Job Description

Role Summary

The QMS Coordinator will support the day-to-day effectiveness of the business Quality Management Systems, ensuring compliance with all applicable regulations and quality standards for sourcing, procurement and logistics activities.

Role Responsibilities

o Maintenance, monitoring & improvement of the quality management system, including document control, deviations, complaints and CAPAs

o New supplier verification

o ISO internal audit schedule

Role Requirements

o Experience in quality management systems (minimum ISO 9001) is essential

o Experience in pharmaceutical and/or medical device regulations is preferred

o Proficient in Microsoft Office business suite

o Hours: Monday to Friday 9.30am to 3.00pm tbd (initially office based with possibility of flexible working after probationary period)

Personal Profile

o Advocator for quality first in all areas of business activities

o Able to work collaboratively and adapt to project needs and priorities

o Proactive and positive communicator with colleagues and other stakeholders

o Ability to drive own performance, demonstrate initiative, ownership and willingness to learn

o Excellent organisational skills and attention to detail

If you are passionate about maintaining high standards of quality and efficiency, we encourage you to apply for this exciting opportunity as a QMS Coordinator.

Job Types: Part-time, Permanent

Pay: 17,000.00-20,000.00 per year

Expected hours: 25 per week

Benefits:

Additional leave Bereavement leave Company pension On-site parking Private medical insurance Sick pay
Schedule:

Monday to Friday
Work authorisation:

United Kingdom (preferred)
Work Location: In person

Reference ID: QMS Coordinator