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<h3>Job Description</h3>
Job DescriptionSalary: 
About us
Arwood Machine, AVulcanFormsCompany, is a well-established ISO-9001:2015, AS9100D, ISO 13485 certified, ITAR compliant high precision machining, automation, and assembly business in Newburyport, Massachusetts. We are a digital production facilityleveragingautomated precision machining for defense, aerospace, medical, and other critical industries. In operation since 1965, Arwood has been committed to quality and excellence for over five decades.
Arwood Machine, aVulcanFormsCompany,seeks a Staff Customer Quality Engineerfor our Newburyport, MA location.
 
Job Purpose
We are seeking a dedicated and proactive Staff Customer Quality Engineer to join our team. In this role, you will manage, create, and drive the execution of customer complaints while interfacing directly with customers to implement their requirements onto the plant floor. You will work closely with cross-functional teams to identify root causes and implement effective solutions.
 Key Responsibilities Oversee the management of customer complaints, ensuring timely resolution and effective communication with stakeholders. Interface directly with customers to understand and implement their quality requirements on the plant floor. Create and implement processes for tracking and analyzing customer feedback and quality issues. Conduct Root Cause and Corrective Action (RCCA) investigations and complete Supplier Corrective Action Requests (SCARs) as required by customers. Collaborate with engineering, manufacturing, and customer service teams to identify and resolve quality concerns. Develop and maintain quality documentation, including reports and process maps. Drive continuous improvement initiatives based on customer feedback and quality metrics. Conduct training sessions on quality standards and processes for team members.
 Qualifications Bachelors Degree or 3-5+ years equivalent experience in a medical device or aerospace environment 3+ years of experience in a quality job role 2+ years of experience in a customer complaint analysis or investigative role 1+ years of experience gathering data and performing a Root Cause Corrective Action Experience in an aerospace, medical device, or manufacturing environment
 Preferred Qualifications Experience in Quality Management Systems (QMS) within a Supplier Quality organization Experience interfacing and presenting to senior and executive leadership Experience reading and interpreting engineering drawings and specifications Experience working closely with other engineering disciplines in an integrated team environment Experience with regulatory requirements Experience reviewing contracts, managing suppliers, and/or experience working with inventory Preferred auditing accreditation to ASD9100 or ISO13485.

Staff Customer Quality Engineer

<h3>Job Description</h3>
Job DescriptionAbout Us
We are a global team of like-minded Med-Tech professionals focused on patient centric solutions in a collaborative environment leading to excellent outcomes. We have developed an advanced and unique heart failure therapy technology in the BrioVAD® Left Ventricular Assist System (LVAS). We are introducing the BrioVAD LVAS to Heart Failure clinicians for use with the large number of indicated and untreated patients who could benefit from chronic mechanical circulatory support. The initiation of our INNOVATE™ Trial in the US is only the beginning. We are building a team to develop advanced technology intended to further improve patient outcomes, increase therapy acceptance, and enable chronic MCS therapy to be accessible to more patients across the globe.
 
Job Summary
BrioHealth Solutions is seeking a dedicated and experienced Senior Quality Engineer to support the development, implementation, and ongoing maintenance of our Quality Management System (QMS). This role is pivotal in ensuring compliance with FDA QMSR, ISO 13485, EU MDR, and other regulatory standards critical to our medical device operations. The ideal candidate will be responsible for managing internal audits, organizing management review meetings, and tracking essential quality documentation for product registrations and regulatory submissions. In addition, you will collaborate cross-functionally to drive continuous improvement efforts and ensure the quality of our heart failure therapies meets the highest standards. This is an onsite position located in Burlington, MA, with up to 15% travel required.
 
Responsibilities
Quality Management System (QMS)
<ul>
<li>Support the development, implementation, and maintenance of the company's Quality Management System (QMS) to ensure compliance with FDA QMSR, ISO 13485, EU MDR, and other applicable regulations and standards.</li>
<li>Organize and conduct internal audits to evaluate the effectiveness of the QMS and ensure adherence to regulatory requirements.</li>
<li>Aid in the organization of management review meetings and is responsible for tracking action items, ensuring timely closure, and follow-up on the review outputs.</li>
<li>Assist in the preparation and management of essential quality system documents for product registrations, including domestic and FDA submissions.</li>
<li>Play a key role in managing relevant medical device quality regulations, including the evaluation, update, training, and implementation of related quality system documents.</li>
<li>Assist in coordinating external audits, including system certification inspections, to ensure compliance with quality standards.</li>
<li>Contribute to the development, tracking, and monitoring of key performance indicators (KPIs) related to quality, ensuring continuous improvement.</li>
<li>Collect and analyze data from quality management workflows and provides detailed reports to the Quality Assurance (QA) team, functional leaders, and senior management.</li>
<li>Deliver training and ongoing support to ensure employees understand and adhere to quality system processes.</li>
</ul>
Cross Functional Collaboration
<ul>
<li>Lead cross-functional teams with persistence and determination, driving the integration of new process technologies aimed at improving quality management workflows and product quality.</li>
<li>Work closely with departments such as R&amp;D, manufacturing, supply chain, and regulatory affairs to ensure alignment with quality objectives and address department-specific needs.</li>
</ul>
Additional Responsibilities
<ul>
<li>Conduct quality assurance audits and assessments to verify compliance with established quality management system requirements.</li>
<li>Perform statistical analysis on quality data to identify trends and areas for improvement and drive the implementation of corrective and preventive actions (CAPAs).</li>
<li>Supports regulatory inspections and audits, addressing non-conformities and ensuring the implementation of corrective actions.</li>
<li>Stay current with evolving regulations, guidelines, and industry best practices related to medical device design, development, and quality assurance.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Engineering, Science, or a related field.</li>
<li>At least 5 years of hands-on experience in Quality Management Systems (QMS) within the medical device industry, specifically with Class III sterile medical devices.</li>
</ul>
 Nice to Have
<ul>
<li>Master's degree or higher in Engineering, Science, or a related field.</li>
<li>Experience in quality management systems, with a focus on Class III active implantable and life-supporting medical devices.</li>
<li>Strong expertise in design control processes, risk management principles, and quality management systems.</li>
<li>In-depth understanding of relevant regulatory requirements and industry standards, including FDA QSR/QMSR, ISO 13485, EU MDR, and ISO 14971.</li>
<li>Results-driven with a strong focus on aligning quality initiatives with business priorities.</li>
<li>Proven ability to lead and influence cross-functional teams in a highly matrixed organization to achieve quality and business objectives.</li>
<li>Proficient in utilizing statistical methods and tools for data analysis and driving quality improvement initiatives.</li>
<li>Excellent verbal and written communication skills, with the ability to effectively present to senior leadership and engage teams. </li>
<li>Strong interpersonal skills for building collaborative relationships across all levels.</li>
<li>Certifications
<ul>
<li>ASQ Certified Quality Engineer (CQE).</li>
<li>DMAIC Lean / Six Sigma Certification, with demonstrated success in leading DMAIC projects to drive continuous improvement. </li>
</ul>
</li>
</ul>

Senior Quality Engineer - Quality Management System (QMS)

<h3>Job Description</h3>
Job DescriptionSalary: 
About us
Arwood Machine, A VulcanForms Company, is a well-established ISO-9001:2015, AS9100D, ISO 13485 certified, ITAR compliant high precision machining, automation, and assembly business in Newburyport, Massachusetts. We are a digital production facility leveraging automated precision machining for defense, aerospace, medical, and other critical industries. In operation since 1965, Arwood has been committed to quality and excellence for over five decades.
Arwood Machine, A VulcanForms Company, seeks a Staff Quality Engineer for our Newburyport, MA location.
Job Purpose
As a Staff Quality Engineer at Arwood Machine, A VulcanForms Company, you will be a hands-on engineer in a role involving machining and manufacturing complex parts and products. VulcanForms Inc. is a manufacturer of complex, high value engineered components in serial production at the world's most powerful additive foundry.
Key Accountabilities
<ul>
<li>Develops and drives measurable Quality improvements relating to products and processes</li>
<li>Ensure Inspecting and Testing of materials, equipment, processes, and products to meet quality specifications.</li>
<li>Create test and inspection method and develop and execute test method validations</li>
<li>Collaborate to develop and implement quality and process controls and improvements.</li>
<li>Assure the QMS conforms to the customer, internal, industry (i.e., AS9100, ISO 9001, ISO 13485), and regulatory/legal requirements.</li>
<li>Engage and support shop floor personnel and manufacturing defect prevention teams to ensure alignment on top priorities (using baseline data and future forecast). These tools are used to drive and facilitate compliance resolution, containment, Root Cause Analysis and Corrective Action Implementation within closed loop process controls.</li>
<li>Perform process walks, operator observations, and lead manufacturing team discussions to drive process enhancements to reduce variation.</li>
<li>Lead/Drive Advanced Product Quality Planning (APQP) initiatives (PFMEA, control Plans, SPC, etc.) using baseline metrics and future demand with the ability to perform verification/validation of improvements and efficiencies to facilitate defect prevention.</li>
<li>Integrate product and process verifications such as First Articles and audits throughout value stream processes to prevent quality escapes, optimize throughput and assure on-time delivery of products and services.</li>
</ul>
Qualifications
<ul>
<li>Knowledge of Root Cause Analysis, Data analysis, and Statistical Process Control concepts</li>
<li>Experience in first article inspection reports (FAIRs), quality monitoring, and leading root cause correct actions for both short-term and long-term initiatives in a cross functional environment.</li>
<li>Experience in manufacturing process knowledge with Quality systems and industry technical standards (ISO 9001, AS9100 and/or AS9102), interpreting drawings, work instructions, Bill of Materials (BOMs), consumable materials control, process disciplines and tool control.</li>
<li>Experience with Advanced Product Quality Planning (APQP)/AS9145; Utilizing tools such as PPAP, Key Characteristics, DFMEA, PFMEA and/or Control Plans</li>
<li>Expertise in Geometric Dimension and Tolerancing blueprint interpretations</li>
</ul>
Benefits
<ul>
<li>Medical, dental, vision, and life insurance are available to you starting on your first day of employment</li>
<li>Generous time off package, including vacation PTO, sick PTO, and 14 company-paid federal holidays</li>
<li>401(k) with company match and stock option</li>
</ul>
VulcanForms Inc. is committed to being an Equal Opportunity Employer, valuing employees with diverse, multi-cultural perspectives. We are dedicated to fostering an inclusive environment, empowering our team, and embracing diversity. We welcome all applicants and ensure fair and impartial treatment regardless of race, color, religion, sex, national origin, ancestry, citizenship status, age, legally protected physical or mental disability, protected veteran status, status in the U.S. uniformed services, sexual orientation, gender identity or expression, marital status, genetic information, or any other characteristic protected by applicable federal, state, or local law.

Staff Quality Engineer

<h3>Job Description</h3>
Job Description
CAD Drafter (High-End Stone Fabrication)
Location: Everett, MA | Work Type: In-Person | Pay: $20$30/hour
Join a Legacy of Excellence in Custom Stonework
Take the next step in your drafting career with a company known for precision, craftsmanship, and artistry.
Are you a detail-oriented drafter who thrives in a fast-paced, custom fabrication environment? Are you energized by collaborating with engineers, project managers, and shop teams to bring one-of-a-kind installations to life?
This is a rare opportunity to join a seasoned team at Cumar one of the nation's premier sources for custom stone design where your drawings dont just live on a screen, but become luxury kitchens, bathrooms, fireplaces, and commercial masterpieces.
If you're looking to deepen your technical skills in a collaborative, growth-minded shop, this role could be the perfect fit.
Why This Opportunity?
<ul>
<li>Reputation &amp; Legacy Over 30 years in business and known for premium quality in the New England design community.</li>
<li>Work That Inspires Contribute to high-end, custom residential and commercial stone projects each one unique.</li>
<li>Tight-Knit Team Work alongside five other drafters and collaborate daily with shop, field, and engineering teams.</li>
<li>Benefits &amp; Schedule Full-time (MF, 85), 40-hour week with some flexibility. PTO, sick time, health/dental/vision, and 401k after 6 months.</li>
<li>Competitive Pay $20$30/hour, depending on experience.</li>
</ul>
What Youll Be Doing
<ul>
<li>Draft clean, accurate 2D AutoCAD drawings based on wooden templates, site scans, and sketches.</li>
<li>Prepare detailed shop ticket packages for CNC and fabrication teams.</li>
<li>Collaborate with engineers and project managers to resolve technical questions quickly.</li>
<li>Visit the shop floor regularly to ensure drawings translate clearly to fabrication.</li>
<li>Occasionally visit local job sites to verify templates and field details.</li>
<li>Create annotated photo layouts and organize scanner data for templating workflows.</li>
<li>Offer process improvements and ideas that drive accuracy and efficiency.</li>
</ul>
What You Bring
<ul>
<li>AutoCAD Expertise 45 years of drafting experience in a fabrication or construction-related setting.</li>
<li>Industry Familiarity Able to read blueprints and architectural drawings with ease.</li>
<li>Measurement Proficiency Comfortable with tape measures and photo documentation tools.</li>
<li>Strong Communication Can navigate conversations across engineering, shop, and field teams.</li>
<li>Initiative Proactive problem solver who checks and double-checks before issues arise.</li>
<li>Comfort in a Shop Setting While you wont be machining, familiarity with shop workflows is key.</li>
</ul>
Are you ready to join a team that values precision, design, and craftsmanship and where your work becomes something beautiful? Apply today and lets talk about where your CAD skills can take you next.
Who is Bronwick?
Bronwick helps professionals like you find the best jobs in the stone industry. We handle hiring for over 100 shops around the nation. We know this industry and we know the path to advancing your career. We're here to make the hiring process easier. Apply now to get started!

CAD Drafter

<h3>Job Description</h3>
Job Description
Lantheus is headquartered in Bedford, Massachusetts with offices in Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio.
Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone’s health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team.
This position site-based and requires a presence on-site 5 days per week.
Position Summary:
We are seeking an experienced and driven Process Engineer II to support commercial and clinical manufacturing of ultrasound enhancing agents and radiopharmaceutical drug products. This position plays a critical role in ensuring robust, compliant, and efficient production processes for sterile injectable and device-combination products. The ideal candidate brings 6+ years of hands-on experience in cGMP manufacturing support, with a strong understanding of sterile drug production, radiopharmaceutical workflows, and medical device quality systems.
Key Responsibilities:
· Provide day-to-day technical support to manufacturing operations, ensuring reliable production.
· Lead investigations for moderate- to high-complexity deviations, perform root cause analyses, and implement CAPAs in collaboration with QA and operations teams.
· Author and revise controlled documents, including manufacturing documentation, technical reports, protocols (e.g., process validation, equipment qualification), and risk assessments.
· Support process monitoring, trending, and data analysis activities to drive continuous improvement and maintain a state of control.
· Participate in cross-functional teams for process changes, equipment upgrades, and lifecycle projects, ensuring alignment with regulatory and quality requirements.
· Act as a technical contributor in change control execution, including impact assessments, protocol generation, and implementation planning.
· Support and/or lead multiple technical transfers, scale-ups, and process validation activities.
· Collaborate with stakeholders in Manufacturing, QA, QC, Engineering, and Supply Chain to ensure timely and compliant execution of manufacturing campaigns.
· Ensure compliance with applicable regulations, including 21 CFR Parts 210, 211, 820, EU GMP Annex 1, and radiation safety requirements.
· Support readiness activities for internal and regulatory audits, including documentation review and SME participation.
Qualifications:
· Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Nuclear Engineering, Chemistry, or a related technical field (advanced degree preferred).
· 6+ years of experience in pharmaceutical manufacturing, with a strong focus on sterile injectable or radiopharmaceutical production.
· Solid understanding of cGMPs, aseptic processing, cleanroom operations, and medical device/combination product regulations (21 CFR 210, 21 CFR 211, 21 CFR 820, ISO 13485).
· Demonstrated ability to investigate deviations, problem solve, and execute changes within a quality system framework. Advanced technical writing skills required.
· Hands-on experience with equipment commonly used in sterile fill/finish operations.
· Familiarity with process validation, equipment qualification, and risk management principles.
· Self-starter with strong interpersonal and communication skills; able to work independently and in cross-functional teams.
· Proficiency in Excel, data analysis tools, and electronic document/change control systems (e.g., TrackWise, CATSWeb). Skilled at presenting technical content to technical and non-technical audiences.
Preferred Experience:
· Experience in handling radioactive materials or supporting radiopharmaceutical manufacturing environments.
· Knowledge of lean manufacturing principles and process improvement methodologies.
· Experience in lifecycle management of commercially approved pharmaceutical products and devices.
· Experience in managing large cross-functional projects in a matrix environment.
Work Environment &amp; Physical Requirements:
· Work in cleanroom environments and radiation-controlled areas required.
· Some off-shift or weekend coverage may be needed based on production schedules.
Core Values
The ideal candidate will embody Lantheus core values:
· Let people be their best
· Respect one another and act as one
· Learn, adapt, and win
· Know someone’s health is in our hands
· Own the solution and make it happen
Lantheus is an equal opportunity employer that provides a workplace free from discrimination. All qualified applicants and employees are considered without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any other characteristic protected by law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at <a href="mailto:talentacquisition@lantheus.com" target="_blank">talentacquisition@lantheus.com</a>.

Process Engineer II

<h3>Job Description</h3>
Job DescriptionPOSITION SUMMARY We’re seeking a proactive and detail-oriented Quality Engineer to ensure that our product development processes meet quality, regulatory and company standards. You will play a pivotal role in design quality and development lifecycle, supporting cross-functional teams, and helping to shape our robust Quality Management System (QMS) to meet our business requirements. Key Responsibilities
<ul>
<li>Serve as the design quality engineer taking development projects from concept through commercialization.&nbsp;</li>
<li>Ensure compliance with applicable standards and regulations, including ISO 13485, FDA 21 CFR Part 820, and EU MDR.</li>
<li>Lead and support design control activities: risk management (ISO 14971), design inputs/outputs, verification and validation, design reviews, and design history file (DHF) maintenance.</li>
<li>Develop and implement quality plans, test strategies, and protocols for new product development.</li>
<li>Drive root cause analysis and corrective/preventive actions (CAPA) related to product design and development.&nbsp;</li>
<li>Monitor and analyze quality metrics and trends. Support development and continuous improvement of the Quality Management System.</li>
<li>Participate in technical design reviews and project phase reviews.&nbsp;</li>
<li>Review and approve Engineering Change Orders (ECOs), test protocols, and technical documentation.</li>
<li>Collaborate with Product Management, Engineering, R&amp;D, Regulatory, Manufacturing, Customer Success and Clinical teams to ensure quality is integrated throughout the product lifecycle.</li>
<li>Support internal, external audits and regulatory inspections.</li>
<li>Provide Quality representation during problem resolution supporting a risk-based approach for processes.&nbsp;</li>
<li>Establish and maintain metrics and reports for design quality performance.</li>
</ul>
Key Skills/Abilities
<ul>
<li>Strong knowledge of FDA QSR, ISO 13485, ISO 14971, and EU MDR.</li>
<li>Demonstrated ability to interpret engineering drawings, specifications, and technical documents.</li>
<li>Strong verbal and written communication skills, ability to present issues, plans, and objectives</li>
<li>Strong documentation, analytical, and organizational skills</li>
<li>Skilled in risk management techniques, root cause analysis, and statistical tools.</li>
<li>Excellent communication and organizational skills with the ability to work independently and cross-functionally.</li>
<li>Certified Quality Engineer (CQE) or other relevant certifications such as Six Sigma preferred.</li>
</ul>
Education/Experience
<ul>
<li>Bachelor’s degree in Engineering, Biomedical Engineering, or related technical discipline.</li>
<li>Minimum 5 years of experience in Quality Engineering within the medical device industry.</li>
<li>Experience working in a smaller, more agile environment is a strong plus.</li>
<li>Experience working with contract manufacturers and suppliers.</li>
<li>Experience with tools such as FMEA, CAPA, Root Cause Analysis (5 Whys, Fishbone), and control charts.</li>
<li>Experience with software as a medical device (SaMD) or digital health technologies preferred.&nbsp;</li>
</ul>
Location: Waltham, MA 02451, 4-5 days onsite required Employment Type: Full-Time Reports To: Director of Quality and Regulatory We offer competitive salary and benefits! 401(k) plans &amp; matching, Health, Dental &amp; Vision Insurance, Short &amp; Long Term Disability, Parental Leave, Life Insurance, Stock Options, EAP &amp; voluntary benefits. ABOUT CONVERGENT DENTAL: Convergent Dental, Inc. is a privately owned dental equipment and technology company. Our high-energy, high-tech culture is experiencing rapid growth and looking for new team members who can grow with us. Our flagship product, Solea®, is the only CO2 laser to be cleared by the FDA for all-tissue indications and delivers an anesthesia-free, blood-free, suture-free experience. Solea® is a true breakthrough in dental laser technology that offers a completely different experience for both dentists and patients when compared to traditional instruments or any earlier laser treatment. Solea’s speed and precision is a result of its wavelength and computer controls that are unique to Convergent Dental, Inc. We are a high-energy team, and looking for new&nbsp; members who can grow with us. Our culture is fast paced, collaborative, and a roll up your sleeves entrepreneurial environment. We are all working towards forever changing how people think about going to the dentist. If you are a motivated, career-oriented individual, Convergent Dental is the place for you! Convergent Dental is committed to developing a diverse and talented team. All candidates are encouraged to apply.&nbsp; If you are excited about this role but are unsure whether you meet 100% of the requirements, we encourage you to inquire and/or apply.

Quality Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Quality ControlPay: Flexible (based on experience) Location: Gardner Shift: 3rdRequirements: Must have transportation

Quality Control

<h3>Job Description</h3>
Job Description
The STR Sensors Division is at the forefront of developing advanced signal processing algorithms and prototyping systems for next-generation radar and electronic warfare technologies. We focus on defense, intelligence, and homeland security sectors and our known for our ability to address complex national security challenges.
STR takes pride in creating a culture of innovation and collaboration. We collaborate with a dynamic group of research engineers across STR, academic researchers, and industry partners to develop practical and effective solutions to RF sensing and counter-sensing challenges. Together, we're dedicated to tackling some of the toughest problems faced by our national security-focused clients.
If you're seeking an opportunity to apply your deep technical knowledge and creativity to make a lasting impact in national security, we invite you to join us. 
The Role:
As a Lead Systems and RF Research Scientist, you will help drive the system design, integration and test, and demonstration of sensing and counter sensing systems for radar, electronic warfare and other applications. You will work closely with the signal processing team to identify and prioritize objective capabilities. You will collaborate across the company to leverage lessons learned, tools, etc. to ensure that STR remains at the forefront of current and emerging needs.
What you will do:
<ul>
<li>Collaborate with the team to quantify goals, system performance objectives, performance metrics, dependencies, and risks to guide program execution</li>
<li>Lead and work with multi-disciplinary teams to architect, implement, and test RF hardware systems enabling novel sensing, electronic warfare, and signal processing systems</li>
<li>Perform trade studies and analyses of proposed hardware architectures. Systems predominantly field deployable prototypes with the objective of transitioning to low-volume product systems</li>
<li>Design, calibrate, and implement and perform bench-top unit tests. Document results including correlation with objective system performance</li>
<li>Work with signal processing team on innovative sensing system test concepts and execution methods. Develop supporting system analytical test tools/measures</li>
<li>Design, document, and implement over-the-air system demonstrations, identifying hardware readiness, test architecture, performance metrics, data management, operational procedures, and performance reports</li>
<li>Review system effectiveness and identify opportunities to advance and/or mature subsystems and system capabilities</li>
<li>Document system design and performance for customer review. Present results to customers</li>
<li>Support business development and proposal writing efforts for next-generation RF hardware system development opportunities</li>
</ul>
Who you are:
<ul>
<li>This position requires the ability to obtain a security clearance, for which U.S. citizenship is required by U.S. Government </li>
<li>BS in Electrical Engineering, Applied Mathematics, Physics, or a related technical discipline</li>
<li>Demonstrated team leadership and mentoring.</li>
<li>8+ years' experience working with hardware system design. Expertise with RF components and subsystems, including T/R modules, rotary joints, pedestal, filters, radiating structures, isolators, amplifiers, ADC/DAC, etc.</li>
<li>Design experience in:
<ul>
<li>RF systems, subsystem and/or component analysis (frequency planning, link budget analysis, transceiver architectures, cascade analysis)</li>
<li>Electromagnetics &amp; RF/wave propagation</li>
</ul>
</li>
<li>Skilled in RF component/subsystem/system test and measurement equipment and techniques (anechoic chambers, oscilloscopes, vector network analyzers, spectrum analyzers, signal generators)</li>
<li>Proficiency in MATLAB and/or Python and/or other higher-level languages</li>
<li>Strong Mathematical, troubleshooting, written, and verbal communication skills</li>
</ul>
Even Better:
<ul>
<li>Active Secret or TS/SCI Clearance</li>
<li>Advanced degree in Electrical Engineering, Applied Mathematics, Physics, or a related technical discipline </li>
<li>Experience with:
<ul>
<li>RF systems engineering and technologies in one or more of the following areas: sensing and electronic warfare applications including electronic attack, electronic protection, cognitive EW, radar, and advanced ESM techniques</li>
<li>EM Field Solvers (ANSYS HFSS, Sonnet)</li>
<li>Interacting with decision-makers and customers to translate mission needs into an end-to-end analytical solution</li>
</ul>
</li>
<li>Prior design experiences in:
<ul>
<li>Antennas</li>
<li>RF Printed Circuit Boards</li>
<li>RF Integrated Circuits</li>
<li>RF Transceiver building blocks (power amplifiers, low-noise amplifiers, oscillators, mixers, filters)</li>
</ul>
</li>
<li>Knowledge of:
<ul>
<li>Mechanical design</li>
<li>Designing and debugging for EMI/EMC requirements</li>
<li>FPGA hardware inference designs</li>
</ul>
</li>
<li>Background in designing for manufacturability, producibility, and cost constraints</li>
<li>Ability to apply novel, innovative and interdisciplinary approaches to challenging engineering problems </li>
<li>Ability to create and present briefings to customers and senior management to provide both high-level and deep technical solution explanations</li>
</ul>
STR is a growing technology company with locations near Boston, MA, Arlington, VA, near Dayton, OH, Melbourne, FL, and Carlsbad, CA. We specialize in advanced research and development for defense, intelligence, and national security in: cyber; next generation sensors, radar, sonar, communications, and electronic warfare; and artificial intelligence algorithms and analytics to make sense of the complexity that is exploding around us.
STR is committed to creating a collaborative learning environment that supports deep technical understanding and recognizes the contributions and achievements of all team members. Our work is challenging, and we go home at night knowing that we pushed the envelope of technology and made the world safer.
STR is not just any company. Our people, culture, and attitude along with their unique set of skills, experiences, and perspectives put us on a trajectory to change the world. We can't do it alone, though - we need fellow trailblazers. If you are one, join our team and help to keep our society safe! Visit us at <a href="http://www.str.us" target="_blank">www.str.us</a> for more info.
 STR is an equal opportunity employer. We are fully dedicated to hiring the most qualified candidate regardless of race, color, religion, sex (including gender identity, sexual orientation and pregnancy), marital status, national origin, age, veteran status, disability, genetic information or any other characteristic protected by federal, state or local laws.
If you need a reasonable accommodation for any portion of the employment process, email us at <a href="mailto:appassist@str.us" target="_blank">appassist@str.us</a> and provide your contact info.
Pursuant to applicable federal law and regulations, positions at STR require employees to obtain national security clearances and satisfy the requirements for compliance with export control and other applicable laws.

Lead Systems and RF Research Scientist

<h3>Job Description</h3>
Job DescriptionBenefits/Perks
<ul>
<li>Competitive Compensation</li>
<li>Great Work Environment</li>
<li>Career Advancement Opportunities</li>
</ul>
Job SummaryWe are seeking a Quality Assurance Engineer to join our team! As a Quality Assurance Engineer on the team, you will be working closely with many different teams and departments to support new product development, determine the best production processes, and improve current production processes to streamline efficiency. You will also train new operators and technicians on best practices, conduct internal and external audits with the company and suppliers, and troubleshoot problems as they arise. The ideal candidate has excellent analytical skills, is comfortable working independently or within a team, and has strong attention to detail.&nbsp; Responsibilities&nbsp;
<ul>
<li>Work with different departments to develop new products and processes</li>
<li>Examine current manufacturing processes to see where improvements could be made</li>
<li>Train and mentor new and existing employees on best manufacturing practices</li>
<li>Troubleshoot problems with staff and suppliers</li>
<li>Conduct audits internally and with suppliers to maintain high standards</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s in Engineering or equivalent field</li>
<li>Previous experience working in quality control desired</li>
<li>Strong communication and organizational skills</li>
<li>Excellent attention to detail</li>
<li>Strong analytical skills</li>
</ul>

<h3>Job Description</h3>
Job Description
Job Summary:
Emerald Technologies is seeking a quality-focused professional to lead cross-functional efforts in ensuring product excellence throughout the lifecycle. This role involves driving root cause analysis, corrective actions, and continuous improvement initiatives.
Key Responsibilities:
<ul>
<li>Collaborate across departments to reduce defects and customer complaints.</li>
<li>Lead and document corrective actions using structed problem-solving (e.g., 8D, 5-Why, Fishbone).</li>
<li>Investigate and resolve nonconforming materials and support MRB activities.</li>
<li>Respond quickly to production floor issues to minimize downtime.</li>
<li>Support new product introductions and ensure readiness for production.</li>
<li>Train and clarify staff in IPC standards (IPC-A-610, IPC-J-STD-001, including Space Addendum).</li>
<li>Assist in developing clear, effective work instructions aligned with IPC requirements.</li>
<li>Communicate with customers and suppliers to resolve quality concerns and drive improvements.</li>
<li>Maintain SOPs and records related to quality processes, training, and corrective actions.</li>
<li>Analyze defect trends to identify and implement proactive quality improvements.</li>
<li>Participate in material disposition and purge activities as needed.</li>
<li>Perform other duties as assigned. </li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in electrical engineering or a comparable degree within manufacturing or engineering. (Preferred) </li>
<li>5–7 years of experience in a quality or engineering role in manufacturing.</li>
<li>CIT in IPC-A-610 and/or IPC-J-STD-001. (Preferred)</li>
<li>Knowledge of statistical methods.</li>
<li>Knowledge of root cause analysis and problem-solving methodologies.</li>
<li>Demonstrated ability to use Microsoft Windows and Microsoft Office Programs.</li>
<li>Capable of performance in high-demand situations.</li>
<li>Demonstrated fair, and ethical behaviors.</li>
<li>Demonstrated interpersonal and communication skills. </li>
</ul>
Physical Demands and Work Environment:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
<ul>
<li>While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to sit. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; stoop, kneel, or crouch. The employee must be able to lift and/or move up to 25 pounds. Specific vision abilities perception and ability to adjust focus. </li>
<li>This position operates in an office environment. This role routinely uses standard office equipment such as computers, photocopiers, etc. </li>
</ul>

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