Gmp QA Associate - Leeds, United Kingdom - MAC Clinical Research

MAC Clinical Research

Verified Company

Leeds, United Kingdom

3 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.

We've an exciting opportunity for a hard-working individual who is capable of working independently and as team at our Leeds clinic in West Yorkshire.

Main Responsibilities

Inspection and approval of clinical trial medicinal products
Review of associated documentation
Assisting in root cause investigations for deviations and investigations for process improvements
Assisting in the completion and closure of corrective and preventative actions
Ensuring actions arising from Events, CAPAs, Risk Assessments, Self
Inspections and meeting minutes are followed up to completion
Liaise and communicate with multiple departments to facilitate the ontime release of products.

Key Skills and Requirements

Good interpersonal skills
Very good skills with Microsoft Office (e.g., Word, Excel)
The ability to write clear and concise reports
Good attention to detail and excellent organisational ability
Sufficient initiative to be able to work alone and with a team
GMP Production experience would be an advantage
Background in Microbiology, Chemistry or similar life science would be an advantage
Some experience in a clinical environment would be useful

BENEFITS:

Competitive salary in keeping with pharmaceutical industry standards and will reflect experience
Health Insurance
Free onsite parking
25 days annual leave (increasing in increments to 30 days after 6 years' service)
Your birthday off work

Benefits: