QA Document Controller - Leeds, United Kingdom - MAC Clinical Research

MAC Clinical Research

Verified Company

Leeds, United Kingdom

1 week 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. The role will be based at Leeds although some cover maybe required at our Manchester site as required.

This is an onsite, part-time role (30 hours per week)

Main Responsibilities

Issuing, release and maintenance of the GMP Unit SOPs with applicable regulations.
Management of the GMP Unit SOPs, Forms and Template
Issuing release and maintenance of GMP Unit specific documentation
Assisting with the hosting of external audits or inspections from clients or regulators.
Assisting in facilitating quality improvements
Issue and Reconciliation of production forms for use
Maintenance of the GMP Training programs, including reminders and follow up
Maintenance of the GMP training log and trainer status

Key Skills and Requirements

Good interpersonal skills
Very good skills with Microsoft Office (eg Word, Excel)
Good attention to detail
Good communication and excellent organisational skills
Sufficient initiative to be able to work alone and with a team
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

Job Type:
Part-time

Expected hours: 30 per week

Benefits: