quality engineer medical device

CommonSpirit Health

<div><b>Job Summary and Responsibilities</b><div><br>
The CE Medical Device Network Engineer II will use the latest technology and testing analysis activities to ensure security measures are implemented throughout the entire medical device life cycle. They will successfully integrate medical device security systems and tools with the existing environment. In addition, this role partners with other Clinical Engineering technicians within the region to complete medical device related work efforts and projects that are of medium to high complexity. The Clinical Engineering (CE) Medical Device Network Engineer II works in conjunction with the Clinical Engineering Medical Device Security (CE MDS) Team for the development and implementation of remediation documentation. They have joint responsibility for maintaining and enhancing the security posture for CommonSpirit Health's medical devices, networks and information. Additionally they work directly with vendors to manage device vulnerabilities. They are jointly responsible for design, implementation and support of the Clinical Engineering IT environment. They will design, develop, configure and implement solutions to resolve technical and business issues of medium to high complexity related to medical device security. This position provides specialized repair (Radiology, Clinical Engineering and Clinical Engineering network devices) and maintenance services to medical treatment and diagnostic equipment.</div><div></div><div><br>
Essential Functions</div><ul><li>
All associated Job responsibilities of the Clinical Engineering Medical Device Network Engineer I.</li><li>
Collaborate with cross-functional teams to architect solutions that strengthen security controls of network connected medical devices without disrupting device integrity or patient safety (e.g. network architecture, active directory, group policies, windows images, end point security tools, etc.)</li><li>
Tests configurations and deploys risk mitigation strategies in known and some unknown environments.</li><li>
Prepares, documents and presents detailed guidance for system configuration and risk mitigation.</li><li>
Detects, identifies and resolves vulnerabilities in devices or systems.</li><li>
Maintains thorough documentation and completes backups.</li><li>
Resolves technical challenges and provides support to field technicians utilizing innovative solutions.</li><li>
Troubleshoot and assist with recovery of medical devices due to issues associated with upgrades, patching, security vulnerabilities, threats, etc. Collaborates with the MDS team for the development and implementation of security remediation solutions associated with medical devices within the assigned region.</li><li>
Collaborates with vendors to manage device cyber vulnerabilities</li><li>
Coordinate efforts for medical device patching and updating firmware and/or applications appropriate for the medical device.</li><li>
Research medical device manufacturer's resources for approved patches and updates applicable to medical devices in all modalities</li></ul><div>
The job summary and responsibilities listed above are designed to indicate the general nature of the work performed within this job. They are not designed to contain or be interpreted as a comprehensive inventory of all job responsibilities required of employees assigned to this job. Employees may be required to perform other duties as assigned.</div><b><br>
Job Requirements</b><div><br>
Required:</div><ul><li>
Bachelors in HTM, Computer Science, Technology, Business disciple upon hire, or equivalent professional experience required</li><li>
Minimum of 5-6 Years in Clinical Engineering Networking Role or equivalent experience.</li><li>
Experience with HIPAA/HITECH compliance standards.
</li><li>Valid Drivers License</li></ul><div></div><div><br>
Preferred:</div><ul><li>
Experience working with the software development life cycle or project management methodologies in addition to Customer Service related experience.</li></ul><div>
This position requires participation in a rotational on-call schedule, including nights, weekends, and holidays. Candidates must be available to respond to urgent service needs outside of regular business hours and may be required to return to the facility on short notice.</div><b>
Where You'll Work</b><div><br>
Inspired by faith. Driven by innovation. Powered by humankindness. CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation&rsquo;s largest nonprofit Catholic healthcare organizations, CommonSpirit Health delivers more than 20 million patient encounters annually through more than 2,300 clinics, care sites and 137 hospital-based locations, in addition to its home-based services and virtual care offerings. CommonSpirit has more than 157,000 employees, 45,000 nurses and 25,000 physicians and advanced practice providers across 24 states and contributes more than $4.2 billion annually in charity care, community benefits and unreimbursed government programs. Together with our patients, physicians, partners, and communities, we are creating a more just, equitable, and innovative healthcare delivery system.</div><b><br>
Pay Range</b><br>
$49.78 - $74.05 /hour</div>

Clinical Engineering Medical Device Security Engineer II

<div><b>Job Summary and Responsibilities</b><div><br>
The Clinical Engineering Med Device Security Eng I mitigates medical device vulnerabilities and threats at a system level by developing and testing remediation instructions, and partnering with cross-functional teams to implement mitigation strategies. In the event of a security incident, this position leads remediation efforts and coordinates with cross-functional teams to return medical devices to service and to implement measures that will prevent future attacks.</div><div></div><div><br>
The Clinical Engineering Med Device Security Eng I has system level responsibilities to safeguard CommonSpirit's medical device environment to ensure device integrity and resilience by assessing, monitoring and responding to security vulnerabilities and threats. This role ensures that medical devices comply with relevant cybersecurity regulations, standards and guidelines.</div><div></div><div><br>
Essential Function</div><ul><li>
Collaborate with cross-functional teams to implement mitigation strategies that address medical device security vulnerabilities and threats.</li><li>
Develop and test medical device security patching and remediation instructions to mitigate risks while also maintaining the integrity of the devices to ensure device reliability and patient safety.</li><li>
In the event of a security incident, lead system wide remediation efforts by coordinating with cross-functional teams to return the devices to service and to implement measures that will prevent future attacks.</li><li>
Conduct comprehensive assessments of system wide medical devices to identify potential security risks and vulnerabilities by reviewing MDS2 forms, and obtaining information from medical device OEMs.</li><li>
Ensure that medical devices comply with relevant cybersecurity regulations, standards and guidelines.</li><li>
Resolve technical challenges and provide support to field technicians.</li></ul><div>
The job summary and responsibilities listed above are designed to indicate the general nature of the work performed within this job. They are not designed to contain or be interpreted as a comprehensive inventory of all job responsibilities required of employees assigned to this job. Employees may be required to perform other duties as assigned.</div><div></div><b><br>
Job Requirements</b><div><br>
Required:</div><ul><li>
Bachelors Other HTM, Computer Science, Technology, Business disciple upon hire or equivalent professional experience required</li><li>
2-4 years experience working in healthcare/IT Security, System Administration, Software Development or related field.</li><li>
1-2 years experience working in a healthcare/medical environment</li><li>
Experience working with specialized medical equipment in a healthcare setting.</li><li>
Experience with Cybersecurity and Infrastructure Security Agency (CISA), HIPAA/HITECH compliance standards.</li><li>
Valid Drivers License</li></ul><div>
Preferred:</div><ul><li>
Experience working with the software development life cycle or project management methodologies.</li></ul><div>
This position requires participation in a rotational on-call schedule, including nights, weekends, and holidays. Candidates must be available to respond to urgent service needs outside of regular business hours and may be required to return to the facility on short notice.</div><div><br>
</div><b>Where You'll Work</b><div><br>
Inspired by faith. Driven by innovation. Powered by humankindness. CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation&rsquo;s largest nonprofit Catholic healthcare organizations, CommonSpirit Health delivers more than 20 million patient encounters annually through more than 2,300 clinics, care sites and 137 hospital-based locations, in addition to its home-based services and virtual care offerings. CommonSpirit has more than 157,000 employees, 45,000 nurses and 25,000 physicians and advanced practice providers across 24 states and contributes more than $4.2 billion annually in charity care, community benefits and unreimbursed government programs. Together with our patients, physicians, partners, and communities, we are creating a more just, equitable, and innovative healthcare delivery system.</div><b><br>
Pay Range</b><br>
$45.26 - $67.32 /hour</div>

Clinical Engineering Medical Device Security Engineer

Blackrock Neurotech

<div><p><b>Job Title:</b> Principal Systems Engineer</p><p><b>
Company: </b>Adraxe</p><p><b>
Job Type:</b> Full-Time</p><p><b>
Location:</b> Plymouth, MN (Hybrid)</p><h1 class="jobSectionHeader"><b>
Adraxe - Company Overview</b></h1><p>
Adraxe Corporation is an innovative medical device startup focused on the design, development, and launch of breakthrough, minimally invasive neuromodulation solutions to address unmet patient needs. The results from the first clinical epilepsy patients are encouraging and we are at the important stage of hiring key personnel, to accelerate our progress and starting our full product and clinical development. Our goal is to revolutionize neurological care with life-compatible, closed-loop neuromodulation therapies, starting with epilepsy.</p><p></p><p><b><br>
About the role</b><br>
We are seeking a highly experienced and technically driven Principal Systems Engineer to lead systems engineering for a closed-loop epilepsy therapy system, with primary emphasis on neural interface performance, end-to-end system integration, full-stack data flow, and optimization of seizure detection algorithms within a regulated (PMA) development framework. The system includes an active implantable medical device (AIMD), custom external instruments, clinician and patient applications, and a secure cloud platform.</p><p><br>
The ideal candidate is a systems engineer who is strongest at the intersection of neural signals + real world data + integrated system behavior who can reason from electrode physics to algorithm metrics to telemetry and cloud pipelines, and knows how to turn that into testable requirements and credible verification evidence. The ideal candidate;</p><ul><li>
Has owned or heavily influenced signal chain and algorithm performance in embedded, constrained systems and is comfortable building evaluation frameworks and test plans that reflect reality, not ideal lab conditions.</li><li>
Understands that &ldquo;algorithm performance&rdquo; isn&rsquo;t just a model score&mdash;it&rsquo;s latency, robustness, power, reliability, data quality, and user workflow.</li><li>
Can lead cross-functional teams through integration complexity with discipline appropriate for PMA.</li></ul><p><br>
This position will report directly to the VP of Engineering, will have significant input into Adraxe strategy and planning, and will collaborate closely with all technical disciplines at Adraxe.</p><p></p><p><b><br>
What you'll do</b><br>
<b>Systems Architecture and Technical Leadership</b></p><ul><li>
Define and maintain the system architecture spanning implant, external instruments, clinician/patient applications, and cloud services.</li><li>
Lead trade studies (power, latency, telemetry, sensing/stimulation performance, reliability, safety, cybersecurity) and drive decisions with cross-functional alignment.</li><li>
Establish and manage interfaces (electrical, RF/telemetry, APIs, data models, workflow integrations) and ensure compatibility across subsystems.</li><li>
Guide development of closed-loop control concepts (sensing  detection/classification  therapy delivery  adaptation), including system-level performance metrics and constraints.</li></ul><p><b>
Neural Interface &amp; Signal Chain Ownership</b></p><ul><li>
Develop deep system-level understanding of the neural interface (electrode-tissue interface, sensing modalities, impedance behavior, artifact sources, saturation, noise, drift) and how it impacts detection and therapy performance.</li><li>
Define and manage requirements for the signal chain (front-end analog, ADC, filtering, sampling, dynamic range, stimulation artifact handling, telemetry constraints) and ensure traceability to detection performance and safety.</li><li>
Partner with hardware, firmware, and clinical teams to characterize signal quality across populations and conditions (movement, sleep, medication changes, electrode maturation).</li></ul><p><b>
Seizure Detection Algorithm Performance &amp; Optimization</b></p><ul><li>
Translate clinical needs into measurable algorithm performance metrics (e.g., sensitivity, false alarm rate, latency to detection, time-in-warning, robustness to artifacts) and establish acceptance criteria.</li><li>
Drive system-level optimization across algorithm + firmware + data pipeline to meet performance targets under real device constraints (compute, memory, power, latency).</li><li>
Lead closed-loop performance analyses that connect sensing  detection  therapy behavior, including edge cases and failure modes.</li><li>
Coordinate creation of curated datasets, labeling strategies, ground-truth definitions, and evaluation protocols (including subgroup and scenario performance).</li></ul><p><b>
End-to-End Data Flow &amp; Observability (Implant </b><b> External </b><b> Apps </b><b> Cloud)</b></p><ul><li>
Define and validate the complete system data flow: on-device data generation, event markers, compression/packetization, telemetry, external device handling, app storage/display, cloud ingestion, processing, and analytics.</li><li>
Ensure data integrity across the lifecycle: time synchronization, identity mapping, provenance, audit trails, retention, and traceability required for regulated evidence.</li><li>
Specify and validate observability features: logging, metrics, error reporting, trace IDs, and tools to support troubleshooting, clinical workflows, and post-market surveillance.</li></ul><p><b>
System Integration &amp; Test Leadership (PMA-Grade Evidence)</b></p><ul><li>
Own the integrated system test strategy with emphasis on realistic, high-value integration coverage (HIL/SIL, simulated physiology, induced artifacts, telemetry stress, app/cloud failure modes).</li><li>
Define system-level test methods and rigs to validate sensing and detection performance under representative conditions (including stimulation artifact conditions if applicable).</li><li>
Drive integration readiness criteria, defect triage workflows, and release gating for end-to-end functionality.</li><li>
Ensure traceability from user needs and hazards to verification evidence across the integrated system.</li></ul><p><b>
Safety, Risk, and Performance Boundaries for Closed-Loop Operation</b></p><ul><li>
Lead identification of hazards and risk controls related to detection performance, therapy timing, and data integrity (e.g., missed detection, false positives, telemetry dropouts, timebase drift, data corruption).</li><li>
Define safe bounds and fallback behaviors (therapy limits, safe modes, detection confidence gating, watchdogs) and verify they work across system states and failures.</li></ul><p><b>
Verification, Validation, and Test Strategy</b></p><ul><li>
Lead design verification testing (DVT) and verification planning to ensure compliance with medical device standards and safety requirements.</li><li>
Ensure designs meet relevant standards (e.g., IEC 60601, ISO 14708, ISO 14971, EMI/EMC compliance).</li><li>
Define end-to-end system verification and validation strategy across implant + external + applications + cloud, including integration and system testing.</li><li>
Develop test environments (benchtop rigs, simulators, HIL/SIL as appropriate, clinical workflow simulations)</li><li>
Data-driven verification of sensing/detection/therapy performance (as applicable)</li><li>
Drive design reviews, ensure readiness for formal V&amp;V, and support PMA documentation and inspection readiness.</li></ul><p><b>
Cross-Functional Leadership and Mentorship</b></p><ul><li>
Lead technical alignment across firmware, hardware, algorithms, app engineering, cloud, clinical, quality, regulatory, and manufacturing.</li><li>
Mentor systems engineers and establish best practices for systems engineering rigor, documentation quality, and integration readiness.</li><li>
Communicate clearly with stakeholders, translating complex technical tradeoffs into decision-ready options and documented outcomes.</li></ul><p><b>
Qualifications</b><br>
<b>Minimum Qualifications are:</b></p><ul><li>
B.S. in Systems, Computer Science, Electrical Engineering, Biomedical Engineering, Mechanical Engineering, or related field.</li><li>
10+ years (or equivalent) experience in systems engineering for complex electromechanical and software-intensive products; medical device experience strongly preferred.</li><li>
Demonstrated experience developing implantable and/or active therapeutic devices (e.g., neuromodulation, cardiac rhythm management, or similar).</li><li>
Experience with implantable sensing modalities and neural signals (e.g., iEEG/ECoG/SEEG or related), including artifact sources and long-term recording challenges.</li></ul><p><b>
Strong command of:</b></p><ul><li>
Requirements development, decomposition, and traceability</li><li>
System architecture and interface definition (ICDs)</li><li>
System integration and V&amp;V planning and execution for distributed systems</li><li>
Risk management and safety engineering in regulated contexts</li><li>
Proven ability to lead through influence across multi-disciplinary teams and drive cross-functional execution.</li><li>
Strong written and verbal communication skills, including the ability to produce clear, inspection-ready technical documentation.</li></ul><p></p><p><b><br>
Preferred Qualifications</b></p><ul><li>
M.S. or Ph.D. in Electrical Engineering, Biomedical Engineering, or related field.</li><li>
Experience supporting PMA development (design controls, DHF evidence, traceability, and system V&amp;V evidence packages).</li><li>
Experience with seizure detection/classification and/or robust biosignal detection methods in real-world settings.</li><li>
Experience designing and validating end-to-end data pipelines for regulated products (time sync, provenance, auditability, retention, access control).</li><li>
Strong background in system integration testing for distributed systems (embedded + apps + cloud), including SIL/HIL, simulation, and test automation.</li><li>
Working knowledge of cybersecurity engineering for connected medical systems (threat modeling, encryption, key management, vulnerability management).</li></ul><p></p><p><b><br>
Physical and Other Requirements</b></p><ul><li>
This position is located in Plymouth MN.</li><li>
This position is a hybrid position with an expectation of roughly 75% in office and 25% remote work.</li><li>
This position requires approximately 15% Travel including international travel.</li></ul></div><p></p>

Adraxe: Principal Systems Engineer

Amazon.com

<div><h2 class="jobSectionHeader"><b>DESCRIPTION</b></h2><div>
Amazon LEO is an initiative to launch a constellation of Low Earth Orbit satellites that will provide low-latency, high-speed broadband connectivity to unserved and underserved communities around the world.
<br>
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MSE is responsible for delivering software that runs on custom hardware, and helps manage satellite manufacturing. We are looking for an engineer with experience in device software, tcp communications, system level c/c++/rust programming experience along with knowledge of foundational AWS cloud services such as IAM, Lambdas, Step functions, Cloud watch etc.<br>
<br>
The candidate would participate in all phases of software development from requirements through implementation and test to operations. You will engage with an experienced cross-disciplinary staff to conceive and design solutions. You must be responsive, flexible, and able to succeed within an open, collaborative peer environment. You will work with cross-functional partner teams and lead efforts with engineers from requirements to deployment.
<br>
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You will participate in the design, integration and improvement of the SW. This includes designing and implementing a wide range of low-level software on our hardware and other low level programming activities.
<br>
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Export Control Requirement:<br>
Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum.<br>
<br>
Key job responsibilities<br>
<ul><li>Design and Implement System Architecture for Manufacturing Dev Test Lab</li><li>Partner with device software, frontend, networking, and security engineering teams to build scalable lab infrastructure</li><li>Scale production implementation to support global deployments to manufacturing and CM sites</li></ul><br>
A day in the life<br>
This role is for a Software Development Engineer who will design and build launch support equipment and support LEO manufacturing operations. You will be building low-latency, highly scalable architecture that are critical to getting high quality internet service to customers.</div><h2 class="jobSectionHeader"><b><br>
BASIC QUALIFICATIONS</b></h2><ul><li>3+ years of non-internship professional software development experience</li><li>2+ years of non-internship design or architecture (design patterns, reliability and scaling) of new and existing systems experience</li><li>Experience programming with at least one software programming language</li></ul><h2 class="jobSectionHeader"><b>
PREFERRED QUALIFICATIONS</b></h2><ul><li>3+ years of full software development life cycle, including coding standards, code reviews, source control management, build processes, testing, and operations experience</li><li>Bachelor's degree in computer science or equivalent</li></ul><br>
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.<br>
<br>
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you&rsquo;re applying in isn&rsquo;t listed, please contact your Recruiting Partner.<p><br>
The base salary range for this position is listed below. Your Amazon package will include sign-on payments and restricted stock units (RSUs). Final compensation will be determined based on factors including experience, qualifications, and location. Amazon also offers comprehensive benefits including health insurance (medical, dental, vision, prescription, Basic Life &amp; AD&amp;D insurance and option for Supplemental life plans, EAP, Mental Health Support, Medical Advice Line, Flexible Spending Accounts, Adoption and Surrogacy Reimbursement coverage), 401(k) matching, paid time off, and parental leave. Learn more about our benefits at https://amazon.jobs/en/benefits.</p><br>
USA, WA, BELLEVUE - 143,700.00 - 194,400.00 USD annually</div><p></p>

Software Engineer - MSE, Manufacturing Systems Engineering

Dynaflex Technologies

<p>Compensation</p><ul><li>Base Salary: $54,000 annually (post-probation)</li><li>Ramp Period (First 3 Months): structured training with reduced base (~$40,800 annualized)</li><li>Additional Compensation: Commission, Performance Bonus, Benefits (medical, dental, vision, PTO</li></ul><p>This is a full-time, entry-level Sales Engineer role designed for individuals seeking a long-term career in med-tech. The first 3 months are a high-intensity probation period focused on performance, learning speed, and ownership. You will contribute to real customer work from day one. Evaluation based on technical learning speed, communication, work ethic, and ownership. Top performers transition into long-term roles</p><p>What We&rsquo;re Looking For</p><ul><li>Relentless follow-through</li><li>Technical curiosity</li><li>Commercial instinct</li><li>Coachability under pressure</li></ul><p>Basic Qualifications</p><ul><li>Bachelor&rsquo;s degree or equivalent experience</li><li>0&ndash;2 years experience (sales, engineering, or technical environment)</li></ul><p>Dynaflex is a medical device component manufacturer looking for responsible and hardworking individuals to join our growing team. We aim to make a difference in this world by making quality and innovative medical catheters/extrusion to improve patient outcomes. This is a family owned business and all our employees treat each other with care and respect. We believe that employees are part of a family instead of just numbers. Lots of opportunities to grow as we are a multinational operation with facilities in Northern California, Southern California, and Taiwan.</p><p>We specialize in the areas including Neurovascular Coil Delivery, Heart Valve Repair and Replacement Catheter System, Steerable EP Catheters and Sheaths, Balloon and Self Expanding Stent Delivery Systems.</p><p>We are looking for a motivated and well-spoken Sales Engineer to join our team. The Sales Engineer will be responsible for developing new leads, communicating with customers, understanding their needs, and ensuring a smooth sales process.</p><p>To be successful as Sales Engineer, you should be able to build instant rapport and achieve customer satisfaction. Knowledge of medical devices, research and analytical skills, and the ability to explain clearly are highly desired skills.</p><p><b>Sales Engineer Responsibilities:</b></p><ul><li>Serve customers by identifying their needs and engineering adaptations of products, equipment, and services.</li><li>Identify current and future customer service requirements by establishing personal rapport with potential and actual customers and others in a position to understand service requirements.</li><li>Provide product, service, or equipment technical and engineering information by answering questions and requests.</li><li>Establish new accounts by identifying potential customers and planning and organizing sales call schedules.</li><li>Prepare cost estimates by studying all related customer documents, consulting with engineers and other professional personnel.</li><li>Determine improvements by analyzing cost-benefit ratios of equipment, supplies, or service applications in customer environment and engineering or proposing changes in equipment, processes, or use of materials or services.</li><li>Gain customer acceptance by explaining or demonstrating cost reductions and operations improvements.</li><li>Prepares sales engineering reports by collecting, analyzing, and summarizing sales information and engineering and application trends.</li><li>Contribute to sales engineering effectiveness by identifying short-term and long-range issues that must be addressed, recommend options and courses of action, and implementing directives.</li><li>Contribute to team effort by accomplishing related results as needed.</li></ul><p><b>Sales Engineer Qualifications / Skills:</b></p><ul><li>Problem solving</li><li>Product knowledge</li><li>Selling to customer needs</li><li>Software requirements</li><li>Product development</li><li>Presentation skills</li><li>Technical understanding</li><li>Verbal communication</li><li>Requirements analysis</li><li>Innovation</li></ul><p><b>Sales Engineer Requirements:</b></p><ul><li>Bachelor&rsquo;s degree in Engineering preferred (Biomedical, Industrial, Mechanical, or Electrical), or equivalent industry experience</li><li>Previous experience in an outbound call center or a related sales position preferred.</li><li>Proficiency in Microsoft Office</li><li>Ability to read and understand documents</li><li>Ability to communicate needs and follow up</li><li>Attention to detail</li><li>Ability to work with sensitive material</li><li>Seeking someone who is driven, communicates well, has a good hardworking attitude.</li></ul><p>Job Type: Full-time</p><p>Pay: From $54,000.00 per year</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li></ul><p>People with a criminal record are encouraged to apply</p><p>Work Location: In person</p>

Sales Engineer (Medical Devices)

Hydrafacial

<div><p><b>About Us</b></p><p>
Hydrafacial is a global category-creating company focused on bringing innovative products to market and delivering beauty health experiences by reinventing our consumer&rsquo;s relationship with their skin, their bodies and their self-confidence.</p><p></p><p>
Every person here is a key player in our success. We are firm believers in making the little things count each day so the big things will follow. If this sounds like you, come check us out! This is the perfect opportunity to work with some of the best leaders in the industry while you gain the global and strategic experience to add to your professional toolbox.</p><p><b><br>
Job Description:</b></p><p></p><div><div><p><b>
The Role:</b></p></div><p></p><div><p>
The R&amp;D Engineer will support the research and development engineering of Hydrafacial's innovative medical aesthetic devices. This role is ideal for an early-career engineer who is passionate about product development in a regulated environment and eager to contribute to a category-defining brand. You will collaborate cross-functionally with R&amp;D, Quality, Regulatory, and Operations teams to bring next-generation skin health technologies to market.</p></div><p></p><div><p><b>
What</b><b> </b><b>you&rsquo;ll</b><b> </b><b>do:</b></p></div><div><p>
Primary Responsibilities:</p></div><div><ul><li><p>
Support the design and development of electro-mechanical assemblies for new and sustaining aesthetic device platforms.</p></li><li><p>
Assist in the creation and maintenance of design control documentation in accordance with FDA 21 CFR 820.30, including Design History Files (DHFs), Design Input/Output documents, Verification &amp; Validation protocols, and reports.</p></li><li><p>
Contribute to the generation and review of engineering requirements, test protocols, technical reports, and risk management documentation (FMEA, hazard analysis).</p></li><li><p>
Assist in the preparation and execution of design verification and validation (V&amp;V) testing.</p></li><li><p>
Create and revise engineering drawings and CAD models; support tolerance stack-up and design-for-manufacturability reviews.</p></li><li><p>
Utilize 3D printing and rapid prototyping tools to support concept development and design iterations.</p></li><li><p>
Collaborate with cross-functional teams to support Change Orders (COs), Engineering Change Requests (ECRs), and deviations.</p></li><li><p>
Support sustaining engineering activities including failure investigations, root cause analysis, and corrective actions (CAPAs).</p></li><li><p>
Maintain organized and compliant documentation in accordance with ISO 13485 Quality Management System requirements.</p></li><li><p>
Other duties as assigned.</p></li></ul></div><p></p><div><p><b>
What you need to know:</b></p></div><div><p>
Experience/Skills/Education:</p></div><div><p>
Required:</p></div></div><div><div><ul><li><p>
B.S. degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, or a related technical field</p></li><li><p>
0&ndash;3 years of experience in a product development or engineering role (internship, co-op, or full-time experience accepted)</p></li><li><p>
Familiarity with electro-mechanical assembly design and integration</p></li><li><p>
Basic understanding of FDA design controls (21 CFR 820.30) and/or ISO 13485 quality management systems</p></li><li><p>
Proficiency or coursework experience with CAD software (SolidWorks preferred)</p></li><li><p>
Strong attention to detail and ability to maintain accurate, compliant documentation</p></li><li><p>
Effective written and verbal communication skills with the ability to work in a collaborative, cross-functional environment</p></li></ul></div><p></p><div><p>
Desired:</p></div><div><ul><li><p>
Experience with or exposure to FDA-regulated medical device development</p></li><li><p>
Knowledge of aesthetic or consumer wellness devices</p></li><li><p>
Hands-on experience with 3D printing / rapid prototyping technologies</p></li><li><p>
Familiarity with ISO 13485 QMS implementation</p></li><li><p>
Understanding of GD&amp;T and engineering drawing standards</p></li><li><p>
Experience with design verification/validation (V&amp;V) testing</p></li></ul><p></p><p><b>
We mean it when we say you&rsquo;ll LOVE this role.</b></p><p>
Base Pay: $30.00-$35.00/hour</p><p></p><p>
An employee&rsquo;s pay position within the salary range will be based on several factors, including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, travel requirements, revenue-based metrics, any contractual agreements, and business or organizational needs. The range listed is just one component of Hydrafacial's total rewards package for our employees. Other rewards may include annual bonuses, long-term incentives based on level, paid time off, and region-specific benefits. Come grow and GLOW with us!</p><p></p><p><b>
What else can you expect with Hydrafacial?</b><br>
PERKS! Benefits include: Medical insurance, dental insurance, vision insurance, FSAs, HSAs, accident insurance, pet insurance, company-paid life and AD&amp;D insurance, company-paid long-term and short-term disability insurance, 401(k) with employer match, paid time off (PTO), and paid holidays.</p><p></p><p>
#LI-Onsite</p></div></div><p></p><p>
Hydrafacial is proud to be an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, sex, religion, sexual orientation, national origin, gender identity, gender expression, age, disability, genetic information, pregnancy or any other protected characteristic as outlined by color, federal, state or local laws. We are committed to working with and providing accommodation to applicants with physical and mental disabilities.</p><p><br>
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Associate R&D Engineer - Long Beach, CA

House Conditioner

<p><b>Job Title:</b> Smart Home Systems Engineer</p><p><b>Company:</b> House Conditioner<br/><b>Location:</b> Al Waab Street, Building 45, Al Rayyan, Doha, Qatar<br/><b>Salary:</b> QAR 27,000 per month</p><p>Job Overview</p><p>House Conditioner is seeking a skilled and innovative <b>Smart Home Systems Engineer</b> to support the design, implementation, and optimization of intelligent residential technology systems. This role is ideal for a professional with expertise in automation systems, smart technologies, systems integration, and technical problem-solving.</p><p>The Smart Home Systems Engineer will be responsible for supporting connected systems, improving performance, and delivering technology solutions that enhance efficiency, functionality, and user experience.</p><p>Key Responsibilities</p><ul><li>Design, configure, and support smart home systems and integrated automation solutions.</li><li>Manage installation, testing, troubleshooting, and optimization of connected technologies.</li><li>Support systems related to automation, controls, networking, and intelligent device integration.</li><li>Analyze system performance and recommend improvements or upgrades.</li><li>Prepare technical documentation, system reports, and engineering recommendations.</li><li>Collaborate with internal teams and clients to support project requirements and implementation.</li><li>Ensure systems meet quality, safety, and operational standards.</li><li>Support maintenance planning and technical issue resolution.</li><li>Contribute to innovation and process improvements in smart systems engineering.</li></ul><p>Qualifications</p><ul><li>Bachelor&rsquo;s degree in Engineering, Information Technology, Electronics, or related field.</li><li>Proven experience in systems engineering, automation, smart technologies, or related roles.</li><li>Strong knowledge of integrated systems, networking, and automation technologies.</li><li>Excellent troubleshooting, analytical, and problem-solving skills.</li><li>Strong communication and project coordination abilities.</li><li>Ability to manage technical priorities in a dynamic environment.</li><li>Relevant certifications are a plus.</li></ul><p>What We Offer</p><ul><li>Competitive salary of <b>QAR 27,000 per month</b></li><li>Professional growth opportunities</li><li>Innovative and collaborative work environment</li><li>Opportunity to contribute to advanced smart technology projects</li></ul><p><b>House Conditioner is an equal opportunity employer.</b></p><p>الراتب المدفوع: QAR٢٧٬٠٠٠٫٠٠&nbsp;لكل شهر</p><p>موقع العمل: بشكل شخصي</p>

Smart Home Systems Engineer

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