Job Description
CooperSurgical is a leading fertility and women's healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. We deliver innovative assisted reproductive technology and genomic solutions that enhance the work of ART professionals. We offer over 600 clinically relevant medical devices to women's healthcare providers, including testing and treatment options.
CooperSurgical is a wholly‑owned subsidiary of CooperCompanies (Nasdaq: COO) and is headquartered in Trumbull, CT. The company produces and markets a wide array of products and services for use by women's health care clinicians.
Responsibilities
At CooperSurgical (CSI) we are currently recruiting a Senior Design Quality Engineer to our team in Falmouth, UK. You will be part of a team of experienced R&D engineers leading, designing, and testing our medical device products developed on site and across the Global R&D team.
In this role you will be responsible for ensuring the safety, effectiveness, and compliance of our medical devices throughout the design and development lifecycle. The role reports directly to the Manager of Design Engineering. Applicants must be eligible to work in the UK and be on‑site at Falmouth, Cornwall, UK.
Your Key Responsibilities
* Drive and lead validation processes, testing and verification
* Identify and manage risk
* Supplier engagement, evaluation and interaction
* Create and support continuous improvement
* CAPA / Non‑conformance
* Design reviews and evaluations
* Communicate key technical content to stakeholders
Qualifications
* BSc / BEng in Electronics, Electrical Engineering, Robotics, Mechatronics or combination of related fields.
* ≥ 4 years of experience from a similar role, preferably medical device production.
* Expertise in analog and digital circuit design and layout using tools like Altium Schematic Capture.
* Demonstrated skills in decision making across a broad spectrum of Quality Engineering responsibilities.
* Proven experience leading cross‑functional teams in a medical device development environment.
* Strong interpersonal, organizational and project management skills.
* Experience with Design for Manufacturing and Assembly (DFMA).
* Fluent English (spoken and written) is mandatory.
Additional Information
Seniority level: Mid‑Senior level. Employment type: Full‑time. Job function: Quality Assurance. Industries: Medical Equipment Manufacturing.
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