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Job DescriptionEmbedded Software Engineer (Sr. or Principal Level) Job Status: Full Time Exempt Reports To: Head of Software Engineering Amount of Travel Required: Up to 10% Location: Dallas, TXWork Schedule: Full-timePositions Supervised: None Osteal Therapeutics:Osteal Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing a novel pipeline of combination therapies for orthopedic infections and their consequences. Our lead investigational candidate, VT-X7 was granted Orphan Drug, FastTrack and Qualified Infectious Disease Product designations by the FDA and is currently in late-stage clinical trials for the treatment of Periprosthetic Joint Infection (PJI). With a robust pipeline of additional indications and therapeutic candidates, we anticipate rapid and sustained growth. Position Summary:We are seeking a hands-on Embedded Software Engineer, at a Senior or Principal Level to lead the architecture, development, and verification of safety‑critical firmware for our next‑generation drug‑delivery devices. Your primary responsibility will be embedded software: designing real‑time C/C++ code for microcontrollers (e.g., STM32), ensuring compliance with IEC 62304, and driving software quality through rigorous testing and documentation. You will work closely with electrical, mechanical, and systems teams. The ideal candidate possesses deep embedded software expertise, a passion for medical device innovation, and the ability to mentor others while delivering high‑quality code in a regulated environment. Essential Functions:Essential functions of the position include but are not limited to the following. Other duties may be assigned. · Architect, design, and implement embedded firmware in C/C++ for Class II/III medical devices.· Develop and test analog and digital circuits, including power management, sensors, actuators, and communications interfaces.· Design real‑time software using bare‑metal, state‑machine, or RTOS (e.g., FreeRTOS) paradigms, including bootloaders, low‑level drivers, control loops, and communication protocols (USB, BLE, CAN, Ethernet).· Generate and maintain software design documentation—requirements, architecture, risk controls, and traceability—in accordance with IEC 62304 and FDA 21 CFR 820 design controls.· Plan and execute unit, integration, and system‑level software verification & validation, including automated test frameworks and hardware‑in‑the‑loop setups.· Lead code reviews, static/dynamic analysis, and continuous integration pipelines to enforce coding standards, defensive programming, and regression testing.· Participate in software risk management (software FMEA, cybersecurity analysis) and implement mitigation strategies.· Collaborate with hardware and systems teams on board bring‑up, driver integration, and providing firmware expertise.· Support internal and external audits by presenting software lifecycle evidence and maintaining complete, current design history files.· Mentor junior engineers and champion a culture of quality, continuous improvement, and knowledge sharing.· Stay abreast of emerging embedded software techniques, medical device regulations, and cybersecurity guidance. Position Qualifications:Experience and Education· Bachelor’s or Master’s degree in Computer Engineering, Electrical Engineering, Biomedical Engineering, Computer Science, or a related discipline.· Senior level: 7+ years; Principal level: 10+ years of embedded software development for safety‑critical or regulated products, with demonstrated ownership of full software lifecycle deliverables.· Expertise in C/C++ programming for ARM Cortex‑M or similar MCUs, including low‑level driver development and optimization for power, memory, and performance.· Hands‑on experience with RTOS integration, interrupt‑driven design, and timing‑critical control algorithms.· Proven track record generating software documentation and V&V evidence compliant with IEC 62304, ISO 14971, and FDA QSR.· Proficiency with version control (Git), issue tracking (JIRA), and CI/CD tools (GitHub Actions, Jenkins).· Experience with unit‑test frameworks (Ceedling/Unity, CMock, CppUTest) and static analysis tools (Coverity, C‑STAT, PC‑lint, or equivalent).· Strong problem‑solving skills, including use of oscilloscopes, logic analyzers, and debuggers (JTAG/SWD) to troubleshoot firmware‑hardware interactions. Skills and Abilities· Clear and concise communicator capable of conveying complex technical concepts to cross‑functional teams and executives.· Organized, detail‑oriented, and able to balance multiple priorities in a fast‑paced R&D environment.· Proactive mentor who fosters a culture of excellence, continuous learning, and constructive feedback.· Self‑directed, hands‑on engineer who thrives on delivering reliable products that improve patient outcomes. Computer Software / Programs· Languages: C, C++, Python or Bash scripting for tooling· IDEs/Toolchains: STM32CubeIDE, Keil MDK, IAR EWARM, SEGGER Embedded Studio, GNU Arm· RTOS & Middleware: FreeRTOS, ThreadX, Zephyr, lwIP, USB Device/Host stacks· DevOps & QA: Git, GitHub Enterprise, GitLab, Jenkins, Coverity· Test Automation: Unity, CMock, Pytest, TestStand and Labview The Embedded Software Engineer will play a pivotal role in delivering reliable, safe, and efficient firmware that advances our drug‑delivery platforms while meeting the highest standards of quality and regulatory compliance. If you are passionate about embedded software and driven to improve patient outcomes, we invite you to apply and join our mission to reduce the burden of musculoskeletal infections.

Job Description JOB TITLE: MAINTENANCE AND FACILITIES MANAGER LOCATION: BAUMANN SPRINGS USA GENERAL DESCRIPTION: Maintenance and Facilities Manager will oversee all maintenance aspects of production equipment, facilities and utilities including capital projects and expansions. Co-develop and implement the maintenance strategy and direct their team to maintenance excellence. Work with their team to support project management and product development. Inspire and motivate their staff to achieve new levels and mentor them as they develop new skills and abilities. Strives to improve efficiency and sustainability of processes and product designs, and to reduce waste. Passionate about technology and will report on technical topics to a wide audience. Work autonomously and responsibly by observing all environmental, health and safety (EHS) regulations. Ensure the equipment and building infrastructure is in the best possible condition for a safe, reliable, and efficient operation. AUTHORITY: * Stop any production related activity whose quality or safety is at risk. * Request parts needed for equipment maintenance. * Change maintenance plans as business requires. * Request service for repair of production related equipment * Request for need overtime; or other special personnel changes (i.e., shift change) * Proposal for compensation review and/or matters of disciplinary action * Employee performance reviews (goal setting/mid-year/end-of year) JOB RESPONSIBILITIES (Include but are not limited to): * Plan and execute building maintenance and operational programs * Manage, handle, and supervise maintenance personnel * Management and organization of maintenance staff regarding general company policies, procedures, and practices (on-time, proper dress, interaction, safety, etc.), * Manage and handle all vendor contracts, including vendors for various maintenance items, activities, and tasks. * Ensure the efficiency and operational capacity of building systems * Prepare operation reports, maintenance budgets, and provide analysis of reports to higher-ups * Manage/Coordinate Capital projects including but not limited to facilities, equipment, plant expansions, utilities, etc. * Coordinate with other department heads to make sure all maintenance processes are on track * Develop relationships with building contractors and third- party workers to ensure smooth operations * Develop various facilities/equipment maintenance schedules while managing/resolving maintenance issues. * Manage security systems for the facilities. Ensure maintenance services are provided. * Proposal of metrics and subsequent monitoring of the agree upon targets * Preparation and presentation of projects plans with priorities (i.e., status, actions, etc.) * Provide process-specific information and support to Production Manager for development and achievement of annual Business Plan and Budgeting * Optimize resources through analysis and reporting (equipment and personnel) * Create and provide a safe environment and operation of equipment and processes * Sense of urgency on critical customer equipment repairs * Analyzes malfunctions on a variety of equipment; installs, maintains, repairs or modifies such systems. * Responsible for contacting necessary personnel to obtain information pertaining to difficulties being encountered in the operation of industrial equipment * Analyzes the reported malfunction to determine whether the difficulty is originating in the control systems or is of a mechanical nature by referencing schematics, wire diagrams, manuals, etc. in order to determine most likely cause of malfunction * Analyzes malfunctions; plans and directs the modification, repairing and maintenance of automatic control instruments and related devices used in the operation of industrial manufacturing equipment, AC units and heating systems. * Frequently interacts with internal and external customers, normally involving matters between functional areas, or customers as it relates to maintenance, mechanical or electrical issues. * Provide technical guidance for all aspects related to equipment, facilities, utilities and investments. * Assists with various projects as assigned KNOWLEDGE, SKILLS and ABILITIES: * 4 Year Degree in Mechanical Engineering is preferred * 10-12 years proven work experience as a manufacturing engineer or as an industrial manufacturing professional * 10 years in a technical field in electronics/electro-mechanical related field is desired * 5 years proven experience managing staff and assigning tasks to maintenance technician personnel * Excellent leadership, interpersonal and organizational skills * Ability to communicate effectively with all levels of the organization * Proficient in MS Office and ERP application (SAP) * Motivator, strong messenger of the company’s policies and values * Preferably, background working in the mechanical field. * Excellent process and application knowledge, interpersonal and organizational skills. * Preferably, knowledge of production requirements within the medical device industry * Excellent English language skills (spoken and written) * Exceptional and open communication skills with the ability to work in a global team environment as well as independently. * Good verbal and written communication skills are required * Knowledge and experience working with single phase and 3 phase power systems (11ovac/480ovac). * Exposure to statistical techniques for monitoring machine uptime/downtime trends * Awareness of basic continual improvement philosophies such as Six Sigma, Lean manufacturing, and similar programs. * Experience in PM’s (preventative maintenance) and out-of-specification reporting required. * Troubleshoot/repair of digital controllers and electromechanical production equipment required. * Ability to work independently and troubleshoot issues to determine appropriate course of action. * Must have flexibility to work any shift, and/ or weekends based on business needs * Writing technical reports are a job expectation. * Ability and willing to support between sites as needed Company DescriptionThe BAUMANN Group has been a symbol of Swiss precision and quality for more than 130 years. We invite you to benefit from our experience as one of the world's leading manufacturers of springs and stampings. The group has eleven production sites around the globe, where more than 1,600 people design and produce technically sophisticated products for selected industries, including the automotive, electrical engineering and medical technology sectors. Learn more about BAUMANN visiting our homepage: At Baumann Group, we celebrate diversity and are committed to creating an inclusive environment for all employees. We are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.The BAUMANN Group has been a symbol of Swiss precision and quality for more than 130 years. We invite you to benefit from our experience as one of the world's leading manufacturers of springs and stampings. The group has eleven production sites around the globe, where more than 1,600 people design and produce technically sophisticated products for selected industries, including the automotive, electrical engineering and medical technology sectors. Learn more about BAUMANN visiting our homepage: Baumann Group, we celebrate diversity and are committed to creating an inclusive environment for all employees. We are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Job DescriptionDescription: Job Brief We are seeking an experienced Sr. Design Engineer to provide leadership support to our Spinal Hardware Products team within the R&D department. The Senior Design Engineer will be responsible for the design, development, verification and validation of new and existing products for our spinal hardware portfolio. This role requires a strong technical background in mechanical engineering, desire to grow in leadership and the ability to collaborate effectively across teams. The Sr. Design Engineer will play a pivotal role in driving innovation, ensuring product quality, and meeting regulatory requirements in the spinal medical device sector. Responsibilities • Primary leader of assigned product development and sustaining projects., • Collaborate with cross-functional teams including R&D, Quality Assurance, Manufacturing, and Regulatory Affairs to achieve project goals and timelines., • Execute on the design, development, verification, and validation of new products, ensuring alignment with market needs and regulatory requirements., • Execute detailed mechanical component and assembly CAD models., • Generate detailed product drawings and component specifications., • Manage design transfer activities from R&D to manufacturing, optimizing processes and ensuring scalability., • Manage and prioritize sustaining engineering efforts for existing products, addressing design improvements, and manufacturing optimizations., • Implement corrective actions and continuous improvement initiatives based on post-market feedback and quality data., • Ensure compliance with FDA regulations (e.g., 21 CFR Part 820) for medical devices., • Collaborate with Regulatory Affairs to support regulatory submissions., • Minimum B.S. degree in Mechanical Engineering, Biomedical Engineering, or related field., • Minimum 5 years of experience in engineering roles within the medical device industry., • Strong background in medical device product development, including design, testing, and manufacturing processes., • Knowledge of materials selection, manufacturing processes (e.g., machining, casting), and product lifecycle management., • Experience in analytical processes (e.g., FEA, numerical modeling, Risk Analysis)., • Experience with contract manufacturer development and working relationships., • Experience with implantable medical devices or surgical instrumentation., • Familiarity with design for manufacturability (DFM) and design for assembly (DFA) principles., • Excellent organizational and communication skills., • Ability to prioritize tasks and manage multiple projects effectively. This is largely a sedentary role; prolonged periods sitting at a desk and working on a computer. This would require the ability to lift files, open filing cabinets and bend or stand as necessary. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Job Description Mastech Digital provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking a Testing/QA - Test Automation Engineer Senior for our client in the Retail domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a Contract position, and the client is looking for someone to start immediately. Duration: 6 Months Contract Location: Irving, TX (Onsite) Salary: $55.00-$60.00/Hourly Role: Testing/QA - Test Automation Engineer Senior Primary Skills: Quality Assurance Role Description: The Testing/QA - Test Automation Engineer, Senior must have 8+ years of experience. For this role, you must be an experienced QA Automation Engineer who can help automate the regression test suite and assist in documenting manual test cases for new features in the systems. Key Duties and Responsibilities: • Able to identify business risks and contribute to user story definition., • Experience in defining and reviewing Test Cases & Plans., • Creativity and thinking out-of-the-box as this project heart of store technology., • Experience in Device capability testing (WiFi Strength, Bluetooth etc.)., • Ability to come up with tools to simplify the testing effort for future hardware., • Prior experience with Mobile app automation (Android Preferred), Device Performance testing and Profiling for the applications., • Experience in writing automation frameworks from scratch., • Experience and in-depth knowledge of one or more programming languages (ex: JavaScript, Java, C#, etc.)., • Experience with one or more test tools & frameworks (ex: Selenium Web driver, cypress, Karate, JMeter, etc.)., • Team player mentality, actively cooperating with both engineering and non-engineering colleagues., • QA Mindset: We build stuff together, then break it and love doing it., • Degree in Computer Science or similar area of study., • Experience working in SCRUM environments., • Practical experience with web testing or development., • Experience with TDD, BDD / Gherkin., • Minimum 8 years of experience in QA automation, • Minimum 1 year of experience in Mongo DB, Node JS and AWS (Lambda, Step functions and cloud watch), • Knowledge or experience with pipelines, Jenkins, and CI / CD processes. Education: Bachelor’s degree/4-year degree Experience: Minimum 8+ years of experience Relocation: This position will not cover relocation expenses Travel: No Local Preferred: Yes Note: Must be able to work on a W2 basis (No C2C) Recruiter Name: Anshuman Garg Recruiter Phone: 484-331-9558 Benefits: We have various coverages and additional benefits to choose from: • Medical, Dental (Including Ortho) & Vision Insurance (Option to Enroll)., • Paid Leaves (Wherever applicable)., • Life & Disability Coverage (Upon eligibility)., • 401K Option, Education Assistance Program and more. Mastech Digital is an Equal Opportunity Employer - All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. #LI-AG1 #Mastech1

Job Description Position Summary: The Verification and Validation Engineer will be responsible for all activities related to the design verification and design validation (“V&V”) of Spectral MD, Inc. medical device(s). This includes, but is not limited to, defining, planning, documenting, leading, and/or performing all V&V activities. Essential Duties and Responsibilities: • Define, plan and lead activities, including, test method development and validation, fixture design and testing optimization in support of Design Verification and Validation., • Evaluate and analyze the system (entire device and any peripherals) performance and reliability to ensure the design is adequately pressure-tested to satisfy user, regulatory and business requirements., • Understand the system and subsystem design performance to identify and address early in the development process any potential design integration and design transfer risks., • Create and document test methodologies and provide feedback and recommendations for product/design changes., • Follow the Design Control Process and ensure compliance with the company’s quality policies, procedures, and practices., • Develop, document, and verify/validate test tools and test methodology for the verification of hardware (electrical, mechanical, imaging)., • Write and execute integration, plans, protocols, and associated reports., • Write and execute characterization, plans, protocols, and associated reports., • Write and execute verification plans, protocols, and associated reports., • Write validation plans and protocols and execute validation testing to demonstrate coverage of user needs and intended uses., • Analyze information and test data to support technical solutions., • Identify, report, and track defects identified throughout all phases of the development lifecycle., • Assist in quality systems responsibilities requested by management to ensure a robust and compliant Quality Management System Required education and experience: • Experience developing Class II and/or Class III medical devices., • A bachelor’s degree, or an advanced degree, in engineering, biotech, life sciences, or equivalent experience., • A minimum of five years’ experience in the medical device industry., • Working knowledge of the following regulations/standards:, • 21 CFR 820 and ISO 13485, • Risk Management per ISO 14971, • Highly detail-oriented, excellent analytical and troubleshooting skills, highly motivated team player adept at cross-functional interaction., • Excellent verbal and written communication skills., • Excellent interpersonal and customer service skills., • Excellent organizational skills and attention to detail., • Excellent time management skills with a proven ability to meet deadlines., • Strong analytical and problem-solving skills., • Ability to prioritize tasks and to delegate them when appropriate. The physical demands described below are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Prolonged periods of sitting at a desk and working on a computer. 15 % of travel time expected for the position, overnight to clinics or vendors. Equal Employment Opportunity: Spectral MD, Inc. is an equal opportunity and affirmative action employer. All applicants will be considered for employment without regard to race, color, ancestry, national origin, sex, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws.

We have an opening for a talented Netflix QA Tester to follow safety procedures and company policies, assist with organizing, stocking, and general upkeep, and manage daily responsibilities with a focus on quality and efficiency.

Utilizing Allen Bradley PLC, AutoCAD, and Ladder Logic Controls to design and implement complex engineering solutions. Providing technical support and guidance to the project team, ensuring all engineering aspects of the project are effectively managed. A bachelor’s degree in Engineering or a rela

Ensure all safety and quality standards are met.

Work with your team to maintain efficiency and service quality.

Help us succeed as our next Netflix QA Tester to perform responsibilities as a QA Tester.Stay adaptable to changing priorities and business needs.Stay adaptable to changing priorities and business needs.Perks include competitive pay, flexible scheduling, training opportunities, a supportive workplac

Help us succeed as our next Netflix QA Tester to perform responsibilities as a QA Tester.Stay adaptable to changing priorities and business needs.Stay adaptable to changing priorities and business needs.Perks include competitive pay, flexible scheduling, training opportunities, a supportive workplac

Work with your team to maintain efficiency and service quality.

Help us succeed as our next Netflix QA Tester to perform responsibilities as a QA Tester.Stay adaptable to changing priorities and business needs.Stay adaptable to changing priorities and business needs.Perks include competitive pay, flexible scheduling, training opportunities, a supportive workplac

Help us succeed as our next Netflix QA Tester to perform responsibilities as a QA Tester.Stay adaptable to changing priorities and business needs.Stay adaptable to changing priorities and business needs.Perks include competitive pay, flexible scheduling, training opportunities, a supportive workplac