Software Architect Salary at Voluntis Sa BETA

Job Description: Please provide a brief explanation of why you're interested in medical device technologies. Along with your rsum, please include a portfolio that shows some of your projects, skills, and processes. Be visual! Hybrid - This position offers a hybrid work schedule requiring you to be in the office 3 days a week and an option to work from home two days out of the week (unless a specific business need arises requiring in-office attendance on other days). Note that work schedules and office reporting requirements may change from time to time based on business needs. Ability to travel up to 10% nationwide. Individuals must possess a clean valid state driver's license to obtain the position. This position requires driving, therefore a valid driver's license and acceptable driving record are necessary. Additionally, because this position requires driving for company business as an essential function of the job, it must remain in compliance with company safety guidelines and pol

About SiFive As the pioneers who introduced RISC-V to the world, SiFive is transforming the future of compute by bringing the limitless potential of RISC-V to the highest performance and most data-intensive applications in the world. SiFive's unrivaled compute platforms are continuing to enable leading technology companies around the world to innovate, optimize and deliver the most advanced solutions of tomorrow across every market segment of chip design, including artificial intelligence, machine learning, automotive, data center, mobile, and consumer. With SiFive, the future of RISC-V has no limits. At SiFive, we are always excited to connect with talented individuals, who are just as passionate about driving innovation and changing the world as we are. Our constant innovation and ongoing success is down to our amazing teams of incredibly talented people, who collaborate and support each other to come up with truly groundbreaking ideas and solutions. Solutions that will have a huge i

We are partnered with a complex medical device manufacturer seeking a Document Control Specialist to join their team as they release a new product line. You will be working with the document control manager as you work through Change Controls, Trainings, and assist with eQMS implementation. Key Responsibilities: Maintain and manage document control systems in compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable regulations. Ensure proper documentation creation, review, approval, and archival in an electronic document management system (EDMS). Support the administration of change control processes, ensuring proper tracking, review, and implementation of changes to controlled documents. Work cross-functionally with Quality, Regulatory, Engineering, and other departments to ensure timely and compliant documentation updates. Perform periodic audits of controlled documents to ensure compliance and accuracy. Assist in training employees on document control procedures and best

The position reports to the Development Manager within the R&D/Product Development organization. The ideal candidate is an experienced software engineer who has experience developing front-end and back-end solutions while delivering high quality software using CI/CD workflows in an Agile/Scrum environment. This candidate will also possess superior communications skills and feel comfortable working on small multidisciplinary teams of engineers and scientists. All candidates must demonstrate software design and development experience in a majority of the following: •Understanding and appreciation of modern software design patterns and the application to real-world problems. •Understanding and usage of Entity Framework or other ORMs to access relational databases. •Understanding of modern practices for Authentication and Authorization. •Understanding of asynchronous design approaches: thread, callbacks, async await pattern •Development of User Interface software using modern approaches. •

Software Architect – Full Stack Location: Boston, MA Duration: FullTime About BigRio: BigRio is a remote-based, technology consulting firm with headquarters in Boston, MA. We deliver software solutions ranging from custom development and software implementation to data analytics and machine learning/AI integrations. As a one-stop shop, we attract clients from a variety of industries due to our proven ability to deliver cutting-edge, cost-effective software solutions. Role Overview As a Software Architect – Full Stack you will play a pivotal role in designing, developing, and maintaining web, mobile, and TV applications that power our cutting-edge radar-based device. This role blends architectural expertise with hands-on coding, requiring you to define system architecture, enable seamless integrations, and develop software that connects hardware, machine learning, and user-facing applications. You are a versatile engineer who effortlessly switches between front-end excellence, back-end

Position Title: Document Control Specialist or Blueprint Validation Auditor Project: review construction requirements outlined in blueprints and other technical documentation and validate against site requirements. Will ensure accuracy, detail, completeness and zero discrepancies. Project Objectives: Review all Specifications and Documents to collect the most recent updates Assess the technical requirements to construction requirements Validate construction requirements against the blueprints to ensure data integrity and track nonconformities. Develop a gap tracker and follow through to closure Skills: Strong knowledge of construction terminology and blueprints Attention to detail and exceptional organizational skills. Excellent communication skills, both written and verbal. Technical Document Control experience Experience reading construction blueprints a must

Job Details Level Experienced Job Location Westborough 0NK54 - Westborough, MA Position Type Full Time Job Category Manufacturing Description Summary: Creation and maintenance of assembly and customer documentation within the facility, in addition to coordinating ERP updates, as required. Essential Duties and Responsibilities: Upload, verify, edit and release bills of material into the ERP through new product introduction process. Perform ERP updates as required to ensure that standard costs, lead-times, operation numbers, AVL, planner numbers, lot control switches, and all other relevant ERP data are current. Assign ECO numbers and implement ECO changes in ERP. Maintenance of ECO process and attach completed ECOs to the ERP system. Update and link electronic documentation, as required. Execute line-for-line reviews of documentation to identify bill of material changes between the ERP and the customer-provided documentation. Create, maintain and distribute product folders, as required.

Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio and a global distribution footprint. We are the market leader in the development, manufacturing, and distribution of medical and aesthetic laser and light-based technologies. The Company’s technology enables physicians to provide advanced solutions for a broad range of medical-aesthetic application including hair removal, wrinkle reduction, tattoo removal, improving the skin’s appearance through the treatment of benign vascular and pigmented lesions, and the treatment of acne, leg veins, scarring and other common indications. Candela develops products for the global aesthetic market. These products begin as concepts developed by Candela’s world-class team of scientists and engineers or as acquired or licensed technologies that Candela then completes the development and/or commercialization of. These programs are supported by Candela’s global clinical, regulatory, and quality teams an