Jobs at Corin Group

Provides onsite IT support across Australian operations, serving as the first point of contact for helpdesk requests. Responsibilities include troubleshooting hardware, software, networking, infrastructure, and business applications; onboarding employees; maintaining systems; supporting Microsoft, Cisco, VMware, and Veeam environments; contributing to IT projects; documenting procedures; and ensuring compliance with ISO 13485 and ISO 27001 standards.

Administer payroll and employee records using Ceridian Dayforce, including starters, leavers, absences, pay changes, benefits, and compliance updates. Respond to payroll queries, support processing and audits, identify risks, liaise with pension and healthcare providers, and produce monthly payroll reporting. The role requires accuracy, confidentiality, strong organization, communication, payroll knowledge, HR systems experience, and Microsoft Office proficiency.

Designs orthopedic medical implants and instrumentation using CAD, FEA, and PLM tools. Develops design packages, manufacturing drawings, design controls, risk documentation, and technical reports. Collaborates with production, quality, regulatory, manufacturing, suppliers, customers, and bioengineering teams to support product introduction, compliance, CAPA activities, and existing product maintenance. Leads design problem-solving and contributes to project teams while following ISO 13485, GMP, FDA 21 CFR Part 820, SOPs, and safety requirements.

Own regional demand planning and forecasting, partnering with Sales and cross-functional teams to understand market demand, challenge assumptions, improve forecast accuracy, and support inventory, product launch, and investment decisions. The role requires maintaining planning data, presenting performance metrics, identifying risks and opportunities, and driving process improvements across international markets.

Supports supplier onboarding, qualification, development, second-source implementation, business integrations, product transfers, and NPI activities. Coordinates Supply Chain, Procurement, Quality, Engineering, Operations, Regulatory, and suppliers to track documentation, audits, tooling, samples, validation, corrective actions, and production readiness. Helps improve supply continuity and supplier resilience through risk assessment and improvement plans. Occasional work outside UK business hours and global travel may be required.

Develop, validate, and optimize manufacturing processes for regulated medical device technologies. Lead process transfers, new production launches, process verification and validation, automation, continuous improvement, PFMEA, root cause analysis, CAPA resolution, and manufacturing documentation. Maintain BOMs and technical records, collaborate with suppliers and NPI teams, and ensure compliance with ISO 13485, FDA 21 CFR Part 820, and GMP requirements.

Lead product and infrastructure cybersecurity, vulnerability management, customer and vendor security assurance, regulatory compliance, audits, incident response support, and security reporting for connected healthcare technologies. Partner with engineering, IT, hospital security teams, and external vendors while maintaining controls across the product lifecycle and Azure environments.

Investigates customer-reported product issues, performs root-cause analysis, analyzes technical data and system logs, and manages complaints through resolution. Supports sustaining engineering for released orthopaedic technology products, verification and validation testing, risk management, design controls, and technical documentation. Collaborates with production, quality, product management, sales, marketing, and customer service teams while contributing to continuous improvement and product safety.

Leads supplier quality management within a regulated manufacturing environment. Responsibilities include supplier development, audits, non-conformance investigations, root cause analysis, corrective and preventive actions, quality reporting, supplier performance management, and support for new product introductions. Ensures compliance with ISO 13485, GMP, FDA 21 CFR Part 820, and company quality systems while driving defect prevention, continuous improvement, and supplier readiness.

Maintain and update master data across business systems, process data requests, validate accuracy, investigate discrepancies, perform data audits and cleansing, produce reports, and support data quality improvements. The role collaborates with stakeholders across the business and requires strong Excel and Power BI skills, attention to detail, organization, and problem-solving abilities.

Leads cross-functional engineering execution for a software application supporting a robotic surgical platform. Responsibilities include sprint planning, milestone and budget management, dependency and risk tracking, software and hardware integration, systems engineering coordination, verification readiness, traceability, design reviews, and compliance with medical device regulations and standards.

Supports international distributor sales operations by coordinating marketing and training events, product registrations, documentation, forecasting, customer service meetings, returns, pricing, invoicing, and export project tracking. Acts as a key contact for distributor partners and collaborates with Finance, Marketing, Product Management, Regulatory Affairs, and Customer Services to resolve issues and support profitable global growth.

Lead the design and development of orthopaedic implants and instrumentation using CAD, FEA, and PLM practices. Review design outputs, mentor engineers, deliver design packages, support production transfer, and manage engineering changes and design-control documentation. Lead risk management, problem-solving, and CAPA-related design activities while collaborating with manufacturing, quality, regulatory, and project management teams. Support intellectual property generation, customer presentations, and compliance with medical-device regulations.

Manufacturing Production Engineer responsible for CNC programming, setup, operation, fault finding, process optimization, equipment performance, documentation, non-conformance management, tooling control, and continuous improvement. The role supports production flow, safety, OEE, cost reduction, and quality while training machinists and collaborating with engineering and maintenance teams. Weekend hours are Friday through Sunday, 05:30–18:30.

Owns the roadmap, backlog, requirements, prioritization, and cross-functional delivery of applications for a medical device surgical platform. Aligns customer, clinical, regulatory, commercial, and engineering needs; supports risk management, design reviews, technical investigations, and post-market feedback. Represents product progress to executives and ensures compliance with medical device standards, including ISO 13485, IEC 62304, and 21 CFR 820.

Develop and maintain full-stack software for a robotic orthopedic surgery platform. Build backend functionality in modern C++, Angular and TypeScript user interfaces, and interactive 3D visualization features. Collaborate with product, clinical, hardware, and external teams in an Agile environment. Ensure software quality through testing, reviews, verification, validation, and compliance with medical device standards including ISO 13485, IEC 62304, and Title 21 CFR 820.

Develops new medical device technologies, robotic systems, instrumentation, and hardware for hip and knee implants. Responsibilities include CAD modeling, structural calculations, tolerance analysis, design verification and validation, manufacturing documentation, testing, risk management, Design History File maintenance, and CAPA support. The role collaborates with quality, regulatory, clinical, manufacturing, and production teams while ensuring compliance with ISO 13485, GMP, and FDA requirements.

Manages Corin’s global customer experience and engagement programs, including visitor journeys, KPI dashboards, employee training, corporate presentations, customer events, congresses, and roadshows. Coordinates end-to-end visits for key stakeholders and industry leaders, gathers feedback, and drives improvements. Collaborates with Sales, Medical Education, Engineering, Marketing, Product Management, Legal, and Compliance while strengthening Corin’s brand and positioning in the MedTech industry.

Manufacturing Production Engineer serving as the CNC subject matter expert. Responsibilities include programming, setting, operating, troubleshooting, and optimizing CNC equipment; managing documentation and non-conformances; improving production efficiency, OEE, cost, and quality; managing tooling; training machinists; and supporting Kaizen, 5S, and workplace safety initiatives.

Develops and supports robotic medical technology devices and integrated hardware, software, firmware, and instrumentation systems. Responsibilities include systems architecture, requirements management, risk management, verification and validation planning, technical file and design history documentation, traceability, regulatory submissions, lifecycle support, and CAPA activities. Collaborates with R&D, quality, regulatory, manufacturing, marketing, subsystem owners, and project managers while adhering to ISO 13485 and FDA requirements.