Quality System Administrator II in Falmouth

Company Overview

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. As a division of CooperCompanies, we are driven by a unified purpose to enable patients to experience life's beautiful moments. Our values—dedicated, innovative, friendly, partners, and do the right thing—guide our support for patients throughout their lifetimes, from contraception to fertility and birth solutions, to women’s and family care, and beyond. We offer over 600 clinically relevant medical devices, including testing and treatment options and an innovative suite of assisted reproductive technology and genomic testing solutions.

Scope

The Quality Coordinator supports the Quality Department at Research Instruments, Falmouth, UK. The role supports the Quality Manager in maintaining overall site compliance with ISO 13485, FDA 21 CFR Part 820, and MDSAP requirements by managing Quality Management System documentation and records, particularly employee training records, and providing data for quality metrics monitoring.

Job Summary

The Quality Coordinator supports quality systems, regulatory compliance, and continuous improvement within Research Instruments. Key responsibilities include:

• Managing quality documentation, coordinating employee training and maintaining accurate training records.
• Ensuring adherence to regulations and standards.
• Gathering quality data for KPI monitoring and monthly trending.
• Collaborating with various departments to resolve quality issues and improve processes.

Responsibilities

• Manage and maintain quality documents, records, and quality system procedures to ensure compliance and traceability.
• Gather data and report on KPIs to measure Quality Management System performance.
• Effectively monitor and communicate quality management system performance metrics, reporting monthly trending and supporting Management Review.
• Identify Quality Management System-related non-conformances and identify trends that require escalation.
• Maintain the Training Matrix and support the Quality Manager with the update of supplier status and Quality Agreements.
• Assist with Internal Audits and maintain evidence of follow-up actions.
• Support in preparation for and hosting of external audits.
• Assist with Corrective and Preventive Action (CAPA) root cause investigations and maintain evidence of follow-up actions.
• Support with any other Quality-related investigations and improvements as directed by the Quality Manager.
• Take part proactively in the QA team and ensure good cross communication between QA team members and those of other departments to meet business demands.
• Collaborate closely with cross-functional RI teams to resolve quality issues quickly and avoid disruptions.

Travel

Travel to sister sites and suppliers may be required, < 10% of the time if so.

Qualifications

• A strong focus on accuracy and thoroughness is crucial for quality work.
• Ability to identify issues, conduct root cause analysis, and implement solutions.
• Strong written and verbal communication skills to interact with various internal and external stakeholders.
• Ability to work collaboratively as part of a quality team and with other departments.
• Familiarity with conducting data analysis and reporting statistics.
• Knowledge of ISO 13485, FDA 21CFR part 820 and MDSAP is desirable.
• Excellent organizational, time management and communication skills are needed to handle multiple priorities effectively.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) is essential for reporting and documentation.
• Expertise in MS Office and Adobe Acrobat is desirable, including the creation of locked, fillable forms in both Word and Adobe.

Work Environment

Office environment in a shared workspace. Moving about the site and on the shop floor where care is needed. Nature of work may include long periods of intense concentration, frequent interruptions, multiple tasks and meeting deadlines.

Experience

• Previous relevant experience in a Quality Assurance or Quality Control role in a regulated industry, medical device preferred.
• Experience in ISO13485 quality systems is preferred.
• Experience in writing technical documents such as policies, procedures, assessments, and reports.
• Experience with document control and GMP.

Education

Degree level qualification or equivalent.

Seniority level: Entry level

Employment type: Full-time

Job function: Quality Assurance

Industries: Medical Equipment Manufacturing