Quality Coordinator
- Maidenhead, ENG (GBR)
- £9 - £11 Per Hour
- 6 Months
- Start date: ASAP
- Ref: GSK0JP00075820
- quality assurance
- pharmaceutical
- documentation
- Regulatory compliance
- manufacturing
- gmp
- medical device
- ehs
Description:
Key purpose of this role:
• Support site staff to record all relevant information where there has been a deviation or unplanned event.
• Support of process technicians and line leaders to ensure quality based decisions are consistent with company values and patient focus.
• Support of the Batch Release process through the Quality review and approvals of GMP batch documentation and minor deviation reports.
The role will be based on the shift system.
Candidates should ideally be able to demonstrate:
Experience in quality assurance and compliance, manufacturing and/or development, working with consumer and/or pharmaceutical products.
Proven record of supporting of quality operations.
Knowledge working within GMP and EHS environments.
General knowledge of regulatory compliance requirements, including medical devices would be an advantage.
Excellent written/oral communication skills, interpersonal relationship building and team working skills.
All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.
