Quality Administrator - Abingdon, United Kingdom - Digby Morgan
Description
summary- _ abingdon, south east_
- _ £24,000 - £25,000 per year_
- _ contract_- specialism
- secretarial & admin- reference number
- QA
Position Title:
Quality Administrator
Position Job Profile and Job Family in Workday Contingent Worker Quality Assurance
ARDX Business Unit/Function:
Toxicology
Department:
QARA
Direct Manager:
Quality Systems Manager
Primary Location (Supporting Locations): Abingdon, UK...
Effective Date: 09-May-2023
Pay Rate:
£25,000 PA
The Client is a leading entity in diagnostic testing, committed to providing vital information for the treatment and management of diseases.
Our Toxicology Business Unit, situated in Abingdon, UK, is currently seeking a dedicated individual to fill the role of Quality Administrator.
In this position, you will play a crucial role in administering the maintenance of key Quality Management System processes, ensuring compliance and effectiveness across various departments.
Responsibilities:
- Review procedures for compliance with document control requirements.
- Ensure timely periodic review of documents.
- Manage the provision of controlled documents internally and externally.
- Review change orders/controls for compliance and track completion.
- Manage training assignments for new starters and ensure departmental training compliance.
- Generate metric and KPI information according to local and Divisional requirements.
- Support routine activities of the
QARA team. - Exhibit professional behavior consistent with company policies and practices.
- Perform other duties and projects as assigned.
Basic Qualifications | Education:
- Minimum three years' experience in organizations with a Quality Management System.
- Demonstrated excellence in administration skills.
- Previous experience in document and record control responsibilities.
Preferred Qualifications:
- Three years' experience in a medical device or laboratory testing organization.
- Awareness of ISO 13485, ISO9001, or ISO17025 requirements.
- Experience in reporting periodic KPIs/metrics to management.
Competencies:
- Strong organizational skills with a focus on detailed work.
- Excellent attention to detail in documentation review.
- Effective communication skills, both verbal and written.
- Ability to support colleagues onsite and remotely within the Quality Management System.
- Capable of driving completion of tasks through followup.
- Ability to manage multiple tasks in a fastpaced environment.
- Strong team player capable of taking instruction from multiple sources.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
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Position Title:
Quality Administrator
Position Job Profile and Job Family in Workday Contingent Worker Quality Assurance
ARDX Business Unit/Function:
Toxicology
Department:
QARA
Direct Manager:
Quality Systems Manager
Primary Location (Supporting Locations): Abingdon, UK
Effective Date: 09-May-2023
Pay Rate:
£25,000 PA
The Client is a leading entity in diagnostic testing, committed to providing vital information for the treatment and management of diseases.
Our Toxicology Business Unit, situated in Abingdon, UK, is currently seeking a dedicated individual to fill the role of Quality Administrator.
In this position, you will play a crucial role in administering the maintenance of key Quality Management System processes, ensuring compliance and effectiveness across various departments.
- Responsibilities:
- Review procedures for compliance with document control requirements.
- Ensure timely periodic review of documents.
- Manage the provision of controlled documents internally and externally.
- Review change orders/controls for compliance and track completion.
- Manage training assignments for new starters and ensure departmental training compliance.
- Generate metric and KPI information according to local and Divisional requirements.
- Support routine activities of the
QARA team. - Exhibit professional behavior consistent with company policies and practices.
- Perform other duties and projects as assigned.
Basic Qualifications | Education:
- Minimum three years' experience in organizations with a Quality Management System.
- Demonstrated excellence in administration skills.
- Previous experience in document and record control responsibilities.
Preferred Qualifications:
- Three years' experience in a medical device or laboratory testing organization.
- Awareness of ISO 13485, ISO9001, or ISO17025 requirements.
- Experience in reporting periodic KPIs/metrics to management.
Competencies:
- Strong organizational skills with a focus on detailed work.
- Excellent attention to detail in documentation review.
- Effective communication skills, both verbal
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