Quality Systems Administrator - part time

Expiring today

Location
Livingston
Salary
Dependent on experience.
Posted
26 Jul 2019
Closes
23 Aug 2019
Ref
J5631942
Contact
Jessica McLachlan
Contract Type
Permanent
Hours
Full Time
Are you a Quality Systems administrative professional looking for your next role in industry? We are currently looking for a Quality Systems Administrator to join an expanding, innovative medical devices company based in the Livingston area on a part time basis. As the Quality Systems Administrator you will be responsible for maintaining the effectiveness of the Quality Management System to meet ISO13485 standards and guidelines.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Quality Systems Administrator - part time will be varied however the key duties and responsibilities are as follows:

1. Maintain the document control register to ensure that all documents are correctly approved, current, and that their review date is maintained.

2. Maintain the CAPA system to ensure that all corrective and preventative action items are addressed by the appropriate action owner.

3. Ensure the training system is up to date and maintained, and co-ordinate any regulatory updates as advised by Quality Assurance and Regulatory Affairs consultants. Additionally, maintain customer feedback/complaints logs and work with appropriate personnel to co-ordinate responsive actions.

4. Assist with the internal audit programme and, as the Quality Systems Administrator, report to the senior management to assist with management reviews.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Quality Systems Administrator - part time we are looking to identify the following on your profile and past history:

1. Proven industry experience in a Quality Assurance environment with maintenance of a Quality Management System.

2. A working knowledge and practical experience with ISO 13485.

quality | QMS | quality management | medical devices | ISO | ISO13485 | quality standards | GMP | QA | quality assurance | QC | quality control | CAPA | SOPs | RA | regulatory affairs

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