Quality Associate/manager - North West England, United Kingdom - Hyper Recruitment Solutions Ltd
Description
I'm currently looking for a Quality Associate/Manager to join a leading CRO based in the North West region.As the Quality Associate/Manager you will be responsible for the following:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Associate/Manager will be varied however the key duties and responsibilities are as follows:
- Carry out Audits of scientific data and documentation, ensuring that the regulatory studies are planned, executed and reported fully and accurately to adhere to GLP regulations.
- Deliver GLP training and mentoring to other junior members of the team, working closely with the Head of QA.
- You will carry out inspections of study procedures & laboratory processes ensuring they verify with GLP Quality compliance.
- Be able to give guidance and advice on CSV activities, including validation documentation complies with GLP regulatory requirements
ROLE REQUIREMENTS:
- Relevant Science or pharmaceutical related degree
- Proven industry experience within a Quality position in a GLP environment
- A working knowledge and practical experience working within a CRO
Key Words:
GLP, Quality, QA, Quality Assurance, Audit, CRO
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