$49.09 is the 75th percentile. Wages above this are outliers.
$48.12 - $53.28
9% of jobs
$53.28 - $58.44
7% of jobs
$58.44 - $63.59
6% of jobs
$63.59 - $68.75
4% of jobs
$12
$39
$68
For Medical Device Programmer jobs, the most frequently searched job titles are:
Blue Ash, OH • On-site
$96K - $131K/yr
Other
Posted 10 days ago
Role: Senior Medical Device Engineer PLM / Lifecycle Management
Location: Blue Ash, OH
Duration: 6+ Months Contract
Job Description:
7+ years of engineering experience in medical device or other regulated industries.
Experience leading cross-functional technical projects. Experience with component development, supplier qualification, design verification, and manufacturing validation.
Strong understanding of design controls, change management, risk management, process validation, and quality system compliance.
Must Have Technical/Functional Skills:
Strong expertise in Medical Device Product Lifecycle Management (PLM), Design Controls, and Engineering Change 5Management (ECO/ECN/ECR).
Hands-on experience with Design Verification & Validation (V&V), test methods, protocol development, and technical documentation.
Deep understanding of Risk Management methodologies, including ISO 14971, DFMEA, PFMEA, and hazard analysis.
Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory compliance requirements.
Experience in Supplier Quality Engineering, component qualification, supplier development, and Design for Manufacturability (DFM). Proficiency in Process Validation activities including IQ/OQ/PQ, pilot builds, validation builds, and manufacturing transfer. Ability to interpret engineering drawings, GD&T, tolerance stack-ups, specifications, and acceptance criteria. Strong root cause analysis and problem-solving skills utilizing 8D, CAPA, 5 Why, Fishbone, and corrective action processes. Excellent project management skills, including planning, scheduling, risk management, stakeholder management, and cross-functional coordination. Effective leadership, communication, and influencing skills, with the ability to drive decisions and deliver results without direct authority.
Roles & Responsibilities:
Lead multiple high-priority lifecycle change projects from concept through implementation.
Drive project plans, timelines, risk mitigation strategies, and implementation readiness.
Coordinate cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain, Procurement, Operations, and external suppliers.
Serve as the technical interface with suppliers for component development, DFM reviews, tooling readiness, process capability, and component qualification.
Support design verification and validation activities, including test planning, execution, data review, and technical documentation.
Partner with manufacturing sites on process validation activities, including IQ/OQ/PQ, pilot builds, validation builds, and production launch readiness.
Apply strong knowledge of design controls, engineering change management, risk management, quality system requirements, and regulatory expectations.
Review engineering drawings, specifications, GD&T requirements, tolerance analyses, and component acceptance criteria.
Drive root cause analysis, technical problem solving, and timely closure of project issues.
Education: At least a bachelor s degree (or equivalent experience) in Computer Science, Software/Electronics Engineering, Information Systems, or closely related field is required
