Quality Assurance Officer

Location
Edinburgh
Salary
Dependent on experience.
Posted
09 Oct 2019
Closes
06 Nov 2019
Ref
J5632327
Contact
Jessica McLachlan
Contract Type
Permanent
Hours
Full Time
Are you a Quality Assurance professional looking for your next role in industry? We are currently looking for a Quality Assurance Officer to join a growing innovative life sciences company based in the Edinburgh area. As the Quality Assurance Officer you will be responsible for supporting the busy Quality department in operation of the Quality Management System through ensuring compliance with GMP, ISO9001 and Human Tissue Act legislations for the manufacture of stem cells and other cell therapies for life saving clinical trials.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:

1. Reviewing and approving Incident Reports, Change Controls, Risk Assessments and SOPs to ensure compliance with GMP and other relevant regulatory requirements.

2. Supporting management of the company's Q-Pulse documentation system. Performing data review audits, including of Batch Production Records, Validation Documents and Development Documentation, in addition to supporting Validation activities.

3. Performing internal audits to determine compliance with GMP and to identify areas for improvement. Additionally, review and approve suppliers/service providers to ensure efficiency and effectiveness. As the Quality Assurance Officer, you will also support the QA Manager with hosting customer audits.

4. Provide Quality advice and guidance to the team, with support from the QA Manager. Similarly, providing excellent customer service skills for both internal and external customers.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Quality Assurance Officer we are looking to identify the following on your profile and past history:

1. Minimum BSc degree in a relevant life science subject.

2. Proven industry experience in a GMP Quality department, and with Grade A/B GMP clean rooms.

3. A working knowledge and practical experience with cell therapies or cell biology and using the Q-Pulse Document Management or similar system.

Key Words: cell therapy | stem cell | clinical trial | quality | QA | GMP | good manufacturing practice | ISO9001 | human tissue | cell biology | clean room | Q-Pulse

Apply for Quality Assurance Officer

Already uploaded your CV? Sign in to apply instantly

Apply

Upload from your computer

Or import from cloud storage

Your CV must be a .doc, .pdf, .docx, .rtf, and no bigger than 1MB


4000 characters left

Marketing Communication

We'd love to send you information about Jobs and Services from Chemistry World Jobs by email.

All emails will contain a link in the footer to enable you to unsubscribe at any time.


When you apply for a job we will send your application to the named recruiter, who may contact you. By applying for a job listed on Chemistry World Jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please email us.

Similar jobs

Similar jobs