Trabajos product developer en ShrewsburyCrear alertas

You'll own the technical direction of the platform, mentor senior engineers, and partner with product and engineering leadership to ship high-quality systems quickly. You'll balance roadmap delivery with engineering health: code quality, system reliability, on-call hygiene, and developer experience.

AMS is a world-leading independent developer and manufacturer of innovative tissue-healing technology, focused on quality outcomes for patients and value for payers. AMS has a wide range of surgical products including tissue adhesives, sutures, haemostats, internal fixation devices and internal sealants, which it markets under its brands LiquiBand®, RESORBA®, LiquiBandFix8®, LIQUIFIX™, Peters Surgical, Ifabond, Vitalitec and Seal-G®. AMS also supplies wound care dressings such as silver alginates, alginates, and foams through its ActivHeal® brand as well as under white label. Since 2019, the Group has made seven acquisitions: Sealantis, an Israeli developer of innovative internal sealants, Biomatlante, a French developer and manufacturer of surgical biomaterials, Raleigh, a leading UK coater and converter of woundcare and bio-diagnostics materials, AFS Medical, an Austrian specialist surgical business, Connexicon, an Irish tissue adhesives specialist, Syntacoll a German specialist in collagen-based absorbable surgical implants and Peters Surgical a global provider of specialty surgical sutures, mechanical haemostasis and internal cyanoacrylate devices. AMS's products, manufactured in the UK, Germany, France, the Netherlands, Thailand, India, the Czech Republic and Israel, are sold globally via a network of multinational or regional partners and distributors, as well as via AMS's own direct sales forces in the UK, Germany, Austria, France, Poland, Benelux, India, the Czech Republic and Russia. The Group has R&D innovation hubs in the UK, Ireland, Germany, France and Israel. Established in 1991, the Group has more than 1,500 employees. For more information, please see www.admedsol.com • Create and maintain Regulatory Technical Documentation in compliance with European, USA markets, and other global territories including 93/42/EEC, (EU) 2017/745 and 21 CFR Part 820 requirements., • Maintain continued product regulatory approval for the European, USA markets, and other global territories., • Contribute to regulatory strategy planning and change management., • Perform post market surveillance activities such as vigilance reporting, customer feedback, post market clinical trends and pro-active market feedback., • Maintain the Pre-Market and Product Life Cycle processes and SOPs., • Prepare regulatory documentation for submissions of changes to existing devices for European, USA markets, and other global territories., • Support the creation of European, USA, and other global territories, strategy documentation for changes to existing devices., • Review and approve documentation in support of Design History File compilation e.g. design inputs/outputs, clinical evaluation reports, risk management., • Compilation of the application FMEA in support of Risk Management., • Support the assessment and submission of quality management systems changes to regulatory authorities in European, USA, and other global territories, with input from other functions as required., • Create, schedule and ensure adherence of Regulatory Technical Documentation updates., • Provide regulatory input to major extensions to existing product lines and changes., • Implement and maintain the post market surveillance process and SOPs., • Review and analyse adverse event trending during PMS cycles., • Support complaint reduction, and product performance improvement programmes., • Support Risk Management System activities by supplying post market data to key internal stakeholders., • Support product performance and manufacture process improvement programmes, to ensure compliance with Regulations and directives from European, USA markets, and other global territories including 93/42/EEC, (EU) 2017/745 and 21 CFR Part 820 requirements., • Responsible for preparation and approval of Incident Reporting and FSCA/Recall reporting to meet regulatory requirements worldwide., • Establish, manage and maintain good relationships with Regulatory Authorities and be the point of contact in respect of Vigilance (Incident Reporting, FSCA/Recall)., • Liaise with customer and Registration Holder for Incident Reporting and FSCA/Recall activities, within the terms of existing contractual obligations., • Review and approval of key compliance records e.g. labelling, Instructions for Use (IFU)., • Generation of product labelling requirements., • Establish, manage and maintain good relationships with Regulatory Authorities and be the point of contact in respect of regulatory submissions., • Liaise with customers for Regulatory discussions, within the terms of existing contractual obligations., • Act as Regulatory Subject Matter Expert for the preparation and participation in audits including FDA inspections, Notified Body and Global Authority and customer audits., • Responsible for regulatory review of Regulations and Guidance, learn and understand changes, monitor and ensure conformance by implementing procedural updates., • Interpret and apply medical device regulations to ensure conformance within the business, relevant to this role., • Maintain catalogue of learnings from regulatory submissions and technical audits., • Collaborates and interacts with internal teams, including Regulatory Affairs, Clinical, Quality, Engineering, Operations, Sales, Marketing, Customer Services., • Promote and demonstrate the Company Values in the workplace., • Promote health and safety policies in the workplace., • Degree, or equivalent qualification, in a Life Science, or equivalent industry experience., • Knowledge of relevant GMP and Quality Systems standard, specifically with FDA Quality System Regulation and ISO 13485 relevant to this role., • Understanding of the European Medical Devices Regulation (MDR) relevant to this role., • Experience in preparation of and obtaining 510(k) clearance would be preferable., • Experience in preparation and obtaining Design Dossier approvals would be preferable., • Experience in maintaining technical files., • Experience of working in a regulated environment., • Understanding of Risk Management within a Medical Device industry., • Ability to query and analyse data., • Demonstrated organisational skills., • Ability to work under pressure to meet process/project time frames, regulatory requirements and company requirements., • Competent IT skill in preparing files., • The ability to influence and challenge others in a constructive way to deliver improvements., • Excellent communication skills both written and verbally with employees, customers, and Regulatory Authorities. #J-18808-Ljbffr

Salary: £55,000 - £65,000 per annum Employment type: Permanent Hours per week: 37 Reporting into: Lead Integration Developer Department: IT Click here to read the full job description and view our excellent benefits here This role operates primarily on a remote working arrangement that will require little to no travel into our Coventry head office or local campus. Our working model arrangements are a non-contractual benefit so please note that an Arden work location is added to our employment contracts. About Arden University : We are an aspirational and multi-award-winning university, delivering rapid growth with ambitious plans to disrupt the HE sector through our passion for innovation and digital education. Our vision is to become the first-choice university for career-focused lifelong learners worldwide, ensuring that everyone, everywhere can access higher education. There has never been a more exciting time to join Arden University, as we expand into new disciplines, forge worldwide partnerships, and expand our locations. About our Department : This Software Engineer role sits within the Cloud Platform team as part of the wider IT Department. The Team is responsible for the design, development and continuous enhancement of the organisation's middleware solutions and integration services. The wider IT team is made up of around 60 employees with a vast range of skills from Software Development to IT Operations and IT Security. Our IT Department values employee development and we have lots of great examples of employee progression and promotions within the team. About the Opportunity: The role plays a critical part in enabling reliable message delivery, translation and validation between core business platforms through the ownership of a robust, scalable and future proof middleware products. By embedding complex and non-standard requirements within a flexible middleware framework, the role empowers the business to unlock advanced capabilities and realise process improvements that would otherwise be difficult to achieve. Their work drives the organisation’s evolution toward a well-architected, seamlessly integrated ecosystem of products and services. The role also carries operational responsibility for the performance and reliability of the middleware platform in production, including the delivery of secure and compliant integrations that meet internal standards and industry best practices. Working closely with development teams, product managers, and other stakeholders, the Software Engineer (Cloud & Integration) ensures that integration solutions are aligned with both technical objectives and evolving business needs. About You: Essential requirements: Deep working knowledge of relevant AWS services; primarily Lambda, API Gateway, SNS/SQS, S3, Dynamo DB, IAM and Cloud Watch. Solid understanding of software development principles, including design patterns, architecture, and methodologies - particularly in middleware and service integration. Practical knowledge of event-driven architectures, leveraging services such as SNS, SQS, and Lambda triggers Hands-on experience working in a Dev Ops environment, utilizing infrastructure as code (Ia C), automation, and CI/CD pipelines. Desirable requirements: Why Arden: At Arden, you will become a part of a passionate and dedicated team who are committed to removing unnecessary barriers to learning and making education more accessible. Our people work hard to ensure our students journeys are the best they can possibly be, as such we want to reward our people with fantastic benefits. Employees benefit from: 30 days holiday + bank holidays on-top, and even a Christmas closure! A generous Aviva pension plan, company contributions starting from 7% Simply Health plan option Private Medical Insurance coverage (applies to certain job roles) Access to Perkbox benefits Study any Arden course for free, with a discount for all family and friends Plus, other excellent benefits Our ‘Golden Ticket’ which allows you to gift anyone in your life a free Arden education Our Values: Stand out, Progressive, Accessible, Resourceful, Kindness, reflect who we are as an institution, a team and as individuals. If they also reflect you and you are excited by the chance to be the driving, creative force within a growing business, we want to hear from you. There has never been a more exciting time to join Arden University, as we expand into new disciplines and locations. Closing Date: 20th Aug We reserve the right to close this vacancy before the specified closing date should we receive sufficient applications or in order to respond to business needs. In order to avoid missing an opportunity to apply please submit your application as early as possible. If you are a current Arden student or have an upcoming course with us, you are not eligible to apply for Student Experience roles due to a conflict of interest related to system access. Equity, Diversity & Inclusion: Arden University is proud to be a Disability Confident Employer. This means that if you have a disability, as defined by the Disability Equality Act 2010, you may be guaranteed an interview if you meet the essential criteria for the role. If you wish to be considered under this scheme, you can indicate via the application form below. By doing so, you are also consenting for this information to be shared with the hiring team. For more details on what qualifies as a disability under the Disability Equality Act 2010, please refer to the guidance here. As an Equal Opportunity Employer we celebrate diversity and are committed to creating a diverse and inclusive workplace. Therefore, we make sure that our recruitment and selection processes never discriminate based upon people's age, disability, gender, race or ethnicity, religion or belief, sexual orientation, or other personal circumstances, and actively welcome applications from all groups. Sponsorship statement: Please be aware that some roles may not meet the points requirement for a sponsored Skilled Worker visa under the points-based immigration system. However, we welcome applications from candidates who do not currently have the right to work in the UK but may be eligible for a visa through an alternative route.

The Customer Order Engineering Manager will lead the Shrewsbury Customer Order Engineering team, ensuring timely and accurate execution of customer orders while maintaining compliance with company standards. This role oversees customer specification reviews, Bills of Materials, and manages engineering data for manufacturing drawings. Key responsibilities include guiding conceptual design, material selection, and testing; configuring products using CAD tools; and providing technical support to internal teams, customers, and vendors. The manager will drive process improvements, develop new engineering tools, maintain documentation, and collaborate with global engineering hubs. Additional duties include mentoring engineers and design staff, coordinating schedules, and supporting product validation and certification compliance. Supervise the group in creating engineering data required for developing manufacturing drawings. Determine and verify component dimensions, tolerances, suitable materials and finishes, and prepare necessary supporting calculations. Responsibilities include conceptual engineering, material selection, design and analysis, prototyping, and testing. Ensure products meet established requirements and apply sound engineering practices, considering the cost-effectiveness and quality impact of technology used. Lead and participate as needed in configuring products using 2D and 3D CAD software and assist in generating detailed drawings and schematics. Assess suitability and generate engineering data for third-party products as needed to meet customer specifications. Support materials management in identifying vendors when required. Provide technical information and guidance to vendors and suppliers of valve components or external services. Initiate and contribute to the development of new engineering tools and the improvement of workflows and methodologies both locally and in collaboration with the global COE team, including software and system advancements. Collaborate with Product Managers on product validation to ensure compliance with external certification standards. Offer technical support to other departments and customers, including in-house and field analysis related to product performance issues raised by customers. Provide technical input to various departments, engineering groups, Project Management, Order Management, and Manufacturing. Respond to Valve Automation product inquiries; supply design information and discuss advantages. Participate in order teams and develop training materials for new technologies and products. Guide and review the work of less experienced engineers and drafting/design staff, and oversee designers and technicians involved in developing and testing new product concepts. Specify analytical and test equipment, facilities, and techniques as required. • Bachelor's degree in Mechanical Engineering or related technical discipline., • 7+ years of engineering experience within industrial manufacturing, automation, flow control, valves, actuators, or related industries., • 3+ years of experience leading engineering teams, including coaching, performance management, and talent development., • Strong understanding of mechanical design principles, engineering mechanics, materials, and manufacturing processes., • Proficiency with 3D CAD software (SolidWorks preferred) and AutoCAD., • Experience supporting customer-specific engineered-to-order (ETO) products is highly preferred., • Working knowledge of FEA, GD&T, statistical analysis, and product validation methodologies., • Strong project management, communication, and cross-functional leadership skills., • Experience working with global engineering teams and driving continuous improvement initiatives is preferred. We offer a dynamic work environment that values innovation and suits development-minded people who enjoy working in a fast-paced and energetic setting with opportunities for continual growth. We're looking for team-oriented people with a willingness to learn and contribute to our customers’ success. This includes a generous wage starting between $110k-130k/annual* and benefits package that offers a 401k with company match as well as company funded pension. *Salary range is intended to provide a general guideline. Actual compensation will be determined based on market data, internal equity, and candidate credentials.” Please note that any offer of employment is contingent upon a background check and pre-employment physical and drug screen. Delivering competitive technologies and services is what we do best. At Valmet, we continue to push forward and develop ourselves, concentrating on technology, services, sustainability, local presence, and our people. Valmet is where the best talent from a wide variety of backgrounds comes together. With 19,000 professionals around the world, we are the leading global developer and supplier of technologies, automation and services for the pulp, paper and energy industries. Our commitment to moving our customer's performance forward requires creativity, technological innovations, service know-how - and above all, teamwork. #J-18808-Ljbffr

As a Full-Stack Product Developer, you’ll collaborate with a highly skilled team of engineers to build features from concept to deployment. The Role Are you passionate about building impactful products in a greenfield environment? Our mission is to build a data stewardship platform that will strea

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Our client global workplace design and construction partner with 45+ years' experience, delivering projects across 100+ cities in 37+ countries.The Amsterdam office is a hub for pan-European delivery, combining continental reach with local knowledge, supply chains and standards.Their recent work inc

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