Title: Supplier Quality Engineer Job Description: Role: SUPPLIER QUALITY ENGINEER Contract duration: 6 months Location: Lincoln - hybrid Hours per Day- 8 hrs and Hours per Week- 40 Contract: Inside IR35 - Paye rate: £30 p/h OR Umbrella rate: £40 per hour Our Client is an Energy technology company are seeking to recruit SUPPLIER QUALITY ENGINEER at Lincoln location. The role is for a contract position of 6 months Inside IR35. Our client has 150-year legacy of innovation and will focus on energy transformation, new technologies, decarbonization and Innovative leading-edge technology. A Snapshot of Your Day As a Supplier Quality Engineer (SQE) for blades and vanes (BV) supporting our Small Gas Turbine (SGT) business, you will be part of a growing team in a position that entails a large responsibility! Your day will be filled with interesting supplier interactions such as; addressing, processing and containing non-conformances, utilising your quality experience with tools such as 8D, RCA's and 5 why's, analysing data for trends and driving continuous improvement. You'll collaborate internally with experienced cross-functional teams to uphold client Energy quality standards, while fostering strong relationships with our valued suppliers. How You'll Make an Impact As a Supplier Quality Engineer you will be involved in Supplier Involvement and Collaboration: Engage with suppliers to help resolve process related issues, including non-conformance management and containment. You will Oversee supplier quality performance, including corrective and preventive actions, initiate quality improvement programs/initiatives and risk mitigation measures. You will be continuously monitor and report supplier quality performance, help contribute to KPI's and communicate risks and Support Product and Process Qualifications (PPQ), supporting suppliers in adhering to Energy Quality Management Processes and tools. What You Bring - Supplier Quality Engineer will have solid background in Engineering, R&D, or manufacturing is required (time served or degree qualified) and dealing with unexpected supplier quality issues from beginning to end. - Knowledge of inspection methodologies and capability. - Aerospace or similar industry experience. - Knowledge of drawing interpretation (Geometric Dimensioning and Tolerancing). - Knowledge in gas turbine blade/vane machining, casting and/or surface coating technology would be highly desirable. IT skills including excel/data manipulation. - Proficiency in quality methods (5 why, FMEA, 8D, RCA) and risk management, with a focus on product functionality, delivery/cost, and resource constraints. - Familiarity with Quality Management Systems (e.g. ISO9001), Supplier Quality Management (SQM) and Quality Control routines. - Understanding and application of ISO9001:2015 Interested in a fantastic career opportunity with a great pay rate?

Role Description You’ll work on a proven, high-performing mobile game built with Objective-C and Cocos, helping evolve it for the next stage of growth. This is not a “build from scratch” role—it’s about: - Improving a live product with real users - Making smart, high-leverage technical decisions - Using AI tools to accelerate development, debugging, and refactoring Qualifications - Strong experience with Objective-C and iOS development - Hands-on experience with Cocos (Cocos2d-x or similar) - Experience working on live mobile games or shipped apps - Ability to navigate and improve legacy codebases - Strong understanding of performance optimization (CPU, memory, rendering) - Pragmatic mindset: you know when to refactor vs. ship - Comfortable leveraging AI tools (e.g., Copilot, ChatGPT, etc.) as part of your workflow Requirements - Maintain and extend a legacy Objective-C + Cocos codebase - Optimize performance, memory usage, and runtime behavior for mobile - Refactor and modernize systems without breaking live operations - Ship features, events, and improvements in a live-service environment - Use AI-assisted workflows (code generation, debugging, refactoring, test creation) to move faster - Collaborate closely with product, design, and analytics to drive impact - Identify quick wins vs. deep tech improvements and prioritize accordingly Benefits - Market competitive, tax-free USD salaries - Paid Time Off - Performance Bonus - Annual Performance Reviews

Role Description The Professional Services Engineer is a hands-on technical contributor within Wunderkind’s Professional Services organization, responsible for implementing, integrating, and supporting customized client solutions. This role works closely with cross-functional Services teams and client stakeholders to translate business requirements into reliable, scalable technical implementations. The ideal candidate is a strong JavaScript engineer with experience building third-party integrations, validating data pipelines, and delivering production-ready solutions in a client-facing environment. Key Responsibilities - Develop, test, and maintain high-quality JavaScript and jQuery code to support end-to-end campaign requirements. - Implement client-specific technical solutions, including third-party integrations with client technology stacks (e.g., ESPs/CRMs, analytics tools). - Configure, validate, and support campaign setups within both Wunderkind’s internal platform and common ESP & CRM systems, ensuring alignment with technical and business requirements. - Partner with clients to test, validate, and support the implementation of client-facing SDKs (web and mobile app), including reviewing integrations, troubleshooting issues, and providing technical guidance and feedback. - Perform extensive data validation to ensure accurate data collection. - Execute functional testing and post-deployment validation to ensure campaigns and integrations perform as expected. - Collaborate with internal Delivery teams to ensure solutions align with platform standards and best practices. Qualifications - Strong proficiency in HTML, CSS, JavaScript, and jQuery with the ability to read and modify existing codebases. - Experience implementing and working with SDKs. - Proven experience building and supporting API integrations. - Hands-on experience using Git-based version control (GitHub and/or GitLab) in a collaborative workflow (branches, pull requests, code reviews). - Strong debugging, testing, and data validation skills. - Experience deploying and supporting production code in live client environments. - Familiarity with Email Service Providers (ESPs) such as Salesforce Marketing Cloud, Klaviyo, Braze, Bloomreach. - Experience with Go and/or PHP, preferred. - Experience with Airflow, preferred.

Title: (CW) Product Engineer / Medical Device and Combination Products Engineer(CONTRACT/TEMPORARY) Location: San Rafael United States Job Description: BioMarin is a leading, global rare disease biotechnology company focused on delivering medicines for people living with genetically defined conditions. Founded in 1997, the San Rafael, California-based company has a proven track record of innovation, with multiple commercial therapies and a strong clinical and preclinical pipeline. Using a distinctive approach to drug discovery and development, BioMarin seeks to unleash the full potential of genetic science by pursuing category-defining medicines that have a profound impact on patients.. About Technical Operations Our manufacturing and process development teams manage the production of our therapies for clinical trials and commercial markets. These engineers, technicians, scientists and support professionals continually provide quality assurance and ensure we meet all regulatory standards. We have manufacturing facilities in Northern California and in Shanbally, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution. CONTRACT ROLE APPROX 6 months ***Hybrid Position – Tues. Wed and Thurs. onsite in Novato*** About Technical Operations: BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. SUMMARY DESCRIPTION The Medical Device and Combination Products Engineer (Sr Engineer 2 Level 8) is responsible for development of medical device components of drug-device combination products. Primary activity is to manage and support design control, risk management and human factor engineering. The Engineer will lead internal device teams and will represent BioMarin to interact with technology and service providers, and contract manufacturers (CMOs) to ensure that all required activities are defined clearly and performed in a timely manner. RESPONSIBILITIES • Drive device and combination product development related engineering activities on critical pipeline products. This includes component and sub-assembly design, creating design history files, and leading technical project team meetings. • Create and own technical documentation (e.g. testing protocols, reports, SOPs, work instructions, etc.) • Manage / support device development including regulatory activities. • Support all regulatory filings and related activities. • Manage / Support all stages of design control for class II/III medical devices. • Interface with key stakeholders and outside experts / vendors to define project / product requirements to meet BioMarin’s Pipeline portfolio. • Specify test requirements and acceptance criteria to satisfy quality and regulatory needs (e.g. Design Verification Testing, DVT). • Lead / support risk analyses, such as hazard identification, FTA, FMEA etc., associated with devices. • Provide support to device component manufacturing and final product assembly with CMO. • Support human factor engineering studies with clinical sciences group. • As needed, facilitate product and process improvement through appropriate change controls and documentation. • Knowledge of regulations and standards (e.g.cGMP/QSR/ICH/ISO/AAMI/ANSI/FDA/EMA) • Working knowledge of design software packages e.g. SolidWorks an advantage. SCOPE This person will mainly be focused on ensuring Device Development activities to be performed per Regulatory guidance, industry practices and BioMarin’s SOPs. He/she will lead, support, and coordinate between various internal functions as well as external parties to ensure that devices / combination products meet predefined requirements. EDUCATION University degree in Engineering or related scientific discipline preferred, with 8-10 years related experience in medical device / combination product development. • University degree in Engineering or related scientific discipline preferred. Prefer MS with 8+ years or BS with 10+ years’ experience. EXPERIENCE • Experience managing cross functional programs is highly desirable. • Experience leading and coordinating human factor engineering studies • Experience to work in an out-sourced environment and to work with contract research, development, and manufacturing organizations is highly desirable. • Excellent written and verbal communication skills. • Must be comfortable with leading without authority, uncertainty and change. Desired Skills: • Device development, combination product development, auto injector, prefilled syringe, needle safety device, on body injector, on body device, vial and syringe development • Design history file, risk management (dfmea, ufmea, pfmea), design traceability matrix, design verification, design validation, process development • Design verification testing, report writing. Developing test methods • Design for assembly, design for manufacturability • Design input requirements, user requirements • Design output specification • Experience in working with external device component companies, vendors and CDMOs Manager is not interested in the following: • Lab technicians • Information technology engineers • Quality or regulatory engineers Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Equal Opportunity Employer/Veterans/Disabled 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, or protected veteran status and will not be discriminated against on the basis of disability.