Quality Control Specialist

🏢 Summary: Quality Control Specialist role in a medical device manufacturing environment focused on receiving, in-process, and final inspections for catheter-based cardiovascular products. The position supports quality systems, nonconforming product reviews, equipment calibration, environmental monitoring, and lot release activities in an in-office setting. The offer includes competitive pay, equity opportunities, comprehensive benefits, and professional growth during company expansion. 🗂️ Requirements: High school diploma or equivalent, 2+ years of hands-on quality inspection experience in medical device manufacturing, Proficiency with word processing software, Proficiency with spreadsheet software, Full professional proficiency in English, Experience performing receiving, in-process, and final inspections, Ability to document nonconforming products, Ability to maintain traceability and quality system records 📃 Skills: QC, Inspection, Calibration, Monitoring, NCR, NCMR, CAPA, Traceability, Sampling, Microscopes, Excel, Word 🏢 Description: Company Summary: Join a team that's redefining what's possible in cardiovascular treatment. At Jupiter Endovascular, we're revolutionizing catheter-based therapies by bringing the precision and control of surgery to minimally invasive procedures. For decades, catheters have remained largely unchanged—rigid, unstable, and difficult to maneuver through the body's winding anatomy. We've developed a transforming fixation technology that navigates flexibly through the vascular system, then locks into place to deliver treatment with surgical-like stability and control. Our device solves one of the longest-standing challenges in endovascular procedures, empowering physicians and improving outcomes for millions of patients living with cardiovascular disease. We're entering an exciting new phase—scaling up production, expanding our team, and preparing for commercial launch. Founded and headquartered in Menlo Park, California, Jupiter Endovascular is led by a proven team of medical device entrepreneurs and backed by top-tier investors across venture capital, private equity, and strategic partners. We've built a fast-paced, collaborative culture grounded in innovation, teamwork, and purpose. Every role at Jupiter directly contributes to our mission: saving lives by advancing the future of endovascular therapy. Position Overview: The Quality Control Specialist is primarily responsible for receiving, in-process, and final product inspections. The QC Specialist may also perform equipment calibration and maintenance coordination and environmental monitoring activities in accordance with established quality system procedures. This role also supports nonconforming product disposition, traceability, lot release, and other quality assurance activities as assigned. This is an in-office role. Responsibilities: - Perform product receiving, in-process, and final inspections in accordance with written procedures, statistical sampling plans, engineering drawings, and product specifications, documenting nonconforming products as appropriate. - May administer the equipment calibration and maintenance system, environmental monitoring program, and bioburden monitoring program, including coordination with subcontracted service providers. - Coordinate or lead nonconforming product reviews, including Material Review Board activities and NCR/NCMR disposition, to support timely product decisions. - Maintain quality system logs, records, and filing systems, and ensure accurate traceability of components and finished products. - Maintain and operate inspection and test equipment, and provide input on inspection methods and quality procedures. - Support corrective and preventive action activities, supplier evaluations, and supplier performance monitoring. - Review product lot history records and support lot release to finished goods inventory, as applicable. - Support finished goods shipping and commercial release activities, as applicable. - Contribute to improvements in quality system procedures and work instructions related to areas of responsibility. - Train and advise other employees on quality-related requirements and ensure effective communication across functions. - Represent areas of responsibility during internal and external quality audits and support audit readiness. Qualifications: - High school diploma or equivalent required. - Minimum of two years of experience with hands on quality inspection in a medical device manufacturing environment required. - Startup or small-company experience preferred. - Catheter manufacturing experience preferred. - Proficiency with word processing and spreadsheet software required. - Full professional proficiency in English required. Preferred Qualifications: - Experience reading and interpreting engineering drawings, specifications, and statistical sampling plans. - Experience using dimensional and visual inspection equipment, including microscopes. - Strong hand-eye coordination, manual dexterity, color vision, and visual acuity, corrected if necessary. - Ability to work under pressure, manage multiple deadlines, and maintain effective working relationships. - Strong attention to detail, organizational skills, and oral and written communication skills. Why Jupiter Endovascular? - Work in a culture built on shared purpose, where passionate teammates support one another and stay motivated by improving patient lives. - Thrive in a collaborative environment that values new ideas, gives everyone a voice, and offers professional growth and exposure across departments as the company enters an exciting phase of expansion. - Earn competitive pay with performance incentives and equity opportunities. - Enjoy comprehensive, top of the market medical, dental, and vision coverage focused on meaningful premium support and smart savings. - Access meaningful benefits including a top tier 401(k) with a best in-class plan design which includes strong employer contributions, short and long-term disability, life insurance, commuter benefits, and wellness support. - Take advantage of a healthy paid time off policy, company holidays, and an environment that encourages a healthy work-life balance. - Strengthen relationships through shared experiences - from daily company-provided lunches and Thursday socials to monthly potlucks, company events, and volunteer opportunities that have a real impact in the community. Compensation: The starting base pay for this role is between $30-$40/hr. The actual base pay is dependent upon many factors, such as training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits, and 401(k) with matching. Jupiter Endovascular provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

🏢 Summary: Quality Control Specialist role in a medical device manufacturing environment focused on receiving, in-process, and final inspections for catheter-based cardiovascular products. The position supports quality systems, nonconforming product reviews, equipment calibration, environmental monitoring, and lot release activities in an in-office setting. Offers competitive compensation, equity opportunities, comprehensive benefits, and professional growth in a fast-paced startup environment. 🗂️ Requirements: High school diploma or equivalent, Minimum 2 years of hands-on quality inspection experience in medical device manufacturing, Proficiency with word processing software, Proficiency with spreadsheet software, Full professional proficiency in English, Ability to perform receiving, in-process, and final inspections, Experience documenting nonconforming products, Ability to maintain traceability records and quality system documentation 📃 Skills: QC, Inspection, Calibration, Monitoring, NCR, NCMR, CAPA, Traceability, Sampling, Microscopy, Excel, Word 🏢 Description: Company Summary: Join a team that's redefining what's possible in cardiovascular treatment. At Jupiter Endovascular, we're revolutionizing catheter-based therapies by bringing the precision and control of surgery to minimally invasive procedures. For decades, catheters have remained largely unchanged—rigid, unstable, and difficult to maneuver through the body's winding anatomy. We've developed a transforming fixation technology that navigates flexibly through the vascular system, then locks into place to deliver treatment with surgical-like stability and control. Our device solves one of the longest-standing challenges in endovascular procedures, empowering physicians and improving outcomes for millions of patients living with cardiovascular disease. We're entering an exciting new phase—scaling up production, expanding our team, and preparing for commercial launch. Founded and headquartered in Menlo Park, California, Jupiter Endovascular is led by a proven team of medical device entrepreneurs and backed by top-tier investors across venture capital, private equity, and strategic partners. We've built a fast-paced, collaborative culture grounded in innovation, teamwork, and purpose. Every role at Jupiter directly contributes to our mission: saving lives by advancing the future of endovascular therapy. Position Overview: The Quality Control Specialist is primarily responsible for receiving, in-process, and final product inspections. The QC Specialist may also perform equipment calibration and maintenance coordination and environmental monitoring activities in accordance with established quality system procedures. This role also supports nonconforming product disposition, traceability, lot release, and other quality assurance activities as assigned. This is an in-office role. Responsibilities: - Perform product receiving, in-process, and final inspections in accordance with written procedures, statistical sampling plans, engineering drawings, and product specifications, documenting nonconforming products as appropriate. - May administer the equipment calibration and maintenance system, environmental monitoring program, and bioburden monitoring program, including coordination with subcontracted service providers. - Coordinate or lead nonconforming product reviews, including Material Review Board activities and NCR/NCMR disposition, to support timely product decisions. - Maintain quality system logs, records, and filing systems, and ensure accurate traceability of components and finished products. - Maintain and operate inspection and test equipment, and provide input on inspection methods and quality procedures. - Support corrective and preventive action activities, supplier evaluations, and supplier performance monitoring. - Review product lot history records and support lot release to finished goods inventory, as applicable. - Support finished goods shipping and commercial release activities, as applicable. - Contribute to improvements in quality system procedures and work instructions related to areas of responsibility. - Train and advise other employees on quality-related requirements and ensure effective communication across functions. - Represent areas of responsibility during internal and external quality audits and support audit readiness. Qualifications: - High school diploma or equivalent required. - Minimum of two years of experience with hands on quality inspection in a medical device manufacturing environment required. - Startup or small-company experience preferred. - Catheter manufacturing experience preferred. - Proficiency with word processing and spreadsheet software required. - Full professional proficiency in English required. Preferred Qualifications: - Experience reading and interpreting engineering drawings, specifications, and statistical sampling plans. - Experience using dimensional and visual inspection equipment, including microscopes. - Strong hand-eye coordination, manual dexterity, color vision, and visual acuity, corrected if necessary. - Ability to work under pressure, manage multiple deadlines, and maintain effective working relationships. - Strong attention to detail, organizational skills, and oral and written communication skills. Why Jupiter Endovascular? - Work in a culture built on shared purpose, where passionate teammates support one another and stay motivated by improving patient lives. - Thrive in a collaborative environment that values new ideas, gives everyone a voice, and offers professional growth and exposure across departments as the company enters an exciting phase of expansion. - Earn competitive pay with performance incentives and equity opportunities. - Enjoy comprehensive, top of the market medical, dental, and vision coverage focused on meaningful premium support and smart savings. - Access meaningful benefits including a top tier 401(k) with a best in-class plan design which includes strong employer contributions, short and long-term disability, life insurance, commuter benefits, and wellness support. - Take advantage of a healthy paid time off policy, company holidays, and an environment that encourages a healthy work-life balance. - Strengthen relationships through shared experiences - from daily company-provided lunches and Thursday socials to monthly potlucks, company events, and volunteer opportunities that have a real impact in the community. Compensation: The starting base pay for this role is between $30-$40/hr. The actual base pay is dependent upon many factors, such as training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits, and 401(k) with matching. Jupiter Endovascular provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

🏢 Summary: The offer is for a Quality Systems Specialist role focused on developing and maintaining a Healthcare Quality Management System for medical software products classified as Software as a Medical Device. The position involves ensuring regulatory compliance for EU and US markets, supporting audits, documentation, and quality processes across the full software lifecycle. The role emphasizes continuous improvement and alignment with medical device standards. 🗂️ Requirements: Minimum 3 years experience with medical device quality systems, Practical experience with ISO 13485, Practical experience with ISO 14971, Degree in engineering, medical technology, life sciences or related field, Experience with structured documentation in regulated environments, Ability to coordinate with multiple stakeholders, Strong analytical and documentation skills, Professional proficiency in English 📃 Skills: ISO13485, ISO14971, IEC62304, Agile, QMS, Audit, RegulatoryCompliance, Documentation, Validation 🏢 Description: Project overview You will be involved in the development and maintenance of a Healthcare Quality Management System that supports multiple medical software products delivered to international markets. The project focuses on aligning software engineering practices with medical device regulations and quality standards. Position overview We are looking for a Quality Systems Specialist who will contribute to building and maintaining quality systems for medical software products classified as Software as a Medical Device. You will work on regulatory compliant digital health solutions intended for the EU and US markets, focusing on quality processes, documentation, audits, and continuous improvement across the full software lifecycle. Responsibilities Maintain and support the Healthcare Quality Management System and its ongoing certification activities. Support preparation for and participation in external audits, including evidence collection and audit coordination. Provide quality support to medical software projects throughout planning, development, release, and maintenance phases. Prepare and execute internal audits, including audit planning, documentation, reporting, and follow up actions. Support coordination and tracking of corrective and preventive actions. Collaborate with engineering, legal, compliance, and other internal teams on quality and regulatory topics. Participate in customer audits and supplier evaluations within the scope of assigned projects. Contribute to continuous improvement initiatives and systemic quality enhancements. Support validation activities for quality management and documentation tools. Promote quality awareness by delivering internal workshops and training sessions. Requirements At least three years of experience working with medical device quality systems. Practical experience with ISO 13485 and ISO 14971. A degree in engineering, medical technology, life sciences, or a comparable field. Experience working with structured documentation and regulated processes. Ability to work independently while coordinating effectively with multiple stakeholders. Strong analytical, documentation, and written communication skills. Professional working proficiency in English. Interest in developing skills in regulatory affairs for medical software. Nice to have Experience participating in or conducting audits. Exposure to IEC 62304 or other medical software lifecycle standards. Understanding of Agile software development practices. Initial experience with EU or US medical device regulatory frameworks. What We Offer: Vacation days : Up to 26 business days per year. 10 illness/special days off per year (fully paid, no medical papers needed) for all contract types Health and life insurance (Luxmed) MyBenefit platform with Multisport option Internal psychological support service English language classes from the first working day Access to external learning platforms : O’Reilly, LinkedIn Learning, Udemy, and a wide catalog of diverse internal training Flexible workplace : work from the office, from home, or choose a hybrid option Tech Skills Mentoring Program Opportunities to develop as a public speaker, mentor, or technical interviewer Fully paid idle (bench) when not involved in a project Certification reimbursement (AWS, GCP, Microsoft, etc.)

🏢 Summary: Entry-level Associate Quality Assurance Analyst role within an engineering team, focused on ensuring software quality through manual testing, test planning, and defect management in an Agile environment. The position involves collaborating with product managers and scrum teams to validate features, APIs, and user experiences across browsers and devices. The role also includes root-cause analysis, backlog management, and supporting continuous delivery processes. 🗂️ Requirements: Bachelor’s degree in Computer Science, Software Engineering, or equivalent experience, Understanding of quality assurance techniques, Knowledge of testing approaches in Scrum Agile environments, Understanding of functional, regression, negative, system, API, and user acceptance testing, Ability to create test plans and test cases from business requirements, Ability to investigate issues using logs and developer tools, General SQL proficiency, Authorization to work in the U.S. 📃 Skills: QA, Testing, ManualTesting, APITesting, RegressionTesting, SQL, Scrum, Agile, SmokeTesting, SystemTesting, UserAcceptanceTesting 🏢 Description: Total Expert is the Customer Operating System for financial services. Our Customer for Life Platform combines a system of context with a system of action that enables humans and AI Agents to engage in the moments that matter and earn customers for life. Since 2016 Total Expert has enabled more than seven trillion dollars of funded loan volume. We are looking for an Associate Quality Assurance Analyst to join our growing engineering team. The major accountability of this position involves being a key member of the development team ensuring quality assurance of software deliverables within release schedules through the writing of test conditions/cases, test plans, and the utilization of test and reporting tools. This position will work directly with product managers to understand product concept, release goals and critical user flows. Responsibility includes prompt communication of defects and problems, project status, as well as concerns and issues to scrum teams and manager. What you’ll be doing: - Learning the Total Expert platform and quality assurance best practices - Assist in test planning and estimations - Create and execute manual test cases - Create and review test plans and test cases - Reproduce and clearly document all issues found during verification and validation - Clearly document validation and verification results - Maintain and review defect backlog and assist in prioritization of efforts - Conduct root-cause analysis for critical defects released to our customers or as needed to improve processes - Understanding the user experience and the ability to fully test its quality across multiple browsers and devices - Work with the team to plan, develop, and execute software tests that cover smoke testing, feature testing, API testing, and post-release validation - Investigate issues using server logs, browser developer tools, and other resources and tools available What we are looking for: - Bachelor’s degree in Computer Science, Software Engineering, or equivalent work experience - General understanding of quality assurance techniques with the ability to apply - General understanding of testing approaches within Scrum agile software development environment - General understanding of functional, regression, negative, system level, API and user acceptance testing - General ability of how to break work down into small pieces in a continuous delivery environment - General ability to turn business requirements into test plan/cases - Able to explain technical problems to non-technical people - General understanding of SQL proficiency - Passionate about testing - Must have an innovative outlook and a desire to seek new and more effective ways of testing - Ability to work and produce consistent results independently and in group settings Compensation/Benefits: The anticipated base salary range for this role is $60,000 - $70,000 annually. Final total compensation offered is dependent upon the selected individual's qualifications and experience. This position is also eligible for an annual discretionary bonus based on company performance and other factors. As an employee, you will be eligible to participate in the Employee Stock Option Plan. The company offers a competitive range of benefits including Medical, Dental, Vision, HSA (Health Savings Account), FSA (Flexible Spending Accounts), company paid Life Insurance, Short-Term Disability, Long-Term Disability, Flexible Time-Off (FTO), Paid Parental Leave, and 401(k) with employer match. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

🏢 Summary: The role involves testing web and mobile healthcare applications to ensure quality, performance, and compliance with business and design requirements. You will conduct various types of testing, report and analyze bugs, and collaborate closely with developers and stakeholders throughout the product lifecycle. The position requires ownership of the testing process and strong technical problem-solving skills in an agile environment. 🗂️ Requirements: 3+ years of experience as a Quality Assurance Specialist, Experience testing web applications, Experience testing mobile applications, Understanding of REST API and HTTP methods, Experience with bug reporting and tracking, Knowledge of testing methodologies, Experience working in Agile environment, Ability to analyze error codes and identify root causes, Proficiency in English (B2), Proficiency in Polish (B2) 📃 Skills: REST, HTTP, JIRA, Postman, JMeter, Browserstack, Charles, ADB, Logcat, DevTools, AndroidStudio, Agile, Git 🏢 Description: Got a nose for detail? Looking for a new challenge? We are currently on the search for a Quality Assurance Specialist. Join our team! About Momentum: At Momentum, we accelerate digital innovation in healthcare. Our mission is to empower HealthTech startups and scaleups by transforming ideas into cutting-edge digital products. We combine deep industry expertise, strategic consulting, and full-stack development to create solutions that drive growth, compliance, and patient impact. We believe in technology that makes healthcare more accessible, efficient, and human-centered. Requirements: 3+ years of experience as a Quality Assurance Specialist Experience testing Web and Mobile applications Familiarity with REST api, understanding the structure of HTTP requests and the methods used in client-server communication Bug reporting and advocacy Familiarity with test tools as: Browser DevTools, android studio (ADB, Logcat), Postman (REST API), Charles, JMeter, Browserstack, JIRA Knowledge of testing methodologies, agile development and product lifecycle Note-taking Analyzing common error codes and being able to identify the cause of problems Good English, both written and spoken (B2) Good Polish, both written and spoken (B2) Ethics and self-management Ownership of the testing process Technical problem solving Nice to have: Coding skills Git knowledge Familiarity with context driven testing Responsibilities: Web and mobile application testing Verifying app against design and business requirements Functional, exploratory, smoke, ad-hoc and regression testing Reporting bugs and issues in JIRA Keeping test documentation up to date Participating in client meetings and conducting product demos Collaborating closely with both the development and other QAs to enhance the quality and performance of existing and future projects What We Value: Clarity in focus and dedication to building digital products that elevate healthcare and improve quality of life. Flair to face challenges with boldness, creativity, and a proactive mindset. Grit to take ownership, stay ambitious, and deliver refined, high-quality solutions. Impact through meaningful innovation that makes pioneering medical discoveries accessible and human-centered. Ability to collaborate efficiently in teams of technical and non-technical individuals, and comfortable working in a dynamic environment with evolving objectives and iteration with users. What we offer: Modern Workspace: We provide a modern and comfortable office environment, right in the heart of Wrocław. Work-Life Harmony: Enjoy flexible working hours, allowing you to find the perfect balance between work and life. Stay Active: Our company Multisport benefit encourages you to stay fit and take care of your well-being. Your Health Matters: Access to private healthcare ensures you're taken care of when you need it most. Remote Support: For our remote team members we offer reimbursement for necessary and the non-necessary office visits. Freedom of choice: We understand that we all have different lifestyles and needs, that's why the Worksmile Cafeteria System gives you access to hundreds of non-wage benefits to choose from. Security and peace of mind: We provide the option to join our comprehensive insurance plan, for your and your loved one’s security. Team Building & Development Fun(d): We believe in the power of fun and development, and microfunds are here to bring some excitement into your work-life or you can access them to develop your skills and gain knowledge. Thinking of applying? Awesome! Here’s what happens next: As a standard, we keep our recruitment processes short and to the point. Here is a detailed breakdown of the workflow for this position: Initial phone interview (20 min) : We'll have a quick chat to get to know each other and discuss your experience. It's a great opportunity for us both to see if there's a good fit. Recruitment task : Following the interview, we will send you a short task to complete. You will have three working days to complete and return it. Technical interview (45-60 min) : If your task is successful, you'll be invited to a technical interview. You will meet with a senior team member to dive deeper into your technical knowledge and discuss your solution. Culture fit meeting (20-30 min) : Next, you'll have a relaxed chat with our IT Team Manager and a recruiter. We'll talk about our company values and see if your working style aligns with ours. Work reference : After that, we'll ask you to share a work reference. Decision and feedback : After all the stages are complete, we'll get back to you with our final decision and detailed feedback on your application. If you have any questions, get in touch with us!

🏢 Summary: Senior/Expert Quality Assurance Engineer role focused on building and maintaining automated testing frameworks, improving QA practices, and integrating testing into CI/CD pipelines within an agile engineering environment. The position involves collaborating with cross-functional teams to ensure high-quality product delivery, mentoring teams on quality standards, and supporting modern software architectures and testing methodologies. 🗂️ Requirements: 6+ years of experience in manual and automated software testing, Knowledge of software testing theory, Experience developing and maintaining test automation frameworks, Strong experience with testing practices across unit, load, endurance, and cross-platform testing, Experience with CI/CD pipelines and monitoring tools, Knowledge of Kubernetes and Docker, Experience with UI testing, REST protocols, and microservice architecture, Experience with mobile QA engineering tools and frameworks, Strong programming skills in Java/Kotlin and Swift, Experience working in Agile Scrum environments, Ability to work autonomously and self-organize, English communication skills 📃 Skills: Java, Kotlin, Swift, Jenkins, Kibana, Grafana, Kubernetes, Docker, Espresso, XCUITest, TestRail, Bitrise, Postman, RestAssured, BrowserStack, REST, CI/CD, Scrum, Bitbucket, CharlesProxy 🏢 Description: Company Description With over 25 years’ experience, plus the same enormous passion and ambition we had on day-one, we’re trailblazers in the pet e-commerce industry. Our solutions make over 12 million customers genuinely happier – and that’s something we really care about. We work together to continually adapt; embracing change and the challenges it brings so that we can keep doing better. Join us and discover a place where your potential meets your passion for pets. That’s the power of plus. Job Description We seek an Expert Quality Assurance Engineer to join our SHOPPING department within the Engineering and operation function zooplus, bring new features to life, and support our products' move to modern agile and technical practices and architectures. As a seasoned Quality Assurance Engineer specializing in automation and cutting-edge software testing methodologies, you play a pivotal role in upholding the highest quality standards within your team. Reporting directly to the Engineering Manager, you spearhead the quality assurance efforts, ensuring seamless collaboration across various functional teams. You serve as the beacon of excellence in product delivery and deployment, setting the benchmark for quality standards. Your expertise serves as a bridge to the QA Center of Practice, facilitating the exchange of best practices within and beyond your team. Your primary objective is cultivating a culture of excellence and efficiency in quality assurance, freeing up valuable time for your team to focus on innovative solutions rather than redundant testing procedures. By leveraging advanced tooling and coding techniques, you seamlessly integrate automation testing into every team member's daily workflow. Through close collaboration with cross-functional teams, you drive the implementation of new features and enhancements, ultimately enhancing the experience for over 9 million customers. As our Expert Quality Assurance Engineer, you embrace the following responsibilities : Take ownership and responsibility for the design and development of all aspects of testing. Work on acceptance criteria and test scenarios with the Product Owner and development team. Design, execute, and maintain test scenarios and automation capabilities for all test levels and types (e.g., automated, regression, exploratory, etc.). Create and optimize test frameworks and integrate them into deployment pipelines. Participate in the code review process for both production and test code to ensure all critical cases are covered. Monitoring test runs, application errors and performance. Making information flow, keeping the team informed and being a stakeholder in releases and defect tracking. Share the best testing and quality practices and processes across Zooplus. Promote and coach the team towards a quality-focused mindset. Influence and lead the team towards continuous improvement and best testing practices. Be the reference of the QA Center of Practice , promoting their practices and influencing their strategy, bringing your team experience into their plan. Qualifications As a Senior/Expert Quality Assurance Engineer, you must be able to provide among these: Knowledge of software testing theory. Comfortable in developing test automation frameworks from scratch and maintaining existing frameworks. 6+ years of experience in software testing , manual and automated Strong experience in different testing practices (from unit to load to endurance to cross-platform) specifically integrated within CI/CD. Experience working with CI/CD pipelines and monitoring tools (e.g. Jenkins,, Kibana, Grafana, etc.). Knowledge with K8s, Docker Knowledge of UI testing, REST protocol and microservice architecture Mobile QA Engineering requirements Espresso, XCUITest Testrail Bitrise, Jenkins Charles Proxy Postman and API testing (e.g., Rest Assured) BrowserStack Strong experience in Java/Kotlin, Swift , as well as its usage under a CI/CD pipeline. Ability to work in an agile environment, engaged in Scrum Ability to work in an autonomous, self-responsible and self-organized way. Able to effectively communicate in English . Nice to have: Knowledge with Bitbucket, Experience with AI-assisted development and modern SDLC tooling: Tools like GitHub Copilot / Copilot Chat Applying AI for code generation, refactoring, test automation, and documentation Using AI to accelerate debugging, prototyping, and architectural decisions Additional Information Headquartered in Munich, with offices across Madrid, Krakow, Wroclaw, London and Vienna, we collaborate because we genuinely love working together - so you’ll be at the heart of an incredible, multinational team. We trust each other to get the job done, which means you’ll benefit from hybrid working, spending 60% of your time in the office and 40% at home. There’s an option to work for 20 days abroad in approved countries too. Add to that development opportunities that help you to shape your own career path, excellent training and support, wellbeing offers, subsidised transport or bike leasing, plus 20% discount across all our products, and you’ll begin to get a sense of what sets us apart. Find out more about the specific benefits at your local office in our blog posts . A note on compensation: We believe in being transparent about salary ranges. The range shown reflects the full scope that the role can grow into over time, depending on experience, skills, and impact. Most offers are positioned around the midpoint of the range, ensuring a fair and consistent approach across our teams. At zooplus, we believe in equal opportunity and support everyone to fulfil their potential. We recognise the power of listening and learning from each other and embrace diversity and inclusion of all.

🏢 Summary: The Manager, Quality Systems leads and continuously improves the Quality Management System for a medical device company, ensuring compliance with FDA, ISO 13485, EU MDR, CHAP, and DME requirements. The role oversees document control, CAPA, nonconformance, audits, training, and regulatory activities while serving as deputy management representative during inspections. This position drives audit readiness, regulatory compliance, and cross-functional quality initiatives in a regulated manufacturing environment. 🗂️ Requirements: 5+ years Quality Assurance experience in medical device industry, 2+ years people management experience, Knowledge of ISO 13485, Knowledge of 21 CFR Part 820, Knowledge of FDA Quality System Regulations, Knowledge of EU MDR requirements, Experience in regulated manufacturing environments, Experience with eQMS systems, Experience with PLM systems, Experience managing CAPA and nonconformance processes, Experience conducting internal and external audits, Experience working with regulatory agencies (FDA, BSI, CHAP), Ability to manage DME compliance requirements 📃 Skills: ISO13485, 21CFR820, FDA, EUMDR, eQMS, PLM, CAPA, Audit, Nonconformance, DME, CHAP, BSI 🏢 Description: Element Science, Inc. is a medical device and digital health company redefining how patients with heart disease are monitored and treated as they transition from the hospital to the home. Our mission is to improve outcomes for patients at risk of life-threatening cardiac events through innovative solutions at the intersection of clinical-grade wearables, advanced algorithms, and therapy delivery. We are entering an exciting phase of growth as we move from development into early commercialization. Our approach combines hardware, software, and services to deliver a more personalized and seamless patient experience—designed with both patients and clinicians in mind. Our product, a wearable patch defibrillator, is designed for patients with a temporary elevated risk of sudden cardiac arrest, addressing a significant and underserved population of over 500,000 patients in the U.S. By focusing on comfort, usability, and clinical effectiveness, we aim to transform the standard of care during this critical period. SUMMARY OF ROLE: The Manager, Quality Systems is responsible for day-to-day operation and continuous improvement of the Quality System. The role is responsible for Document Control, Training Program, Change Control, Internal & External Audit Program, Management Review, Nonconformance management and CAPA management. The Manager, Quality Systems serves as deputy management representative representing the organization in internal and external audits. This role serves as co-system administrator for eQMS and works with cross functional stakeholders ensuring the organization continues to maintain CHAP accreditation and compliance with DME requirements including managing external DME audits, maintaining quality documentation and ensuring adherence to regulatory standards. This role supports EU MDR deliverables in collaboration with external regulatory consultants. This role plays a key part in sustaining a compliant, audit-ready QMS that upholds patient safety and organizational integrity. RESPONSIBILITIES: - Lead, mentor, and develop Quality Systems team members, fostering a culture of quality, accountability, collaboration, and continuous improvement - Partner cross-functionally to investigate quality issues, interpret data trends, and drive timely, risk-based decisions - Build and maintain strong working relationships with internal stakeholders, external auditors, and regulatory partners - Own and maintain the Document Control system, ensuring controlled documents remain accurate, current, compliant, and properly version-controlled - Administer and continuously enhance the company training program, ensuring timely completion, training effectiveness, and maintenance of compliant training records - Own the CAPA program, including driving timely resolution of aging CAPAs, ensuring robust root cause investigations, and monitoring closure effectiveness and metrics - Manage Nonconformance (NC) processes from initiation through final disposition and closure, ensuring timely and compliant execution - Lead Management Review activities, including development of quality metrics, trend analysis, and executive-ready Quality Management Review (QMR) materials - Monitor, analyze, and trend quality system metrics to proactively identify systemic risks, drive corrective actions, and support continuous improvement initiatives - Support post-market surveillance activities, including maintenance of associated documentation and reporting requirements - Support EU MDR compliance activities in partnership with external regulatory consultants, including CERs, PSURs, and PMS deliverables - Maintain quality documentation and records necessary to support BSI certification activities and ongoing CE mark compliance - Own and execute the Internal Audit Program, including audit planning, scheduling, execution, findings management, and verification of corrective action closure - Coordinate CHAP accreditation activities and ongoing DME compliance requirements, including preparation for and management of external audits - Partner with external auditors and regulatory agencies to support inspections, audits, and compliance readiness activities - Ensure the Quality Management System remains compliant with FDA, ISO 13485, CHAP, EU MDR, and other applicable regulatory and quality standards - Support system validation activities, process improvements, and ongoing enhancements to quality systems and tools as needed QUALIFICATIONS: - 5+ years of progressive Quality Assurance experience within the medical device industry, including experience in regulated manufacturing environments - 2+ years of people leadership or management experience, with demonstrated ability to lead and develop high-performing teams - Strong working knowledge of ISO 13485, 21 CFR Part 820, FDA Quality System Regulations, and EU MDR requirements - Hands-on experience utilizing eQMS and PLM systems to support quality and compliance initiatives - Ability to interpret, implement, and adapt to evolving regulatory requirements, including DME quality system standards - Solid understanding of core quality processes, including CAPA, nonconformance management, complaint handling, change control, and internal auditing - Experience partnering with external auditors and regulatory agencies, including BSI, FDA, CHAP, or equivalent organizations - Demonstrated ability to manage multiple priorities and drive execution in a fast-paced, evolving environment - Strong analytical and problem-solving skills, with the ability to identify trends, summarize findings, and communicate recommendations to leadership BENEFITS: Element Science offers a very competitive salary and benefits package including, but not limited to: - Stock Options - 90% employer-paid medical, dental, and vision insurance - Company-paid Basic Life Insurance - 401(k) retirement plan (Traditional and Roth) - Competitive Paid Time Off - Paid Holidays - FSA (Flexible Spending Accounts) - HSA (Health Savings Account) - Employee Assistance Program through PEO The salary for this exempt-level position will be based on experience and qualifications within an established pay range. Pay range: $144,000 - $154,000 Element Science is an Equal Opportunity Employer. All candidates will be evaluated on the basis of their qualifications for the job in question. We do not base our employment decision on non-merit-based factors prohibited by law. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. We are not able to sponsor individuals for employment visas for this job. At this time, we are unable to offer relocation assistance.

🏢 Summary: Inventory Specialist role supporting aerospace R&D and manufacturing operations through inventory management, material handling, shipping, and logistics coordination. The position focuses on maintaining accurate material flow, supporting production teams, and improving warehouse efficiency in a fast-paced aerospace environment. Includes competitive compensation, equity, healthcare, retirement benefits, and paid time off. 🗂️ Requirements: 2+ years inventory, logistics, or warehouse experience in manufacturing, aerospace, or defense, Experience with ERP/MRP inventory management systems, Forklift certification or ability to obtain certification, Proficiency with Windows and Microsoft Office, Ability to maintain accurate inventory records, Ability to lift up to 50 lbs, Ability to stand for extended periods, Availability for extended hours or weekends when needed, Commitment to safety, quality, and continuous improvement, Eligibility under U.S. export control regulations 📃 Skills: ERP, MRP, NetSuite, SAP, Windows, Outlook, Word, Excel, Teams, Forklift, ESD, Cleanroom, 5S, Logistics, Inventory, Shipping 🏢 Description: About the Role: As an Inventory Specialist, you will play a critical role in enabling efficient and accurate material flow across R&D and manufacturing operations. You’ll manage all stages of the inventory process—receiving, stocking, tracking, picking, and shipping hardware that directly supports vehicle and propulsion development. This position requires exceptional attention to detail, strong organizational skills, and the ability to thrive in a fast-paced, evolving aerospace environment. Working closely with technicians, engineers, and program teams, you’ll ensure materials are always where they need to be—on time and to spec. Responsibilities - Receive, inspect, and document incoming materials, ensuring accuracy and traceability of all shipments. - Manage material storage and organization by maintaining inventory bins, racks, and labeling systems. - Perform cycle counts, reconciliation, and auditing to maintain inventory accuracy. - Safely operate forklifts, pallet jacks, and other material handling equipment to support warehouse operations. - Pick, package, and ship materials with proper documentation, handling, and export compliance where applicable. - Coordinate material transfers between fabrication, assembly, and test teams to support production flow. - Identify and implement process improvements that enhance safety, accuracy, and efficiency across the inventory lifecycle. Requirements - 2+ years of experience in inventory, logistics, or warehouse operations within manufacturing, aerospace, or defense environments. - Proven ability to work with inventory management systems (ERP/MRP) and maintain accurate records. - Forklift certification or ability to become certified upon hire. - Basic proficiency in Windows and Microsoft Office (Outlook, Word, Excel, Teams). - Strong attention to detail and organizational discipline in a fast-moving production environment. - Capable of lifting up to 50 lbs, standing for long periods, and working extended hours or weekends when needed. - Demonstrated commitment to safety, quality, and continuous improvement. Preferred Skills and Experience - Experience supporting engineering development, R&D, or prototype build programs. - Familiarity with aerospace material handling, including ESD, cleanroom, and hazardous material protocols. - Knowledge of tooling and fixturing logistics for prototype or production builds. - Experience with shipping logistics, import/export compliance, and freight coordination. - Proficiency with inventory management or ERP systems (e.g., NetSuite, SAP, or similar). - Demonstrated success in implementing 5S or lean warehouse practices. - Strong communication skills and ability to interface across engineering, procurement, and production teams. Physical Requirements - Prolonged periods of sitting at a desk and working on a computer. - Frequent walking through office, manufacturing, and test facility environments. Benefits - Health & Wellness: 100% employer-paid healthcare and pet insurance. - Financial: Competitive pay, stock options, 401(k) retirement plan, and potential year-end bonuses. - Time Off: Paid parental leave, 12 federal holidays, unlimited PTO for exempt employees, and generous accrued PTO for non-exempt employees. - Office Perks: Weekly paid office lunches and fully stocked breakrooms. U.S. Export Control Compliance Status The person hired will have access to information and items subject to U.S. export controls and therefore must either be a U.S. person as defined by 22 C.F.R. § 120.62 or otherwise eligible for deemed export licensing. Equal Opportunity Employment decisions are based solely on merit, competence, and qualifications, without regard to legally protected status.

🏢 Summary: The role focuses on ensuring inventory accuracy, material availability, and regulatory compliance across 503A and 503B pharmaceutical operations. It supports manufacturing continuity through inventory control, cycle counting, material movement, and AI-enabled analytics and reporting. The position drives operational efficiency and continuous improvement within a fast-paced, regulated environment. 🗂️ Requirements: High School Diploma or equivalent, Minimum 2 years of inventory control, warehouse operations, materials management, or supply chain experience, Experience with cycle counts, inventory audits, and inventory transactions, Proficiency with ERP systems and inventory management software, Ability to maintain accurate documentation in regulated environments 📃 Skills: ERP, Inventory, Analytics, Automation, Forecasting, Reporting, Compliance, AI, Dashboards 🏢 Description: POSITION SUMMARY Inventory Control Coordinator ensures inventory accuracy, material availability, and compliance across 503A and 503B operations. This role manages inventory transactions, stock reconciliation, cycle counts, material movement, and reporting supporting manufacturing continuity and operational efficiency. Leveraging AI-enabled analytics, automation, forecasting insights, and digital inventory systems, the position improves inventory visibility, decision-making, and execution. RESPONSIBILITIES Inventory Management Inventory Accuracy: Maintains accurate inventory records, reconciliations, and system transactions supporting inventory integrity and manufacturing continuity. Utilizes AI-enabled analytics, inventory platforms, and automated reporting tools to improve stock visibility, strengthen accuracy, and support scalable inventory control execution. Cycle Counting: Performs cycle counts, inventory audits, and stock verification activities ensuring inventory accuracy and compliance. Leverages AI-powered monitoring, variance analysis, and reporting tools to identify discrepancies, improve reconciliation speed, and strengthen inventory accountability. Material Control: Manages material movement, transfers, replenishment activities, and inventory transactions supporting production and warehouse operations. Applies AI-assisted workflow automation and inventory dashboards to improve traceability, visibility, and material flow efficiency. Operational Excellence Stock Monitoring: Monitors inventory levels, usage trends, and material consumption patterns supporting proactive inventory management. Utilizes AI-enabled forecasting and planning tools to identify risks, improve stock availability, and support operational continuity. Process Compliance: Executes inventory activities according to company procedures and regulatory requirements supporting compliance and operational consistency. Leverages AI-powered compliance monitoring and workflow automation tools to improve execution quality and reduce operational risk. Issue Resolution: Identifies inventory discrepancies, transaction errors, and material shortages impacting operations. Applies AI-assisted analytics and root cause investigation techniques to improve resolution speed and strengthen corrective actions. Cross Functional Collaboration Stakeholder Support: Partners with Supply Chain, Manufacturing, Warehouse, Procurement, and Quality teams to support inventory alignment and material availability. Utilizes AI-enabled collaboration tools and operational dashboards to improve communication and issue resolution. Data Reporting: Maintains inventory reports, metrics, and documentation supporting data-driven decision-making. Leverages AI-assisted dashboards and reporting technologies to improve reporting accuracy, visibility, and operational insights. Continuous Improvement: Identifies opportunities to improve inventory workflows, storage practices, and operational efficiency. Applies AI-powered analytics, automation technologies, and continuous improvement methodologies to enhance inventory performance and support enterprise growth. KNOWLEDGE AND SKILLS Strong understanding of inventory control, warehouse operations, stock reconciliation, cycle counting, and material management within regulated environments. Proficiency using ERP systems, inventory management software, AI-enabled inventory analytics tools, and reporting platforms. Demonstrated ability to identify inventory discrepancies, resolve operational issues, and maintain accurate documentation. Excellent organizational, communication, and problem-solving skills with the ability to manage multiple priorities effectively. EXPERIENCE AND QUALIFICATIONS High School Diploma or equivalent required; Associate degree preferred. Minimum 2 years of inventory control, warehouse operations, materials management, or supply chain experience preferred. Experience performing cycle counts, inventory audits, inventory transactions, and inventory reporting strongly preferred. Familiarity with ERP systems, inventory management software, and regulated operational environments preferred. Demonstrated ability to execute accurately, adapt quickly, and contribute effectively within fast-paced teams. Employee Benefits, Health and Wellness: We offer comprehensive benefits to support your health, well-being, and future, including medical, dental, and vision coverage, paid time off, 401(k) matching, wellness perks, IV therapy, and compounded medications. Physical Requirements: While performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. Employees are regularly required to move about the office and around the corporate campus. The employee is regularly required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.

🏢 Summary: The Inventory Control Coordinator ensures inventory accuracy, material availability, and regulatory compliance across 503A and 503B pharmaceutical operations. The role focuses on managing inventory transactions, cycle counts, material movement, and reporting while leveraging AI-enabled analytics and digital inventory systems to improve visibility and operational efficiency. This position supports manufacturing continuity in a fast-paced, regulated environment through disciplined inventory management and data-driven decision-making. 🗂️ Requirements: High School Diploma or equivalent, Minimum 2 years of inventory control, warehouse operations, materials management, or supply chain experience, Experience performing cycle counts, inventory audits, and inventory transactions, Proficiency with ERP systems and inventory management software, Ability to maintain accurate inventory records and documentation in regulated environments 📃 Skills: ERP, Inventory, Analytics, AI, Automation, Forecasting, Reporting, Dashboards, Compliance, Warehouse 🏢 Description: Empower Pharmacy is a visionary healthcare company dedicated to making quality, affordable medication accessible to millions of patients nationwide. As the nation's most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility, we're redefining what's possible in personalized medicine and pharmaceutical manufacturing. We're proud to be recognized as one of Houston's fastest-growing private companies and ranked #116 in Healthcare & Medical on the Inc. 5000 List for 2025. Our strength is built on four core values: People, Quality, Service, and Innovation. Guided by these principles, we've created a uniquely integrated healthcare platform powered by advanced technology, operational excellence, and a relentless commitment to patient care. From manufacturing and quality control to distribution and customer experience, our teams work together to raise industry standards, expand access to critical medications, and improve outcomes for patients and providers across the country. At Empower, joining our team means more than starting a new role. It means becoming part of a mission-driven organization that's transforming healthcare at scale. We invest deeply in our people, encourage bold thinking, and create opportunities for growth, leadership, and innovation at every level. Your ideas matter here, your development is supported, and the work you do has a direct impact on the lives of millions. If you thrive in a fast-moving, purpose-driven environment where innovation, collaboration, and ambition come together, Empower Pharmacy is the place for you. Let's transform healthcare together.POSITION SUMMARY Inventory Control Coordinator ensures inventory accuracy, material availability, and compliance across Empower's 503A and 503B operations. This role manages inventory transactions, stock reconciliation, cycle counts, material movement, and reporting supporting manufacturing continuity and operational efficiency. Leveraging AI-enabled analytics, automation, forecasting insights, and digital inventory systems, the position improves inventory visibility, decision-making, and execution. Success requires execution rigor, learning agility, proactive problem solving, and disciplined inventory management within a hyper-growth, regulated environment. Talent demonstrates accountability, attention to detail, collaboration, and continuous improvement supporting inventory reliability, operational scalability, and business performance. RESPONSIBILITIES Inventory Management Inventory Accuracy: Maintains accurate inventory records, reconciliations, and system transactions supporting inventory integrity and manufacturing continuity. Utilizes AI-enabled analytics, inventory platforms, and automated reporting tools to improve stock visibility, strengthen accuracy, and support scalable inventory control execution. Cycle Counting: Performs cycle counts, inventory audits, and stock verification activities ensuring inventory accuracy and compliance. Leverages AI-powered monitoring, variance analysis, and reporting tools to identify discrepancies, improve reconciliation speed, and strengthen inventory accountability. Material Control: Manages material movement, transfers, replenishment activities, and inventory transactions supporting production and warehouse operations. Applies AI-assisted workflow automation and inventory dashboards to improve traceability, visibility, and material flow efficiency. Operational Excellence Stock Monitoring: Monitors inventory levels, usage trends, and material consumption patterns supporting proactive inventory management. Utilizes AI-enabled forecasting and planning tools to identify risks, improve stock availability, and support operational continuity. Process Compliance: Executes inventory activities according to company procedures and regulatory requirements supporting compliance and operational consistency. Leverages AI-powered compliance monitoring and workflow automation tools to improve execution quality and reduce operational risk. Issue Resolution: Identifies inventory discrepancies, transaction errors, and material shortages impacting operations. Applies AI-assisted analytics and root cause investigation techniques to improve resolution speed and strengthen corrective actions. Cross Functional Collaboration Stakeholder Support: Partners with Supply Chain, Manufacturing, Warehouse, Procurement, and Quality teams to support inventory alignment and material availability. Utilizes AI-enabled collaboration tools and operational dashboards to improve communication and issue resolution. Data Reporting: Maintains inventory reports, metrics, and documentation supporting data-driven decision-making. Leverages AI-assisted dashboards and reporting technologies to improve reporting accuracy, visibility, and operational insights. Continuous Improvement: Identifies opportunities to improve inventory workflows, storage practices, and operational efficiency. Applies AI-powered analytics, automation technologies, and continuous improvement methodologies to enhance inventory performance and support enterprise growth. KNOWLEDGE AND SKILLS Strong understanding of inventory control, warehouse operations, stock reconciliation, cycle counting, and material management within regulated environments. Proficiency using ERP systems, inventory management software, AI-enabled inventory analytics tools, and reporting platforms. Demonstrated ability to identify inventory discrepancies, resolve operational issues, and maintain accurate documentation. Excellent organizational, communication, and problem-solving skills with the ability to manage multiple priorities effectively. EXPERIENCE AND QUALIFICATIONS High School Diploma or equivalent required; Associate degree preferred. Minimum 2 years of inventory control, warehouse operations, materials management, or supply chain experience preferred. Experience performing cycle counts, inventory audits, inventory transactions, and inventory reporting strongly preferred. Familiarity with ERP systems, inventory management software, and regulated operational environments preferred. Demonstrated ability to execute accurately, adapt quickly, and contribute effectively within fast-paced teams. Key Competencies: Customer Focus: Builds trust through customer-centric solutions. Strategic AI: Guides responsible AI adoption and adaptation. Optimizes Work Processes: Drives efficiency with continuous improvement. Collaborates: Partners effectively to achieve shared goals. Resourcefulness: Secures and deploys resources efficiently. Manages Complexity: Simplifies and solves complex challenges. Ensures Accountability: Delivers on commitments with integrity. Situational Adaptability: Adjusts approach to shifting conditions. Communicates Effectively: Tailors messages to diverse audiences. Values: People: Empowering people defines who we are. Quality: Excellence in every product, every time. Service: Serving others is our highest purpose. Innovation: Advancing care through technology and discovery. Employee Benefits, Health and Wellness: We offer comprehensive benefits to support your health, well-being, and future, including medical, dental, and vision coverage, paid time off, 401(k) matching, wellness perks, IV therapy, and compounded medications. Learn more: https://careers.empowerpharmacy.com/benefits/ Physical Requirements: While performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. Employees are regularly required to move about the office and around the corporate campus. The employee is regularly required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.