5 of 5 ISO 13485 Jobs in the Midlands

also lead improvements that reduce turnaround times, streamline processes, improve reporting, introduce best practice and prepare the department for future regulatory requirements, including ISO 13485 compliance. Why This Role Is Unique This isn't a typical service leadership role. You'll be working at the intersection of: Assistive … genuinely meaningful. What success looks like in 12 months: Reduce repair turnaround times. Improve first-time fix performance. Strengthen reporting and KPIs. Support ISO 13485 readiness. Build strong relationships across Engineering, Production and Customer Services. What We're Looking For We're looking for a rare combination ...

teams. Build and grow relationships with strategic medical and scientific clients. Create proposals, project plans, budgets and commercial quotations. Ensure projects are delivered within ISO 13485 quality requirements. Support business development activities, client presentations and industry events. About You We're looking for an accomplished engineer and project … leader with a proven track record in medical product development. You will have: Significant experience delivering medical device development projects within an ISO 13485 environment. Strong project management and commercial awareness, including budgeting, quoting and client management. Experience leading multidisciplinary engineering teams. A degree in Mechanical Engineering, Mechatronics ...

operational experience in Quality within a regulated industry such as manufacturing, medical devices, pharmaceuticals, aerospace, automotive, or food and beverage Applied, working knowledge of ISO 9001:2015 and at least one sector-specific standard (e.g. ISO 13485, AS9100, IATF 16949, or FDA 21 CFR Part 820), gained ...

environment, ideally medical devices. Experience working within structured development processes covering requirements, traceability, risk management, testing and V&V. IEC 62304 and/or ISO 13485 experience would be highly advantageous. This is a fantastic opportunity to join a growing MedTech business at an exciting stage of development ...

regulated environment. Familiarity with document management or OCR tools. Experience using Jira and Confluence. Awareness of clinical governance or quality frameworks (for example GxP, ISO 13485, DCB0129/0160). What success looks like in the first 6 months Full ownership of e-sign configuration and first-line ...