Vendor quality supervisor jobs near me

Only applications submitted through **************************** will be reviewed. Altech Services, Inc. (ALTECH), is a diversified national service organization providing field services for the railroad, commuter rail, and IT industries since 1990. Our mission is to provide timely and quality support services that contribute to client and employee growth. ALTECH stands behind its service with a strong dedication to customer satisfaction, industry expertise, and quality assurance. Job Description On-call, working from home location, travel to vendors' operations for vendor surveillance. States of coverage: North Carolina, South Carolina, and Georgia. Must be available for travel at short notice. This role is to work directly with the vendors to support: corrective action/non-conformance management-vendor; FAI (first article inspection) Responsibilities First Article Inspections Work directly w/vendors to support: corrective action/non-conformance management FAI (first article inspection); issue and manage RSA (Request for Supplier Action) Participate in Engineering and Quality investigations Product Quality and Conformity; QIR (Quality Investigation Request)-vendor. Source inspection; create and monitor KPI for assigned vendors Qualifications Requirements and Skills Familiar w/Engineering methods, work and material planning in relation to Quality activities Possess working knowledge of computer applications including word processing and databases Able to work in a team environment and must possess team facilitation skills. Good organizational skills/the ability to set/prioritize tasks/ability to work independently Must possess a valid passport and driver's license Education 4 year degree/certificate in Quality, Aeronautical, Mechanical, Industrial/Manufacturing Engineering Additional Information To apply, please visit ****************************

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: SecretTRAVEL: Yes, 75% of the TimeDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Mission Systems (NGMS) is currently seeking a Principal Supplier Quality Engineer to join our Sector team in Maryland. This is a remote position mainly working with suppliers in mainly in Maryland and other states mainly within Eastern Seaboard, with up to 75% travel. What you will do: Responsible for managing supplier quality risks. Develop and implement systems for evaluating and controlling supplier quality. Ensure supplier processes and products meet contractual, regulatory, and technical requirements. Interfaces directly with supplier personnel to assess quality and manufacturing processes. Conducts product and process verification, monitors supplier quality performance, and leads root cause analysis and corrective actions for supplier quality issues. Manages supplier requests for waivers, deviations, and oversees the discrepancy reporting process. Keeps management informed of supplier performance, quality status, and associated risks. Coordinates and oversees the implementation of Supplier Quality plans throughout all program phases. Actively participates in supplier evaluation, qualification, and selection during the Business Acquisition Process and for new procurements on existing programs. Manages the implementation of Supplier Quality processes, including supplier approval, source selection, supplier classification (Critical, Key, Standard), development and execution of supplier quality risk assessments and mitigation plans, and flow-down of supplier quality requirements. Basic Qualifications BS degree in STEM related field with a minimum of 5 years of relevant engineering and/or manufacturing experience; MS Degree with a minimum of 3 years of relevant experience in engineering and/or manufacturing. Experience with conducting product/ process validation in accordance with AS9102 (First Article Inspection) or similar process in other industries. Experience with Evaluation and Implementation of quality management systems such as ISO9001/AS9100 or equivalent. Experience with Root Cause analysis using tool such as but not limited to 5-Whys, Fishbone (Ishikawa) Diagram. Experience working with mechanical design requirements and specifications. US citizenship Ability to obtain DoD Security Clearance. Requires extensive travel (75-95%), often on short notice. Preferred Qualifications: Degree in Mechanical, Electrical, or related Engineering. Experience with APQP and PPAP processes. Familiarity with various manufacturing processes, including machining, forging, heat treating, welding, and brazing. Experience with Root Cause analysis and problem-solving techniques like FMEA and SIPOC. Experience leading process improvement projects. Experience in leading audits, New Product Introduction (NPI) and Production Readiness Reviews. Primary Level Salary Range: $91,200.00 - $136,800.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Who We Are PathAI is on a mission to improve patient outcomes with AI-powered pathology. We are transforming traditional pathology methods into powerful, new technologies. These innovations in pathology can help accelerate drug development, improve confidence in the accuracy of diagnosis, and get life-saving therapies to patients more quickly. At PathAI, you'll work with a diverse and talented team of people, who are dedicated to solving complex problems and making a huge impact. Where You Fit As the Senior Regulatory and Quality Specialist, you will be a key member of PathAI's Regulatory and Quality (RAQA) Team, ensuring compliance to the company's Quality Management System and to pre- and post-market regulations that pertain to PathAI's RUO, IVD, and clinical products. You will be responsible for representing RAQA in company-specific projects for diagnostic and clinical development services and will be involved in process improvement efforts, participate in audits as needed, and may be responsible for maintaining/managing key QMS processes (e.g., document control). You will provide risk and regulatory assessments during design control and change control activities and participate in the development and submission of filings to regulatory agencies in the US, EMA, and other geographies. The ideal candidate brings knowledge in regulatory affairs and quality assurance, preferably in the context of AI-driven diagnostic software, and thrives in a fast-paced, high-growth environment. What You'll Do Regulatory strategy, submissions, reviews Build and execute global regulatory plans; prepare and coordinate pre-subs, 510(k)s, de novos, PMAs, and ex-US filings; participate in agency interactions. Shape registration strategy and author the technical file/design dossier content in partnership with Product, ML, Clinical, and Engineering. May review and approve product promotional material and customer notifications to ensure alignment with regulatory status. Quality system Maintain and improve QMS processes aligned to FDA QSR/21 CFR 820, ISO 13485, ISO 14971, IEC 62304, and related standards; monitor new/updated regulations and flow them into the QMS. Participate as subject matter expert in customer audits, certification body audits and regulatory inspections as needed. Design controls &SaMD lifecycle Guide teams through design inputs/outputs, V&V, risk management, usability, design transfer, and clinical/labeling impacts; review design documentation for compliance throughout the product life cycle. Cross-functional enablement Serve as the day-to-day RAQA partner to Product/ML/Engineering/Clinical/LabOps, resolving issues that affect project timelines. What You Bring Experience: 5+ years of progressive experience in regulatory affairs and quality assurance in IVD medical devices, preferably SaMD with AI/ML Demonstrated participation in regulatory submissions for FDA Class II/III devices and some ex-US regulatory experience (e.g., EMA IVDR Class A-C); experience with CDx submissions is a plus Working knowledge of global regulatory standards, including FDA QSR, ISO 13485, IVDR, and ISO 14971. Experience authoring and reviewing QMS documentation (e.g., procedures, protocols, reports) Educational Background: Bachelor's degree in engineering, physical, or life sciences (advanced degree preferred) Skills & Competencies: Strong organizational skills with the ability to manage multiple projects in a dynamic environment. Ability to manage details effectively while contributing to broader regulatory strategies. Strong interpersonal and communication skills, with the ability to collaborate effectively with cross-functional teams. Demonstrated success working within and maintaining FDA/ISO compliant Quality Systems We Want To Hear From You At PathAI, we are looking for individuals who are team players, are willing to do the work no matter how big or small it may be, and who are passionate about everything they do. If this sounds like you, even if you may not match the job description to a tee, we encourage you to apply. You could be exactly what we're looking for. PathAI is an equal opportunity employer, dedicated to creating a workplace that is free of harassment and discrimination. We base our employment decisions on business needs, job requirements, and qualifications - that's all. We do not discriminate based on race, gender, religion, health, personal beliefs, age, family or parental status, or any other status. We don't tolerate any kind of discrimination or bias, and we are looking for teammates who feel the same way. The cash compensation outlined below includes base salary or hourly wage and on-target commission for employees in eligible roles. The summary below indicates if an employee in this position is eligible for annual bonus, overtime pay and equity awards. Individual compensation packages are tailored based on skills, experience, qualifications, and other job-related factors. Annual Pay Range: $101,250 - $155,250 Not Overtime Eligible Eligible for Equity #LI-Remote

The Senior Specialist, Quality Program Management and Performance implements new and existing healthcare quality improvement activities to maintain compliance with quality program requirements and reporting and monitoring for key quality program activities. Acts as a lead specialist to provide project, program, and/or initiative related direction. Provides guidance for other specialists within the department and/or collaboratively with other departments to ensure quality programs meet regulatory requirements. Job Duties Acts as a lead specialist to provide project-, program-, and/or initiative-related direction and guidance for other specialists within the department and/or collaboratively with other departments to ensure quality programs meet regulatory requirements Implements key quality program activities that maintain quality compliance, including maintaining responsibility for preparing and finalizing quality program management committee and other meeting documentation, which capture thorough discussion and participation of attendees, follow-up actions, and next steps, in a clear and understandable way Oversees quality program management activities, which include preparation for quality improvement audits, surveys, and other federal and state-required quality activities Monitors and ensures that key quality activities are completed on time and accurately to present results to key departmental management and other Molina departments, and to formal committees and subcommittees as needed Writes narrative reports and works with departmental specialists (as appropriate) to interpret regulatory specifications, explain programs and results of programs, and document findings Maintains quality program management project plan to ensure state (and/or federal and NCQA-related) requirements are documented during the year Works with the Manager and/or Director to maintain up-to-date addendums to quality policies and procedures that clearly document state-specific activities and requirements in collaboration with the national teams Creates, manages, and/or compiles the required documentation to maintain critical quality improvement functions Leads quality improvement activities, meetings, and discussions with and between other departments within the organization Evaluates project/program activities and results to identify opportunities for improvement Surfaces to the Manager and/or Director any gaps in processes that may require remediation Other tasks, duties, projects, and programs assigned This position may require same-day out-of-office travel 0 - 50% of the time, depending upon the location This position may require multiple days' out of town overnight travel 0 - 20% of the time, depending upon location Job Qualifications REQUIRED QUALIFICATIONS: Bachelor's Degree or equivalent combination of education and work experience Min. 3 years of experience in healthcare with a minimum of 2 years of experience in health plan quality improvement, managed care, or equivalent experience Demonstrated solid business writing experience Operational knowledge and experience with Excel and Visio (flow chart equivalent) PREFERRED QUALIFICATIONS: Degree in Preferred field: Clinical Quality, Public Health, or Healthcare 5 years of experience in health plan quality management Experience with data reporting, analysis, and/or interpretation Active, unrestricted Certified Professional in Health Quality (CPHQ) Active, unrestricted Nursing License (RN may be preferred for specific roles) Active, unrestricted Certified HEDIS Compliance Auditor (CHCA) To all current Molina employees: If you are interested in applying for this position, please apply through the intranet job listing Molina Healthcare offers a competitive benefits and compensation package Molina Healthcare is an Equal Opportunity Employer (EOE) M/F/D/V

Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The person in this position is responsible for conducting quality control (QC) review of clinical and regulatory documents, reports, data tables, and slide presentations in support of drug development as well as assisting with the oversight of QC projects assigned to contractors and CROs. In addition, this person is responsible for supporting medical writing activities with supervision. Essential Job Functions and Responsibilities: These may include but are not limited to: Perform comprehensive QC reviews of clinical and regulatory documents, reports, data tables, and slide presentations in accordance with predefined, ambitious timelines. Edit documents for grammar, punctuation, consistency, and adherence to internal style guides and regulatory requirements. Collaborate with medical writers, regulatory affairs, and cross-functional teams to resolve discrepancies and ensure document quality. Organize complex QC projects and provide guidance to other QC reviewers. Support authoring process for plain language documents, including but not limited to informed consent forms and plain language protocol synopses. Assist in maintaining and updating Crinetics Style Guide. Support medical writing activities with supervision as needed. Ability to work in a dynamic environment and manage changing priorities across multiple projects. Complete other tasks as assigned. Education and Experience: Required: Bachelor's or Master's degree in a scientific discipline required; advanced life sciences degree preferred. A minimum of 5 years' experience conducting QC data reviews and editing. Experience with regulatory documents for the biotech/pharmaceutical industry preferred (equivalent combination of experience and education considered). Expert attention to detail. Highly organized and methodical work style. Familiarity with electronic document control and management systems. Experience working on regulatory submissions (IND, NDA, MAA, NDS, etc) in eCTD format preferred. Excellent standard of written English, and ability to communicate fluently and effectively in written and spoken English. Preferred: Ability to manage multiple projects and adapt to changing priorities for successful project completion. Task-oriented view of work with a commitment to timelines and deliverables. Excellent proficiency in MS Word with experience adhering to templates and style guides; proficient with other MS Office Suite applications, including Excel and PowerPoint. Experience in authoring plain language documents. Team-oriented with excellent communication and interpersonal skills; demonstrated ability in managing indirectly. Strong time management skills. Physical Demands and Work Environment: Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities. Laboratory Activities (if applicable): Biology and chemical laboratory environment experience needed. Environmental health and safety requirements also apply. Travel: You may be required to travel for up to 5% of your time. The Anticipated Base Salary Range: In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience and education. Crinetics Pharmaceuticals is a multi-state employer, and this salary range may not reflect positions that work in other states. Your recruiter can share more about the specific salary range during the hiring process. Equal Opportunity Employer: Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender (including gender identity and/or expression), pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws. Salary Range The salary range for this position is: $90000 - $115000. In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

Who we are Samsara (NYSE: IOT) is the pioneer of the Connected Operations™ Cloud, which is a platform that enables organizations that depend on physical operations to harness Internet of Things (IoT) data to develop actionable insights and improve their operations. At Samsara, we are helping improve the safety, efficiency and sustainability of the physical operations that power our global economy. Representing more than 40% of global GDP, these industries are the infrastructure of our planet, including agriculture, construction, field services, transportation, and manufacturing - and we are excited to help digitally transform their operations at scale. Working at Samsara means you'll help define the future of physical operations and be on a team that's shaping an exciting array of product solutions, including Video-Based Safety, Vehicle Telematics, Apps and Driver Workflows, and Equipment Monitoring. As part of a recently public company, you'll have the autonomy and support to make an impact as we build for the long term. About the role: Samsara's Quality Automation and Engineering (QAE) team uses test engineering, automation, and data analysis skills to drive product quality so that our customers can realize the full benefits of our platform. To further the goal of quality, we are seeking to invest in automation, strengthen our frameworks, and integrate with hardware and software. We're looking for an experienced automation engineer to increase our automation coverage for Vehicle Gateway or Safety products within the VG firmware product group. This is a remote role open to candidates residing in the US. You should apply if: You want to impact the industries that run our world: The software, firmware, and hardware you build will result in real-world impact-helping to keep the lights on, get food into grocery stores, and most importantly, ensure workers return home safely. You want to build for scale: With over 2.3 million IoT devices deployed to our global customers, you will work on a range of new and mature technologies driving scalable innovation for customers across industries driving the world's physical operations. You are a life-long learner: We have ambitious goals. Every Samsarian has a growth mindset as we work with a wide range of technologies, challenges, and customers that push us to learn on the go. You believe customers are more than a number: Samsara engineers enjoy a rare closeness to the end user and you will have the opportunity to participate in customer interviews, collaborate with customer success and product managers, and use metrics to ensure our work is translating into better customer outcomes. You are a team player: Working on our Samsara Engineering teams requires a mix of independent effort and collaboration. Motivated by our mission, we're all racing toward our connected operations vision, and we intend to win-together. In this role, you will: Champion automation frameworks and collaborate with engineering teams to design APIs that prioritize automation from the start, within a close-knit Firmware Quality. Partner with your QE Lead/Manager, Engineering, and Automation framework teams to define quality goals, expand test coverage, and focus on an automation-first strategy. Focus on automation of new features & existing regression test cases to minimize regression cycle time & improve overall quality of product. Build & execute automation tests simulating real-world scenarios to find defects & regressions, triage with relevant stakeholders, and publish detailed dashboards/reports. Develop an automation strategy to facilitate testing activities throughout Samsara product life cycles. Integrate hardware infrastructure for simulation, hardware validation, and product development. Champion, role model, and embed Samsara's cultural principles (Focus on Customer Success, Build for the Long Term, Adopt a Growth Mindset, Be Inclusive, Win as a Team) as we scale globally and across new offices. Minimum requirements for the role: Bachelor's degree or higher, preferably in Electrical or Computer Engineering. At least five years of experience in developing automated test frameworks and software tools for product development and validation. Strong understanding of test system architectures and understands build, release test pipeline within SDLC. Understanding of embedded or distributed systems. Experience in setting up automated test environments and building test beds with physical hardware. Demonstrated proficiency in debugging, troubleshooting, and root cause analysis. Excellent communication skills, with the ability to collaborate effectively across teams with diverse backgrounds. An ideal candidate also has: Built or worked on customer shipping software. Familiarity with testing devices that use wireless protocols such as BLE, WiFi, LTE, and GNSS. Proven experience in defining test plans, triaging test failures, and reporting results and relevant metrics. Has worked on designing and developing hardware infrastructure for testing applications (e.g., power measurement tools, RF testing, etc.). Has worked with data analysis tools and packages, including SQL, Pandas, Databricks, and others. Hands-on experience with test instrumentation, including power supplies, power analyzers, battery simulators, call boxes, and GPS simulators. Samsara's Compensation Philosophy: Samsara's compensation program is designed to deliver Total Direct Compensation (based on role, level, and geography) that is at or above market. We do this through our base salary + bonus/variable + restricted stock unit awards (RSUs) for eligible roles. For eligible roles, a new hire RSU award may be awarded at the time of hire, and additional RSU refresh grants may be awarded annually. We pay for performance, and top performers in eligible roles may receive above-market equity refresh awards which allow employees to achieve higher market. The range of annual base salary for full-time employees for this position is below. Please note that base pay offered may vary depending on factors including your city of residence, job-related knowledge, skills, and experience.$126,140-$212,000 USD At Samsara, we welcome everyone regardless of their background. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, age, and other characteristics protected by law. We depend on the unique approaches of our team members to help us solve complex problems and want to ensure that Samsara is a place where people from all backgrounds can make an impact. Benefits Full time employees receive a competitive total compensation package along with employee-led remote and flexible working, health benefits, and much, much more. Take a look at our Benefits site to learn more. Accommodations Samsara is an inclusive work environment, and we are committed to ensuring equal opportunity in employment for qualified persons with disabilities. Please email ********************************** or click here if you require any reasonable accommodations throughout the recruiting process. Flexible Working At Samsara, we embrace a flexible working model that caters to the diverse needs of our teams. Our offices are open for those who prefer to work in-person and we also support remote work where it aligns with our operational requirements. For certain positions, being close to one of our offices or within a specific geographic area is important to facilitate collaboration, access to resources, or alignment with our service regions. In these cases, the job description will clearly indicate any working location requirements. Our goal is to ensure that all members of our team can contribute effectively, whether they are working on-site, in a hybrid model, or fully remotely. All offers of employment are contingent upon an individual's ability to secure and maintain the legal right to work at the company and in the specified work location, if applicable. Fraudulent Employment Offers Samsara is aware of scams involving fake job interviews and offers. Please know we do not charge fees to applicants at any stage of the hiring process. Official communication about your application will only come from emails ending in ‘@samsara.com' or ‘@us-greenhouse-mail.io'. For more information regarding fraudulent employment offers, please visit our blog post here.

Headway's mission is a big one - to build a new mental health care system everyone can access. We've built technology that helps people find great therapists with the first software-enabled national network of providers accepting insurance. 1 in 4 people in the US have a treatable mental health condition, but the majority of providers don't accept insurance, making therapy too expensive for most people. Headway is building a new mental healthcare system that everyone can access by making it easy for therapists to accept insurance and scale their practice. Headway was founded in 2019. Since then, we've grown into a diverse, national network of over 60,000 mental healthcare providers across all 50 states who run their practice on our software and have served over 1 million patients. We're a Series D company with over $325m in funding from a16z (Andreessen Horowitz), Accel, GV (formerly Google Ventures), Spark Capital, Thrive Capital, Forerunner Ventures and Health Care Service Corporation. We want your time here to be the most meaningful experience of your career. Join us, and help change mental healthcare for the better. About The Role At Headway, we're building the future of behavioral health quality and safety. We're hiring a Principal, Prescriber Clinical Quality to spearhead our clinical quality monitoring initiatives and lead our Ongoing Professional Practice Evaluation Program. You'll work cross-functionally with Operations, Compliance, Product, Engineering, and other teams to build robust clinical quality frameworks and optimize chart review workflows. This is an exceptional opportunity to reimagine how behavioral health quality is defined and measured at a rapidly scaling, mission-driven company. You will: Lead Headway's clinical quality strategy, developing protocols and processes that uphold safety, efficiency, and effectiveness standards for the practice. Build and scale our Professional Practice Evaluation programs, directly improving clinical outcomes across our provider network Conduct routine chart reviews and monitoring, providing feedback to clinicians and creating remediation plans for documentation concerns Collaborate with Product teams to ensure our EHR meets industry clinical standards and develop automated quality monitoring systems Supervise clinical teams and peer reviewers, building clinical oversight capabilities as we scale Partner with cross-functional teams to optimize workflows and create scalable feedback systems for providers You will love this role if: You are a Psychiatric Mental-Health Nurse Practitioner (PMHNP) with 8+ years of post-graduate experience in both clinical practice and fast-paced business environments You have extensive experience completing quality chart reviews and audits for healthcare organizations, with a track record of training others on clinical documentation standards You are a thought leader passionate about reimagining behavioral health quality, ideally with experience across traditional healthcare organizations, public health systems, and/or healthcare startups You thrive as a collaborator, building bridges between clinical strategy and product, operations, and business teams You are a strategic first-principles thinker who can decompose complex problems into clear strategies and actionable plans You have experience supervising clinicians or large provider teams, with strong performance management skills You are motivated by the opportunity to improve access to high-quality behavioral healthcare at scale Compensation and Benefits: The expected base pay range for this position is $172,720 - $254,000, based on a variety of factors including qualifications, experience, and geographic location. We are committed to offering a comprehensive and competitive total rewards package, including robust health and wellness benefits, retirement savings, and meaningful ownership opportunities through equity. Compensation decisions are made holistically, ensuring fairness and alignment with market benchmarks while recognizing individual contributions and potential. Benefits offered include: Equity Compensation Medical, Dental, and Vision coverage HSA / FSA 401K Work-from-Home Stipend Therapy Reimbursement 16-week parental leave for eligible employees Carrot Fertility annual reimbursement and membership 13 paid holidays each year as well as a Holiday Break during the week between December 25th and December 31st Flexible PTO Employee Assistance Program (EAP) Training and professional development We believe a team's strength is in its people, and we cannot achieve this mission without a team that reflects the diversity of this problem - across race, ethnicity, gender, sexuality, age, national origin, religion, family status, disability, military status, and experience. Headway is committed to the full inclusion of all qualified individuals. As part of this commitment, Headway will ensure that persons with disabilities are provided with reasonable accommodations. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or receive other benefits and privileges of employment, please inform the recruiter when they contact you to schedule your interview. Headway participates in E-Verify. To learn more, click here.

It's a new day with a new opportunity at 8am! About the role: We are seeking an experienced Senior Quality Engineer to join our Quality Engineering team at 8am. In this role, you will serve as a customer advocate and quality champion for your embedded scrum team, ensuring the functionality, reliability, performance, and user experience of our FinTech/Back-End SaaS platform through comprehensive testing strategies and collaborative engineering practices. At 8am, Quality is not a phase-it's a mindset woven into every conversation, decision, and line of code. As a senior member of the team, you'll leverage your deep testing expertise to drive quality improvements that impact not just your immediate team but the broader engineering organization. You'll mentor junior engineers, contribute to process improvements, and take ownership of quality initiatives that protect and enhance our customers' experience. About us: At 8am, our vision is to power a world where professionals thrive. We start every day on a mission to empower professionals with the most trusted, innovative technology to deliver world-class outcomes for their clients and exceptional financial results for their business. They count on our purpose-built solutions to simplify operations, ensure compliance, and fuel profitable growth, so they can focus on their clients and do more of the work that matters. Founded in 2005, 8am™ (formerly AffiniPay) is the professional business platform built to help legal, accounting, and other client-focused professionals run stronger, more profitable businesses. Today, more than 250,000 professionals across the U.S. trust 8am to help them work smarter, serve clients better, and unlock their full potential. We have been recognized as one of Inc 5000's fastest growing companies in the U.S. for 13 years in a row, and as a result, our teams continue to grow as well! What you'll do: Customer Advocacy & Technical Excellence Champion the customer experience at every stage of development, viewing deliverables through the customer's lens Design and execute comprehensive test strategies across UI, API, and database layers, ensuring they reflect real customer scenarios Speak up when features aren't complete enough to test or when quality concerns arise-even if it means slowing down Challenge requirements that don't serve customer needs and identify issues that could frustrate users before they reach production Write high-quality test cases that tell a story about customer interactions and maintain them through their entire lifecycle Identify and document defects with comprehensive root cause analysis, always including "how this affects the customer" assessments Drive continuous improvement in our Defect Leakage Rate (≤15% target), recognizing that every bug reaching production erodes customer trust Leadership & Execution Complete 90%+ of assigned tasks independently while providing guidance and mentorship to junior engineers Own quality initiatives and drive measurable improvements to QE processes and standards Create and lead test plan reviews using test management tools like TestRail or Qase, ensuring adherence to documented standards Engage with Product Owners and Product Management on feature feasibility, testability, and requirement clarification Become a Subject Matter Expert (SME) for specific technical areas or product components Track and report on Quality KPIs, with particular focus on Defect Leakage Rate-our primary customer-focused metric that measures bugs caught by QE versus those found by customers Collaborate with SDET team/Developers on determining what tests are high value for automation, and ensuring that test automation operates as expected, owning automated test execution. Technical Proficiency Demonstrate proficient to advanced networking and Linux skills, utilizing command-line tools across common distributions Leverage Python scripting for assisting with test automation tasks as necessary (Dedicated SDET team owns framework and most automation tasks). Willingness to learn basic Python scripting if not previously leveraged Validate services deployed on AWS and other cloud platforms, managing test environments and cloud resources efficiently Basic understanding of security and performance testing Collaboration & Communication Work effectively within scrum team, and across them when user features span teams, contributing meaningfully to technical discussions Translate technical issues into customer experience impacts for both technical and non-technical stakeholders Provide timely, helpful feedback to peers and junior engineers through code reviews and test case audits Actively contribute to team knowledge sharing through documentation and presentations Participate in all Agile ceremonies with a focus on quality advocacy About you: 3-7 years of experience in software quality engineering, preferably in SaaS environments Strong demonstrated proficiency in Linux distributions and CLI-based testing, including log file analysis, and other troubleshooting tasks Experience with AWS or other major cloud platforms Basic Python/Shell (or similar) scripting knowledge with ability to edit existing scripts and create new automation Advanced skills with UI, API, and SQL testing methodologies Familiarity with test management tools such as TestRail or Qase Demonstrated experience leveraging Version Control Systems with a focus on Github and Bitbucket Experience with testing tools: Jira, Sentry, DataDog Understanding of containerization, Kubernetes, and CI/CD pipelines (Jenkins, CircleCI) Strong understanding of Agile/Scrum methodologies Proven track record of mentoring junior engineers and contributing to process improvements Excellent analytical and problem-solving abilities Strong communication skills with ability to present to both technical and non-technical stakeholders Most importantly: The courage to be vocal about quality concerns and testing impediments Demonstrated experience leveraging AI tools and technologies to improve workflows, enhance decision-making, or drive innovation. Additional Information The annual salary range for this position is $100,000 to $160,000. The salary range for performing this role outside of the US / Austin / California may differ. 8am is committed to offering competitive, fair and commensurate compensation and has provided an estimated pay range for this role. Actual compensation may vary based on job-related knowledge, skills, experience and education. Why 8am: At 8am, our culture is shaped by the people who bring it to life every day. Together, we build a company rooted in continuous learning, genuine community, holistic wellness, and meaningful engagement-values that empower us as individuals and unite us as a team. Our culture is grounded in our core values: Work Smart, Win Fast ; Outshine Ordinary , and We Find a Way . These values drive how we serve our customers and work with each other in a collaborative, inspiring, and empowering environment, every day. Here's how we support our 8Team: Health Insurance Coverage: We offer our 8Team a variety of medical, dental, and vision plans, designed to fit your needs, including a 100% company-paid HDHP plan for employees. Financial perks: We offer a competitive compensation and benefits package including annual bonuses, equity options and 401(k) or RRSP if in Canada, with a company match for all team members. Time for what matters: Flexible Time Off, paid holidays, and a parental leave program for our new parents. Wellness: Wellness stipends, mental health support, and one-on-one nutrition coaching. Learning and Development: Continuous learning through 8am.edu, leadership programs, professional development funds, and individually focused talent development. Giving back to the communities around us: Participate in our charitable matching gift program, paid time off for volunteer service, and company-sponsored volunteer events (both local and virtually). Engagement: Virtual and in-person team-building events, quarterly award recognition through our Rise & Shine Award of Excellence Program, and our peer-to-peer appreciation platform. At 8am, we don't just offer benefits - we create an environment where people can thrive, grow, and make a real impact every day. Diversity, equity & inclusion at 8am: At 8am, we recognize that innovation occurs with a strong team of people who are diverse in background, personality, talent and ideas. Experience comes in many forms and ensuring a diverse and inclusive workplace where we continue to learn from each other is an integral part of our culture. We are committed to creating a welcoming and transparent environment for all that embraces those differences through education, equal access to opportunities and information, inclusionary programs, and community outreach. Security advisory: Our hiring teams at 8am are dedicated to recruiting top talent that share our passion for serving the professional services industry through innovative financial technology. As such, our Talent Acquisition Team only follows legitimate hiring practices. We will always communicate with our candidates using emails with the 8am domain and will never ask for sensitive/personal data during the application process. All interviews take place over phone call, Zoom/Google Meet or in person. All offers are communicated verbally by our Talent Acquisition Specialists with a written offer letter as a follow up.

Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Job Summary As a Principal Quality Engineer, you will collaborate with the Quality Leadership team and other cross-functional individuals at all levels to ensure high levels of quality, safety and effectiveness are maintained thorough all phases of product realization in compliance with the corporate quality system, the QSR and the applicable ISO Standards. You will provide support to product development for product assurance and reliability testing, risk analysis, verification and validation activities, and manufacturing support. Essential Functions Ensure that the products are of high quality, safe, and effective at all stages of product realization process through the implementation and maintenance of an effective manufacturing quality assurance and quality control system Oversees product safety and reliability requirements. Participates in the assessment of product risk and works with engineers to implement and test risk mitigations Work with R&D on product development projects. Work with Manufacturing Engineering on product/process improvement projects. Works closely with software, mechanical, and electrical engineers to define system requirements Define a verification/validation requirements for hardware and software and develop protocols in conjunction with appropriate functions, perform analyses, and document results in a report format consistent with process requirements Investigate and analyze failures. Recommend and implement corrective and preventive measures as necessary Provide training and assistance to inspectors Develop, implement and maintain inspection and test methods for finished products and in coming components and materials. Evaluate precision and accuracy of testing, measurement and production equipment. Interpret engineering drawings, schematic diagrams, or formulas and confer with engineering staff to determine quality and reliability standards. Develop and analyze statistical data and product specifications to determine present standards and establish proposed quality expectancy of finished product. Recommend modifications of existing products, materials, or components to achieve the established quality standards and overall reliability standards Coordinate factory inspection by regulatory agencies certifying the products for electrical safety and EMC Perform inspection and testing of the products as assigned Required/Preferred Education and Experience Bachelor's Degree in Electrical Engineering or equivalent is required. Experience in the medical device industry in a Quality Engineering and or Test Engineering capacity is desired Minimum 3 years (Quality Engineer) or minimum 5-7 (Sr. Quality Engineer) or 7-10 years of experience in the medical device industry in a Quality Engineering capacity required Software controlled/electronic medical devices preferred Supplier Quality Assurance preferred Knowledge, Skills and Abilities Previous experience in Quality Engineering in medical device industry is a must Experienced in software controlled electrical and electro-mechanical devices is highly preferred. Exposure to sterile disposable products such catheters is preferred Hands-on experience with electrical, electro-mechanical and software verification and validation requirements is required. Understanding of sterilization process, environmental monitoring, biocompatibility requirements is a plus Quality System administration, and maintenance in the medical device industry Demonstrated experience/skill in risk analysis, failure analysis, and CAPA In depth knowledge of Design of Experiments, Process Capability Studies, Failure Mode, and Effects Analysis, Statistical Process Control, Industrial Statistical Methods and Lean Manufacturing Thorough knowledge of QSR and ISO 13485 (2003) requirements in a Class III environment Able to support development of products from initial concept to commercial product Knowledge of UL and IEC standards for device compliance Attention to detail, good organization, good interpersonal skills, good communication skills and ability to multitask Team player with strong customer orientation, proven leadership and technical skills Physical Demands 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. Standing - Occasionally Walking - Occasionally Sitting - Constantly Talking - Occasionally Hearing - Occasionally Repetitive Motions - Frequently ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. The annual salary for this position is: $170,000.00 to $198,700.00 This position is eligible for an annual bonus in accordance with the company's bonus plan. Factors which may affect starting salary include geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran.

Who we are With its A.I.-powered robotic technology platform, Symbotic is changing the way consumer goods move through the supply chain. Intelligent software orchestrates advanced robots in a high-density, end-to-end system - reinventing warehouse automation for increased efficiency, speed and flexibility. What we need Symbotic is seeking an experienced Principal Quality Engineer to work directly with our customer sites and installation teams to ensure quality standards are adhered to in all aspects of installations while acting as a catalyst for continuous improvement in our products and systems. This role will interface with install partners, equipment suppliers, sub-tiers, engineering, program team, and sourcing to drive high levels of quality and field reliability in critical sub-systems and components. The candidate must be able to understand the application of our products and their use environments to appropriately and strategically apply technical knowledge, tools and methodologies to drive installation quality. This position will require both a collaborative nature and ability to influence across organizational lanes at Symbotic, partners, suppliers, and customers. What we do The Principal Site Quality Engineer is part of the Quality team within the Manufacturing organization. The Quality team is responsible for ensuring quality across both supplier quality and install site quality. This role is specifically focused on site quality, partnering closely with install partners and vendors at the site level. The team drives continuous improvement practices that strengthen the performance and reliability of our systems, with a focus on maintaining consistency in the production and deployment of robots and automated systems that meet customer requirements and industry standards. Collaboration across departments is essential to embed quality throughout the product development, manufacturing, and installation lifecycle. What you'll do Provide Quality leadership at customer installation sites, focusing on identification and timely resolution of issues via structured quality methods. Oversee up to 3 Symbotic Installation sites simultaneously, providing training and oversight of a dedicated local QC resource (QCIT) at each site, ensuring all Quality surveillance and inspections are completed in a timely manner with issues and results effectively communicated to the site team and relevant Install Contractors. Provide surveillance of installation partners to ensure that all installation processes are complied with and critical to quality parameters adhered to. Plan, execute, and manage quality activities with suppliers & customer sites, setting a high standard so quality issues are prevented or minimized. Ensure that SCN's and RFI's are utilized effectively to facilitate timely completion of assigned scope and questions are resolved in a timely fashion. Employ 8-D based Corrective Action request to deliver efficient and effective root cause analysis and corrective / preventive actions that ensure there is no recurrence. Communicate issues across our operations team and drive closed loop problem resolution. Support Manufacturing and Quality Assurance with the disposition of discrepant material and the qualification of new material / processes to assure reliability requirements are met. Utilize Six Sigma and Lean methods to drive quality and process improvements. Utilize root cause methodologies to analyze product failures and develop corrective and preventive actions. Inspire others to share acquired knowledge and can take a supportive role during technical discussions. Mentor & coach site quality personnel to efficiently execute quality SOPs to identify and resolve issues. Regular travel required up to 75%. What you'll need B.S. Degree in Engineering or related discipline - M.S. degree a plus. Minimum of 15 years of Quality Engineering experience within a regulated manufacturing industry. Experience in all aspects of quality management: quality concepts/tools/methods (FMEA, DOE, MSA, GRR, 8D, etc.) Strong quantitative and analytic skills; capable of translating findings into business actions. Experience working in or with Engineering, Quality, Development Engineering, and Manufacturing. Strong process engineering fundamentals with the ability to identify critical control points. Strong hands-on project management and teamwork skills with demonstrated ability to consistently establish and meet aggressive timelines. Ability to build and maintain productive cross-functional relationships. Demonstrated ability to prioritize in a dynamic environment. Experience using Control Plans, FMEA's and PPAP or equivalent part approval process. Analytical problem-solving skills to determine root causes (8D, A3) and use of statistical analysis tools. Experience in reliability methods and failure mode analysis (DFMEA, PFMEA). Familiar with statistical process control software such as SAA, Minitab, and JMP and Mat lab. Advanced excel skills to organize and treat data. Tenacity to getting things done and not accepting the norm, being adaptable to constantly changing situations. Demonstrated experience at influencing and driving corrective action with large global suppliers. Excellent communication and negotiation skills with the ability to influence others. Able to work effectively with global, cross-functional stakeholders. Cross functional experience in Procurement and Supplier Relationship Management. Ability to present written and verbal presentations to engineering and manufacturing senior management. CQE, Six Sigma Black Belt preferred (must show deep core knowledge). Certified or previously certified auditor for ISO 9001, AS9100, etc. preferred. Our Environment Remote, field-based position. Approximately 75% of time will be spent on a construction sites with PPE required (hard hat, safety vest, steel toes, eyeglasses, ear protection, fall protection (e.g., safety harness). Employee must have a valid driver's license and the ability to drive and/or fly to client and other customer locations. Our main office is in Wilmington, MA. The person taking this position will be required to perform work at our customer installation locations for extended periods of time where equipment is installed and ready for commissioning. Easy access to a major airport a must. The employee is responsible for owning a credit card and managing expenses personally to be reimbursed on a bi-weekly basis. The employee is frequently required to walk and reach with hands and arms. The employee is routinely required to work at heights of up to 45 feet and within restrictive areas of 24 inches. to stand; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 50 pounds. Must comply with all safety requirements and protocols, including without limitation Lock out tag out safety protocols and fall protection safety protocols. There will be steep stairs to climb into the structure. You may be required to routinely walk up and down stairs to navigate the automation structure. You will regularly be near railings that are high off the ground. Subject to environmental conditions, protection from weather conditions but not necessarily temperature changes. Must be capable of working in temperatures ranging from 105° to 32° Fahrenheit. #LI-TS1 #LI-Remote About Symbotic Symbotic is an automation technology leader reimagining the supply chain with its end-to-end, AI-powered robotic and software platform. Symbotic reinvents the warehouse as a strategic asset for the world's largest retail, wholesale, and food & beverage companies. Applying next-gen technology, high-density storage and machine learning to solve today's complex distribution challenges, Symbotic enables companies to move goods with unmatched speed, agility, accuracy and efficiency. As the backbone of commerce the Symbotic platform transforms the flow of goods and the economics of supply chain for its customers. For more information, visit ***************** We are a community of innovators, collaborators and pioneers who embrace our differences, because we know unique perspectives make us stronger and smarter. Every perspective matters. We depend on the collective voices of our employees, customers and community to help guide us as we build a better place to work - for you and the world. That's why we're proud to be an equal opportunity employer. We do not discriminate based on race, color, ethnicity, ancestry, religion, sex, national origin, sexual orientation, age, citizenship status, marital status, disability, gender identity, gender expression, veteran status, or genetic information. The base range for this position in the posted location is $130,000.00 - $206,800.00 however, base pay offered may vary depending on job-related knowledge, skills, and experience. The compensation package includes medical, dental, vision, disability, 401K, PTO and/or other benefits.

On behalf of VetJobs/MilitarySpouseJobs, thank you for your interest. We are assisting our partnering company, listed below, with this position. It is open to Veterans, Transitioning Military, National Guard Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow for next steps. Requisition Number: 25067 Company: Westinghouse Electric Co Location: Cranberry Township, US Are you interested in being part of an innovative team that supports Westinghouse's mission to provide clean energy solutions? At Westinghouse, we recognize that our employees are our most valuable asset and we seek to identify, attract and recruit the most qualified talent while recognizing and encouraging the value of diversity in the global workplace. About the role: As a Principal Supplier Quality Engineer you will lead others in multiple quality assurance tasks to ensure externally sourced products meet the quality and technical requirements defined by Westinghouse. Within this role the primary focus will be to manage teams in the execution of complex plans for supplier program development, oversight, and quality verification activities. You will report to the Manager, Supplier Quality Assessments. This is a remote position. Travel of 40-50% is required for this role. Key Responsibilities: Develop and implement supplier surveillance and oversight plans for complex and first of a kind procurements to ensure compliance with quality and technical standards. Lead teams in the resolution of complex supplier quality issues which adversely impact product quality. Monitor progress and direct teams to achieve established quality goals within budgetary and schedule constraints. Create certification documents, which identify the procurement requirements met by the purchased material or equipment, such as codes, standards, and other specifications imposed by Westinghouse Customers, for major equipment and components. Lead assessments of the global supply base to ensure compliance with applicable regulations, codes and standards. Evaluate supplier quality plans, procedures, and processes to verify compliance to quality and technical requirements defined by Westinghouse Engineering Apply advanced quality control techniques and statistical methods for collection of deficiency information to identify failure causes and trends, rate performance and measure the effectiveness of supplier QA programs, and internal processes. Write detailed segments of QA plans/programs according to current U.S. Nuclear Regulatory Commission (NRC), Westinghouse and customer QA standards for nuclear and non nuclear facilities. Implement policies on scope and retention requirements of quality assurance documentation. Qualifications: 5 or more years of experience is required. An NQA-1 Certified Lead Auditor certification is desirable. A bachelor's degree in an engineering discipline, technical area or equivalent is required. Capability to concisely explain QA procedures to internal personnel and external customers, subcontractors, suppliers and licensees relative to Westinghouse quality related products and services. You develop solutions, plan work and set priorities while using a questioning attitude to identify risks. Exceed customers' expectations in ways that are in consideration of our goals. We are committed to transparency and equity in all of our people practices. The base salary range for thisposition, which is dependent upon experience, qualifications and skills, is estimated to be $103,200 to $129,000 per year. #LI-Remote Why Westinghouse? Westinghouse offers competitive benefits to all our employees around the globe to keep them healthy and enhance their well-being. In the U.S. the following are representative of what we offer: Competitive Salary Comprehensive Health, Wellness and Income Protection Benefits Employee Assistance Program: confidential counseling and resources for employees, eligible dependents, and household members 401(k) Savings Plan with Company Match Paid Vacations and Holidays Opportunities for Flexible Work Arrangements Educational Reimbursement Program Employee Referral Program Westinghouse Electric Company is the global nuclear energy industry's first choice for safe, clean, and efficient energy solutions. We enable our delivery of this vision by living our value system: Safety and Quality Integrity and Trust Customer Focus and Innovation Speed and Passion to Win Teamwork and Accountability While our Global Headquarters are located in Cranberry Township, PA, we have over 11,000 employees working at locations in 19 different countries. You can learn more by visiting *********************************** Westinghouse is an Equal Opportunity Employer including Veterans and Individuals with Disabilities Get connected with Westinghouse on social media: Twitter | Facebook | LinkedIn| YouTube Employment opportunities may require access to information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States.

Your Mission As the first engineer dedicated to quality, you will establish the foundation for how we validate AI driven systems. Quality is already integrated across engineering, and this role advances it by introducing new methodologies and defining the long term quality roadmap. While overall product quality is a shared responsibility, you will elevate the entire engineering organization so that strong quality practices scale with the product. This role provides the opportunity to work on cutting-edge software solutions while driving quality improvements What you'll do Quality Engineering Strategy: Designing and maintaining testing systems for deterministic logic and AI influenced, non deterministic behavior, integrating these validations directly into CI, release pipelines, and review workflows Collaboration and Shift Left: Engaging early with engineering to surface risks before implementation, strengthening team wide quality skills, and promoting testability as a core design requirement Test Methodology Expansion: Broadening our verification approach beyond unit tests into integration, system, stress, and full workflow testing across the entire stack Environment Readiness: Maintaining dependable test environments with strong instrumentation for rapid diagnosis, enhancing observability and logging to shorten the path from failure to root cause Data and Tooling: Building tools, fixtures, and supporting libraries that generate stable and repeatable test conditions, enabling reliable validation of complex scenarios without ad hoc data creation Required Qualifications 5+ years experience in software quality engineering, test engineering, or a closely related discipline Strong investigative instincts and a deep interest in understanding failures, identifying root causes, and preventing recurrence Skill in isolating external dependencies during integration tests by mocking third party services using custom code or established tools Proficiency with Python and modern test frameworks within container based environments Demonstrated success designing automated test suites across multiple layers of a contemporary application stack Experience working within fully containerized development and execution workflows Being data-driven is part of your DNA Early-stage startup mindset. You thrive on ambiguity and move with lightspeed execution Desired Qualifications Experience with cloud based monitoring and metrics platforms such as Prometheus, Grafana, or CloudWatch Background with container orchestration and deployment systems including Kubernetes, GitLab pipelines, or ArgoCD Familiarity with modern frontend technologies, particularly React and TypeScript Interest or experience in security focused testing and broader cybersecurity practices Ability to thrive in a rapidly evolving startup environment Comfort using AI assisted coding and development tools Work Environment/Travel We are a 100% remote company where you will work from your home with company-provided equipment to set you up for success. Semi-frequent travel to professional office settings and other events locally and nationally; some overnight travel expected. Compensation In the spirit of pay transparency, we are excited to share the base salary range below, exclusive of fringe benefits or potential bonuses. If you are hired at Dropzone your final base salary compensation will be determined based on factors such as geographic location, skills, education, and/or experience. In addition to those factors, we believe in the importance of pay equity and consider internal equity of our current team members as a part of any final offer. Please keep in mind that hiring at the maximum of the range would not be typical to allow for future and continued salary growth. We also offer a generous benefits package, including company paid health insurance, 401K Plan with employer match, Self-Managed PTO, parental leave, and more.

At Prime Therapeutics (Prime), we are a different kind of PBM, with a purpose beyond profits and a unique ability to connect care for those we serve. Looking for a purpose-driven career? Come build the future of pharmacy with us. Job Posting TitleQuality Engineer IT Principal - Client Implementation - RemoteJob Description The Quality Engineer IT Principal plays a pivotal role delivering implementation testing leadership based in the quality engineering organization with responsibilities spanning multiple products and industry sectors. The ideal candidate is a strategic quality leader with proven experience interfacing with executive stakeholders, third-party vendors, and clients. This role is responsible for incorporating quality shared services such as test frameworks, test data management, performance engineering, metrics, and testing practices inclusive of the tools that support these activities. This position partners with product teams to enable quality plans, and participates in ongoing internal training, provides consulting services, and supports staffing tasks. In addition, this role leads cross-functional teams to provide solutions for specific needs. Responsibilities Define, communicate, and report status on the Quality Shared Services roadmap Interface with executive leadership, external clients, and vendor partners to align quality strategies with Implementation objectives. Define the Quality strategy for Implementations; provide guidance, best practices, leadership and supervisory oversight to product teams in scope Lead Community of Practice (CoP) Provide clear, data-driven insights into Implementation testing performance via metrics, dashboards, and reporting frameworks. Lead teams in design, development, and deployment of Quality capabilities; coordinate initiatives across departments and portfolios Lead/Participate Quality Excellence Center (QEC) activities for metrics, training, recruiting, staffing, and career planning activities Other duties as assigned Minimum Qualifications Bachelor's degree in information technology or related area of study, or equivalent combination of education and/or relevant work experience; HS diploma or GED is required 8 years of experience in software testing including software automation Must be eligible to work in the United States without need for work visa or residency sponsorship Must be eligible to work in the United States without the need for work visa or residency sponsorship Additional Qualifications Proven experience in quality engineering leadership, ideally in healthcare, insurance, or regulated industries Exceptional communication and stakeholder management skills --- able to influence internal leadership and external client partners Advanced ability in writing proposals and quality assurance testing reports; presentation skills Ability to work in a fast-paced environment with tight deadlines and changing priorities Ability to work independently on multiple concurrent projects and manage priorities Advanced knowledge of testing practices, methods, standards, and tools Proficient in leveraging test management tools to include reports and dashboards Ability to design, develop, coordinate, and document needed testing capabilities required for complex/integrated business solutions Preferred Qualifications Experience with enterprise tooling: CI/CD pipelines (e.g. Jenkins, GitHub Actions), containerization (e.g. Docker, Kubernetes), and cloud platforms (e.g. AWS, Azure, GCP) Experience with Test Data Management, test automation and/or performance testing Experience writing QA/Testing related proposals, presentations, and status reports Certification in software testing or quality assurance Experience driving and/or maintaining IT department technical improvements, initiatives Every employee must understand, comply with and attest to the security responsibilities and security controls unique to their job, and comply with all applicable legal, regulatory, and contractual requirements and internal policies and procedures Every employee must be able to perform the essential functions of the job and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions, absent undue hardship. In addition, Prime retains the right to change or assign other duties to this job. Potential pay for this position ranges from $108,000.00 - $184,000.00 based on experience and skills.To review our Benefits, Incentives and Additional Compensation, visit our Benefits Page and click on the "Benefits at a glance" button for more detail. Prime Therapeutics LLC is proud to be an equal opportunity and affirmative action employer. We encourage diverse candidates to apply, and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sex (including pregnancy), national origin, disability, age, veteran status, or any other legally protected class under federal, state, or local law. We welcome people of different backgrounds, experiences, abilities, and perspectives including qualified applicants with arrest and conviction records and any qualified applicants requiring reasonable accommodations in accordance with the law. Prime Therapeutics LLC is a Tobacco-Free Workplace employer. Positions will be posted for a minimum of five consecutive workdays.

Senior Quality Engineer Company: VB Spine Looking for a career where your work truly matters? At VB Spine, you'll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We're seeking a detail-oriented, driven Senior Quality Engineer to provide leadership in quality assurance, control, and preventive activities. In this role, you'll manage quality activities for internal and external suppliers, support process development, verification, validation, and product transfer, and ensure compliance with medical device regulations and industry standards. What You'll Do: Partner with Operations and other business functions to ensure quality performance of products and processes. Serve as the Quality representative on cross-functional teams to address key quality issues. Support compliance to evolving standards and regulatory changes through the development and improvement of SOPs, work instructions, and procedures. Evaluate and manage internal and supplier change management activities. Apply risk management principles to manufacturing operations. Lead internal and supplier-driven non-conformances, CAPA investigations, and timely closures. Act as subject matter expert during internal and external audits, including front and backroom support. Disposition non-conforming product within the Material Review Board (MRB). Monitor and analyze KPIs to drive corrective actions and quality improvements. Collaborate with stakeholders to certify supplier parts and develop inspection methods. Conduct supplier control activities including audits, supplier file maintenance, and Approved Supplier List (ASL) updates. Support manufacturing process development and improvement efforts. Lead part approval activities for new products and changes. Execute quality deliverables for engineering changes, product transfers, and supplier-initiated changes. Lead containment activities for potential product escapes. Support manufacturing-related complaints and product field actions. Review, execute, and approve validation protocols and reports for equipment, processes, MSA, and software. Collaborate with Regulatory to develop and revise Instructions for Use (IFUs). Review and approve quality records. Apply statistical analysis and process control methods to support CAPAs and management reviews. Provide GMP training, onboarding, and other quality-related training as needed. Support new product development and changes to existing products and processes. What You Bring: Bachelor's degree required; Engineering discipline preferred (Biomedical, Process, or Mechanical Engineering recommended). Minimum 3 years' experience in a quality role within a medical device company (or equivalent regulated manufacturing experience). Professional certification in a quality discipline (e.g., Lead Auditor, CQE, CRE, Six Sigma) highly desirable. Knowledge of quality concepts such as Risk Management, CAPA, Audits, and Statistics. Understanding of applicable regulations (ISO 13485, FDA QSR, EU MDR) desired. Experience interacting with regulatory agencies (FDA, MoH, TUV, etc.). Skills in formal investigation, root cause analysis, and process improvement preferred. Process-based auditing experience preferred. Ability to interpret engineering drawings and technical specifications. Strong project management skills and the ability to influence without authority. Why VB Spine? We believe in growing talent from within. At VB Spine, you'll join a high-performing team, benefit from mentorship at all levels, and play a key role in advancing innovation in spinal care. Your work will have a direct impact on patient safety and surgical success. Compensation: Pay for this role is competitive and based on experience. Final compensation is determined on a case-by-case basis, considering skills, experience, and market conditions. Benefits include: Comprehensive health, dental, and vision insurance 401(k) with company match Paid time off (PTO) and holidays Ongoing training and professional development opportunities Opportunities to grow within a fast-paced, dynamic company

CIS Secure will be leading a multi-year program in partnership with an industry Integrator to deliver a next-generation secure communication system for aircraft operations. Based in Ashburn, VA, this initiative will produce a ruggedized, military-grade VOIP solution that enables secure voice and data communication across multiple classified domains. The program spans the full engineering lifecycle, from requirements analysis and preliminary design through prototyping, integration, and verification testing, executed under AS6500, AS9100, and CMMI standards. The Senior Quality Engineer will serve as a main figure in the development and optimization of quality control processes. This effort offers an opportunity to help shape a program from the ground up and build a technical framework that will define long-term success. At CIS Secure, you'll be part of a mission-driven team that designs and delivers cutting-edge, secure communications products for government and commercial clients. We offer a collaborative work environment, competitive benefits, and the opportunity to make a real impact in national security and secure tech innovation. Come join one of Washington's Best Places 2022 to work and do good work for a great purpose! About CIS Secure Computing, Inc. CIS Secure Computing, Inc. is a company that specializes in custom solutions of secure communications equipment. Our primary customers include organizations within the defense, intelligence, law enforcement, and homeland security communities whose missions depend heavily on their ability to communicate and exchange information in a secure manner and to operate in challenging physical environments. CIS Secure Computing, Inc. serves the secure communications market as a leading provider of communications and computing solutions for government and commercial customers. CIS designs and manufactures a wide range of products, which include secure telephones (under the TSG protocol), secure computers, encrypted tactical communication systems, secure tele- and video-conferencing systems, and a variety of specialty systems used in secure networks. Responsibilities The Senior Quality Engineer will be responsible for the duties and responsibilities outlined below, as well as additional tasks as assigned: * Lead complex investigations, root cause analysis, and corrective actions. * Develop and optimize quality control processes, test methodologies, and inspection systems. * Drive continuous improvement projects (Lean, Six Sigma, Kaizen). * Lead supplier audits, qualification, and corrective action programs. * Train and mentor junior engineers and inspectors. * Interface directly with customers, certification bodies, and regulatory agencies. OPERATING HOURS AND EXPECTATIONS: * This position anticipates on-site work with regular hours, Monday-Friday. Occasional telework may be considered and will be discussed as a part of the interview process. WORK LOCATION AND TRAVEL: * Primary work location will be the CIS Secure headquarters located in Ashburn, VA. Minimal local travel is anticipated for this position. Qualifications CLEARANCE: * All candidates must be a US Citizen or permanent resident at the the time of application. * All candidates must be clearable, an active and current DoD Secret clearance is desired. EDUCATION: * Bachelor's degree in Engineering, or related field; or an equivalent combination of education, certifications and related work experience. * Masters degree, desired. CERTIFICATION(S): * ASQ Certified Quality Engineer. * Lean Six Sigma, preferred. REQUIRED SKILLS AND EXPERIENCE: * Ten or more (10+) years of progressively responsible experience in quality engineering, manufacturing engineering, or process improvement within a production or assembly environment. * Experience leading root cause analysis, corrective/preventive action (CAPA), and continuous improvement initiatives. * In depth knowledge of ISO 9001:2015 * Familiarity with AS9100 and AS6500 Standards. DESIRED SKILLS AND EXPERIENCE: * Hands-on experience with supplier quality management, process validation, or new product introduction (NPI). * Knowledge of reliability testing, environmental stress screening (ESS), or regulatory compliance for specific industries. PHYSICAL DEMANDS: * While performing the duties of this job, the employee is regularly required to walk; sit; use hands to finger, handle, or feel and talk or hear. The employee is frequently required to stand; reach with hands and arms and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds assisted and unassisted. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. * Ability to travel, fly and/or drive a car for client visits. WORK ENVIRONMENT: * The noise level in the work environment is usually low to moderate. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Benefits WHAT WE OFFER: At CIS Secure and its associated companies, Intrepid Solutions and Services and Darkblade Systems, we believe in promoting fair and transparent pay practices. We are committed to disclosing the compensation range for transparency and to set clear expectations for all applicants for this posting. This range represents the anticipated low and high end of the base salary for the advertised job, promotion, or transfer opportunity. Please note that the pay range provided is a good faith estimate for the position at the time of posting. The actual salary offered may vary based on various factors including but not limited to relevant experience, knowledge, skills and abilities, education, geographic location, as well as internal equity, and alignment to market data.Job Type: Full-time (Onsite) Pay Range: $130,000.00 - $170,000.00 per year Benefits: * 401(k) with company matching * Dental insurance * Medical insurance (Four plan options) * Health Savings Account option (with company contribution) * Flexible Spending Account * Vision Insurance * Life and Disability Insurance * Ancillary offerings (Hospital Indemnity, Accident, Critical Illness, Pet Insurance) * Paid Time Off * Holiday pay CIS Secure and it's associated companies, Intrepid Solutions and Darkblade Systems, is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class.

Movius is revolutionizing the way businesses communicate. We are the leading global provider of secure, cloud-based mobile communications. Our MultiLine solution enhances workflows, resolves compliance gaps and unifies cross-channel messaging. Movius AI-powered solutions enable businesses to build strong and lasting relationships with their customers in a company-owned, controllable system. In today's on-the-go world, wave goodbye to excessive hardware costs and IT overhead. Welcome to Phone 3.0. Headquartered in Alpharetta, GA, with offices in Bangalore, India, and London, Movius partners with leading global wireless carriers like T-Mobile, BT, Singtel & more. To learn more about Movius, visit ************* Responsibilities: * Implement strategy, technology, process and human capital capable of supporting the development of scalable, functional and reliable product software. * Focus on innovation, emerging technologies and making recommendations on the strategic use of technology for leveraging business results. Requirements: * Bachelor's or Master's Degree in Computer Science, Engineering or related field * 7 years of building Voice based applications, LAN/WAN experience, design and troubleshooting. * Experience building voicemail systems * Hands on R&D experience with VoIP, SIP, RTP is required. * Strong programming skills in C, C++, and Python. * Experience with development for Asterisk and Kamailio stack is required. * Experience with SBC, PBX for real time communication applications is a huge plus. * Experience developing, deploying and operating VoIP monitoring, reporting and alerting systems. * Linux/Unix understanding and ability to navigate through a system, look at logs, etc. * Highly analytical and detail oriented * Excellent verbal and written communication skills. * Experience with virtualization and cloud computing. * Passion for DevOps and continuous delivery a plus.

Thales Defense & Security, Inc. (TDSI) Headquartered in Clarksburg, MD, is a U.S. company that has been serving domestic and international defense Air, Land and Sea domains for 60+ years. With over 1,000 employees, TDSI and its four subsidiaries (Advanced Acoustic Concepts, Digital Receiver Technology, Tampa Microwave, and Trusted Cyber Technologies), supports U.S. Joint Services, special operations forces and multi-national partners with a variety of communication, visualization, signal intelligence/electronic warfare, and sensor/sonar capabilities. TDSI's key technologies include tactical handheld radios, expeditionary satellite terminals, helmet-mounted displays, optics and target recognition capability, advanced radars, undersea sensing and missile systems. Lives depend on what we do! Top Benefits (Subject to terms of applicable policies/plans) * Competitive Salary * Yearly Incentive Compensation Plan * Medical insurance for self and eligible family members * Generous 401(k) program- up to 7% company contribution and 100% immediate vesting * Tuition Reimbursement * Paid wellness, vacation, and holiday leave * Paid maternity, paternity, and parental leave * 9/80 Work Schedule (every other Friday off) We currently have an opening for a Senior Quality Engineer at our Germantown, MD campus, focused on our DRT (Digital Receiver Technology) product line. This position reports to the Quality Engineering Manager at TDSI in Clarksburg, MD. Responsibilities * Supports the TDSI AS9100 Quality Management System (QMS). * Leads Quality Engineering activities throughout the product life cycle to include contract review, requirements management, design reviews, verification / validation, and release to production. * Initiates and drives internal Corrective Actions Requests (CARs) as required. * Assists Supply Chain Quality Assurance activities to include approving / auditing suppliers, conducting Source Inspections of Hardware / Software and supporting Supplier Corrective Action Request (SCARs). * Provides interface between Purchasing, Engineering, Program Management, and Manufacturing departments during transition of new products from the design phase to the production phase. * Supports Program Quality Assurance activities for production programs to include First Article Inspections (FAI), Material Review Board (MRB), Change Control Board (CCB), Failure Review Board (FRB), and Work Product review and approval. * Manages high-priority tasks of multiple projects simultaneously in development. * Develops Inspection Plans and processes for Receiving and Final Inspection activities. * Determines Process Capability (Cpk) and defect trends based on statistical analysis. * Supports Continuous Improvements initiatives. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * U.S. Citizenship required. - Applicants selected may be subject to a government security investigation and must meet eligibility requirements for access to classified information. * BS Mechanical/ Electrical Engineering or equivalent/related technical degree or experience. * 5+ years of Quality Engineering experience. * Proficient in ASME / ANSI Y14.5 with demonstrated ability to read mechanical drawings. * Demonstrated knowledge of electro-mechanical assemblies, IPC standards as well as familiarity with schematics and RF Test equipment. * Knowledgeable in elements of Software Quality Assurance, automated MRP systems, Cause / Corrective Action systems. * Excellent English communication skills - written and oral. * Proficiency in Enterprise Resource Planning (ERP) systems. * Proficiency in Requirements and Configuration Management tools. * Proficiency in Microsoft Office Products. * Proficiency in Minitab. * Efficiency in SAP and/or CostPoint preferred. * AS9100/ CMMI experience a plus. * Ability to travel up to 10% of time domestically. * Ability to follow and comply with all Company policies, procedures and guidelines including the Compliance Policy Manual and the Code of Ethics. The annualized pay range for this role is $99,995.00 - $127,771.00 USD along with a target incentive compensation plan (ICP) of 5%. The pay range provided is a good faith estimate representative of the experience level for the role described above. TDSI considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. For specific questions about this job posting, candidates may contact Talent Acquisition at *********************. Thales Defense & Security, Inc. is committed to non-discrimination as applicable under federal, state and local laws. We are an E-Verify Employer. If you need an accommodation or assistance in order to apply for a position with Thales Defense & Security, Inc., please call Human Resources at ************. #LI-JK1 #LI-ONSITE

Here at Appian, our values of Intensity and Excellence define who we are. We set high standards and live up to them, ensuring that everything we do is done with care and quality. We approach every challenge with ambition and commitment, holding ourselves and each other accountable to achieve the best results. When you join Appian, you'll be part of a passionate team dedicated to accomplishing hard things, together. We're passionate about technology. We love making it, and we love using it. We want to revolutionize the way people work, and in doing so, we develop the product to be simple so our customers can thrive. Joining Appian Engineering will provide you with the opportunity to learn in an environment that values cross-functional collaboration and is committed to personal and professional growth. Senior Quality Engineers ensure the high quality and timely delivery of our software to customers. They serve as champions for the customer perspective - ensuring that quality is embedded into every stage of the development process. With a strong understanding of complex system interactions and dependencies, they proactively identify potential risks and work cross-functionally to address them through thoughtful design and rigorous testing. Senior Quality Engineers analyze defects and delivery gaps to drive continuous improvement, ensuring issues are not repeated and our standards of excellence are consistently upheld. This role is based at our Headquarters in McLean, Virginia. Appian was built on a culture of in-person collaboration, which we believe is a key driver of our mission to be the best. Employees hired for this position are expected to be in the office 5 days a week to foster that culture and ensure we continue to thrive through shared ideas and teamwork. We believe being in the office provides more opportunities to come together and celebrate working with the exceptional people across Appian. To be successful in this role, you will: Manually test and troubleshoot new features from a multitude of dimensions: systems integration, GUI, Compatibility, User Acceptance Testing, functionality, database, and regression Test features across web, Android and iOS platforms Write automated test code using tools like Java, Python and Selenium. Ability to apply test automation design and techniques Support existing features by performing regression testing when bugs are resolved Perform analysis, research, and troubleshooting of software defects and aid in the documentation of defects and anomalies Build, maintain and improve test artifacts for rapid and efficient reuse by the Test Engineering team Work with other scrum team members to define and review Acceptance Criteria. Ensure complete and timely reporting of bugs and test results Know some elements of test design Understand how to systematically analyze requirements Know how to understand the root cause of software defects Understand Engineering strategy for performance engineering Write complete and concise software defects with all necessary supporting information Participate in release management activities Basic Qualifications: B.S. degree in an Engineering field or demonstrated aptitude for technology 5 - 10+ year of relevant experience Preferred Qualifications: Understand and Test the unique and complex behavior of AI and machine learning models. Tools and Resources Training and Development: During onboarding, we focus on equipping new hires with the skills and knowledge for success through department-specific training. Continuous learning is a central focus at Appian, with dedicated mentorship and the First-Friend program being widely utilized resources for new hires. Growth Opportunities: Appian provides a diverse array of growth and development opportunities, including our leadership program tailored for new and aspiring managers, a comprehensive library of specialized department training through Appian University, skills based training, and tuition reimbursement for those aiming to advance their education. This commitment ensures that employees have access to a holistic range of development opportunities. Community: We'll immerse you into our community rooted in respect starting on day one. Appian fosters inclusivity through our 8 employee-led affinity groups. These groups help employees build stronger internal and external networks by planning social, educational, and outreach activities to connect with Appianites and larger initiatives throughout the company. About Appian Appian is a software company that automates business processes. The Appian AI-Powered Process Platform includes everything you need to design, automate, and optimize even the most complex processes, from start to finish. The world's most innovative organizations trust Appian to improve their workflows, unify data, and optimize operations-resulting in better growth and superior customer experiences. For more information, visit appian.com. [Nasdaq: APPN] Follow Appian: LinkedIn. Appian is an equal opportunity employer that strives to attract and retain the best talent. All qualified applicants will receive consideration for employment without regard to any characteristic protected by applicable federal, state, or local law. Appian provides reasonable accommodations to applicants in accordance with all applicable laws. If you need a reasonable accommodation for any part of the employment process, please contact us by email at ReasonableAccommodations@appian.com. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Appian's Applicant & Candidate Privacy Notice

Blue Energy's mission is to unlock energy abundance, energy affordability, energy security, and turn-key decarbonization by developing the fastest path to deploying new nuclear MWs at scale. We are utilizing shipyard manufacturing supply chains and techniques from offshore oil and wind to reduce the cost of nuclear plants by over 60% and the manufacturing timeline to 24 months. Blue Energy is a platform technology that makes use of the latest NRC-approved reactors and is in negotiations with existing nuclear and industrial sites, enabling a much faster regulatory pathway to deploy our first unit. With our innovative centralized shipyard manufacturing approach, we can put nuclear power on a cost-reduction learning curve akin to wind, solar, and lithium-ion batteries. Role Summary The Senior Quality Engineer reports to the Corporate Director of Quality. The role will be assisting in development and implementation of the entirety of Blue Energy's nuclear Quality Assurance Program. Performing program maintenance and providing support for Blue Energy's staff and external organizations on all topics related to Blue Energy Quality Assurance. Key Responsibilities Model excellence by demonstrating the highest standards and values in work and promoting them within the organization and externally Assist in developing a greenfield nuclear Quality Assurance Program Provide quality program oversight, compliance and guidance as required while maintaining appropriate independence Creating procedures for Quality Assurance (QA) and other departments as they relate to quality Develop or assist in creating and implementing a Corrective Action Program Assist in developing and implementing a document and records management program Assist in developing and providing training on QA-related topics and assists in the resolution of quality-related problems Assists in ensuring Blue Energy staff understand quality requirements and how these requirements apply to their work Reviews procurement documents to ensure appropriate quality controls are specified Perform independent QA assessments/audits to ensure project QA plans are properly executed and evaluates the effectiveness of controls delineated in these plans Supports management and staff with QA services, as requested Assists in developing supply chain and providing supplier oversight and support Perform supplier qualification audits Qualifications Must possess the ability to function well in a fast-paced, developmental environment and be able make decisions based on developing information Extensive knowledge of Quality standards, as a minimum, 10 CFR 50 Appendix B, ASME NQA-1, ASME III and ISO 9001 10 years of experience working in a Nuclear Regulatory Commission (NRC) compliant quality assurance program 5 years of experience managing a nuclear quality assurance program or a division of a program Experience writing procedures Excellent verbal and written communication skills Experience with manufacturing processes Ability to be qualified as an NQA-1 Lead Auditor Preferred Qualifications NQA-1 Lead Auditor Experience in a “start-up” organization or environment Certification or accreditation as a trainer Formal technical training (degree program, trade school, certification) Experience working with or developing QA software management systems We look forward to your application and helping foster an era of safe, clean, affordable, and abundant energy. Blue Energy is dedicated to building a diverse and inclusive workplace. If you're excited about this role but your experience doesn't perfectly align with every requirement, we encourage you to apply anyway. You might be the right candidate for this or other roles at Blue Energy now or in the future.