Senior QMS Specialist/Document ContollerYatton, United Kingdom | Permanent, full-time
| £26,000 per annum
Our client, a well-known consumer products brand, have been operating to bring innovative, successful products to market for over 100 years. They currently have an urgent requirement to fill an essential quality/document control post in their manufacturing facility. The post will involve supporting the QMS Manager in establishing and maintaining Standard Operating Procedures (SOPs) for document management systems and control systems.
Key responsibilities include:
Compiling Product Quality Reviews (PQR`s)
Perform tasks related with the business’ supplier approval processes
Perform internal audits as required by the quality schedule to assure that the company remains compliant with the GMP requirements
Assist in the maintenance, administration and execution of the Change Controls & CAPA`s
Carry out staff quality training as necessary
Assist with external audits and regulatory inspections as required
Support QMS Manager with the creation of quality KPIs
Ensure data integrity
Deputise for the QMS Manager in their absence
To be successful in your application, you will need to demonstrate;
A proactive approach
The ability to work to deadlines
Ability to prioritise tasks and be comfortable working on own initiative
Confidence in using MS Office package, as well as the ability to learn quickly to manage different quality management software
Good organisational skills
English - fluent in speaking / writing
Experience with Good Manufacturing Practices in the context of pharmaceuticals would be a distinct advantage as would experience with validation activities. Flexibility and the capability of working alone with minimal supervision would be a key quality of the ideal candidate.
If you would like to apply for this role, please send your cv to us today for consideration.
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