Junior QA Engineer

Welland Medical Ltd; Crawley; On-site; GBP 25,000 - 35,000; Full time

Job summary

A medical equipment manufacturer in Crawley is seeking an Entry-Level Quality Assurance Engineer to support quality management systems and ensure compliance with ISO standards. The role involves calibrating production equipment, managing quality metrics, and assisting with audits and CAPAs. Ideal candidates have a degree in Engineering or a related field and are passionate about contributing to quality improvements in the medical sector. This is a full-time, onsite position with opportunities for growth.

Qualifications

• Promote adherence to QMS and ISO standards.
• Calibrate production equipment and maintain quality metrics.
• Provide support in quality audits and CAPAs.
• Assist with inspection and analysis of raw materials.

Responsibilities

• Ensure QMS compliance and manage ISO standards.
• Calibrate production equipment and maintain databases.
• Support manufacturing teams in quality assurance tasks.
• Assist with corrective and preventive actions (CAPAs).
• Foster teamwork and focus on key manufacturing KPIs.

Education

Degree in Engineering or related field

Job description

Welland Medical brings to market the best and most innovative products that enhance the lives of people living with a stoma across the world. Investing in the most talented people, collaborating to create world‑class, ground‑breaking products and services devoted to improving peoples’ lives. We are passionate about making a difference in the world. Our reputation is based on a tradition of improvement, ethical leadership, and total commitment to quality and safety.

Main Duties And Responsibilities

• Ensure the QMS is adhered to and that ISO standard requirements are met and maintained.
• Calibrate Production Equipment as necessary in a timely manner and maintain the calibration database; maintain and report on quality metrics.
• Support Manufacturing to ensure quality and material issues are dealt with and closed out in a timely manner.
• Assist with new material, Equipment, CSV, and Process validation as necessary.
• Assist in the improvements of QMS against ISO 13485.
• Support training to site staff on Quality System procedures as required.
• Assist with Corrective and Preventive Actions (CAPAs) and support CAPA teams as necessary.
• Assisting the business in closing CAPA and Non‑Conformances.
• Providing QA support and approval of CAPA and Non‑Conformances.
• Assist in Quality Audits (Internal, Supplier) against ISO 13485.
• Support for logging, monitoring, and closing audit actions, Internal, and Supplier.
• Work with manufacturing teams (Operations, Engineering and Planning Departments) in driving through the focus, teamwork and support required to ensure the delivery of all key manufacturing KPI’s.

Other Duties

• Support with customer complaints and complaint reporting.
• Assist Incoming Inspection sampling and analysis of raw materials.
• Support in post market surveillance (PMS) and post market clinical follow up (PMCF) activities.
• Contribute to Lean Manufacturing Projects and communicate progress to CI Management with regards to key KPIs.

A degree of flexibility is needed, and the job holder may be required to perform work not specifically referred to above and which will be appropriate to the level of the role.

For more information about the role or to apply don’t hesitate to get in touch with us [e-mail].

Seniority level

Entry level

Employment type

Full-time

Job function

Engineering and Information Technology

Industries

Medical Equipment Manufacturing

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