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Why work at Aqualution?
We encourage employees to share ideas and be part of decision-making
Weekly team huddles keep everyone engaged, informed, and connected
Ongoing training and Modern Apprenticeships help every individual grow
No zero-hour contracts – we offer Living Wage and flexible working for fulfilling careers
A zero-tolerance approach to discrimination, with robust policies ensuring dignity and fairness
A Team That Puts People First
At Aqualution, we believe in more than just work — we believe in purpose. Our employees are at the heart of everything we do, from pioneering stable hypochlorous acid solutions to advancing a more sustainable future. We foster a culture of engagement, development, and respect, making Aqualution a place where innovation thrives and careers flourish.
We proudly support the Fair Work First initiative, ensuring a workplace that prioritises employee voice, equal opportunity, and long-term career growth.
Current Openings
Reports to
Position
Location
Duns
Terms of employment
TOE
Job Summary
As a quality manager, you’ll coordinate the activities required to meet the quality standards set for certain products or services. You’ll ensure that this quality is consistent and meets both external and internal requirements.
Your role is concerned with monitoring and advising on the performance of the quality management system, producing data and reporting on performance, measuring against set standards.
To ensure the Quality and Environmental Management System (QEMS) is managed, monitored, developed and maintained, ensuring compliance with all applicable regulatory requirements.
As regulatory affairs manager the role is focused on completing gap analysis, completing remedial tasks, knowing MDR and UKCA regs for full technical file build (Clinical, risk, biological evaluations), and to be able to maintain the ISO13485 QMS system.
Main Activities
As a quality and environmental manager, you’ll need to:
- Maintain and update the company’s quality procedures, standards and specifications.
- Review customer requirements and make sure they are met.
- Work with purchasing staff to establish quality requirements from external suppliers.
- Set standards for quality.
- Make sure that manufacturing or production processes meet international and national standards.
- Identify ways to reduce waste and increase efficiency.
- Define quality procedures in conjunction with operating staff.
- Set up and maintain controls and documentation procedures.
- Monitor performance by gathering relevant data and produce statistical reports.
- Review existing policies and make suggestions for changes and improvements and how to implement them.
- Measure performance and identify any areas of weakness, recommending and implementing improvements.
- Liaise with other managers and staff and provide training, tools and techniques to enable others to achieve quality standards.
- Assess the effectiveness of changes made.
- Make sure the company is working as effectively as possible to keep up with competitors.
- Completion of risk management to ISO 13485 standards.
- Maintain procedures required by medical device.
- Monitor daily quality performance.
- Provide regulatory advice to obtain or maintain CE marking to EU medical device Regulation (EU/2017/745)
- Provide UKCA guidance to regulation (MDR2002)for medical devices classes I, IIa, IIb and III.
- Reviewing, collating, revising and updating technical files to meet UK and EU regulatory requirements.
- Risk management to ISO14971:2019
- Post market surveillance reports and plans.
- Post market clinical follow up.
- Communicate with notified bodies and competent authorities.
KPI’s and Monitoring
All KPI’s will be reported to the Operations Director once per month, prior to our Monthly Meeting.
- Customer Complaints
- Returns from Customers
- Audit performance / Adherence to schedule
- Time to completion of internal CAPA
- Time to complete external audit corrective actions
The role involves a high degree of physical work and therefore a good level of fitness is required.