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 will line manager a Quality Control team across the Leeds and Manchester GMP facilities.
Main Responsibilities
* Supervision of QC Inspectors
* Management of PDRs, allocating tasks, management of holidays, sickness, and training
* Allocation of QC Team Resource in line with production requirements at Leeds and Manchester
* Inspection and approval of clinical trial medicinal products
* Review of associated documentation
* Ability to prioritise workload and deal with changes to priorities to support a fast-paced ever-changing manufacturing environment
* Liaise and communicate with multiple departments to facilitate the on-time 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:
* Health Insurance
* Free onsite parking
* 25 days annual leave (increasing in increments to 30 days after 6 years' service)
* Your birthday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Please email maccareers@macplc.com should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.
Job Type: Full-time
Schedule:
* 8 hour shift
Work authorisation:
* United Kingdom (required)
Work Location:
* In person
Reference ID:
* HR389
#J-18808-Ljbffr