Quality Systems Associate
- Alva, Clackmannanshire
- £24,474-28,711 per year
- Permanent
- Full-time
Salary: £24,474 – £28,711 per annum, DOE plus benefits
Contract: Permanent, Full time
Hours: Monday – Thursday 8.30am-5pm Friday 8.30am-2.30pmAccuBio Ltd. (manufacturers of In vitro Medical Devices) are currently recruiting for a Quality Systems Associate.Job Role:As our Quality Systems Associate your main role is to coordinate the organisation’s activities required to meet quality standards and compliance to industry requirements.Main Responsibilities:
- Maintain the company’s quality procedures, standards and specifications.
- Review completed documentation to ensure completeness, accuracy and data integrity.
- Review and maintain customer requirements in relation to the company’s quality procedures, standards and specifications.
- Liaise with strategic sourcing staff to implement quality requirements from external suppliers.
- Assist with quality procedures and requirements in conjunction with operating staff.
- Maintain the quality management system via controlling documentation and records.
- Monitor the organisation’s quality performance by gathering relevant data.
- Monitor and progress of corrective and preventive action activities, complaint handling and the handling of nonconforming product and provide support and assistance as required.
- Review existing policies, make suggestions for changes and improvements and their effective implementation.
- Monitor the effectiveness of changes made and provide support as required.
- Advise Managers and Staff of the most appropriate quality processes to utilise that align with the group’s quality goals and culture.
- Advise Managers and Staff to conduct all work activities to maintain compliance with cGMP and other relevant quality standards.
- Assist in training staff across the organisation on internal quality orientated processes and culture.
- Carry out all duties and responsibilities to the company standard within the timescales required.
- Maintain compliance with Health & Safety policies and procedures.
- Maintain compliance with QMS policies and procedures.
- Maintain compliance with GDPR and Cyber Security policies and procedures.
- Perform any other reasonable duties and responsibilities as required
- A relevant degree or equivalent professional qualification
- Minimum of one year’s experience in a similar Quality Assurance role
- Strong organisational and administrative skills
- Proficient in both written and verbal communication
- Effective time management and prioritisation skills
- High attention to detail with a systematic and methodical approach to work
- Ability to work well under pressure, meet deadlines and adapt to changing priorities
- Self-motivated and capable of working independently or within a team
- Experience within the medical device sector or a similarly regulated industry
- Continuous Innovation
- Customer Orientation
- Challenge the Impossible
- Grow Together