QA Biocompatability Moderator

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the QA Admin will be varied however the key duties and responsibilities are as follows:

1.

Selecting the appropriate approved subcontractor
2.

Managing sample managements between the client, WML and subcontracting testing laboratory
3.

Reviewing GLP study Plans and liaising with the client on approval.


4.

Reviewing GLP study reports and liaising with the client on approval.

ROLE REQUIREMENTS:

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

1.

Relevant degree in a Life Science

2.

Proven industry experience and knowledge in GLP, ISO 17025, 10993 & 18562

3.

The ability to challenge and drive quality and a compliant culture forward and deliver against milestones.

Key Words: GLP / QA ADMIN / Biocompatibility Moderator / TIDS