Create a Job Alert.
Enter your email below to save this search and receive job recommendations for similar positions.
Thank you.
We'll send jobs matching these to
You already suscribed to this job alert.
UK
You’re being taken to an external site to apply.
Enter your email below to receive job recommendations for similar positions.
Quality Assurance Officer
P&S Personnel
Great Yarmouth, Norfolk, Norfolk
Full-Time
Create Job Alert.
Get similar jobs sent to your email
P+S Personnel are pleased to be working on behalf of our clients, who are currently seeking a Quality Assurance Officer to join their team based in Great Yarmouth on a full-time, permanent basis.
This role reports to the Quality Assurance Manager
Key responsibilities
* The control, preparation, review and approval of Quality documentation
* Assisting other QA colleagues with developing GMP and quality related training programmes, including delivering training.
* Responsibility for maintaining up-to-date training records for all staff
* Investigating and monitoring breaches of GMP which may arise in the manufacture, testing and supply of materials.
* Recommending corrective and preventative actions and monitoring implementation of these recommendations.
* Assisting with the scheduling and performance of internal audits with responsibility for the progression and monitoring of corrective actions.
* Performing the review of batch documentation prior to release by the QP.
* Supporting quality projects.
Qualifications
* BSc or equivalent in a relevant scientific discipline.
Skills and Experience
* Some experience in a pharmaceutical environment would be an advantage.
* Computer literate to include MS Word and Excel.
* Good inter-personal skills and the ability to communicate well in English both written and orally.
* Good attention to detail and documentation skills
If this is a position you are interested in, then please apply ensuring your CV is up to date
This role reports to the Quality Assurance Manager
Key responsibilities
* The control, preparation, review and approval of Quality documentation
* Assisting other QA colleagues with developing GMP and quality related training programmes, including delivering training.
* Responsibility for maintaining up-to-date training records for all staff
* Investigating and monitoring breaches of GMP which may arise in the manufacture, testing and supply of materials.
* Recommending corrective and preventative actions and monitoring implementation of these recommendations.
* Assisting with the scheduling and performance of internal audits with responsibility for the progression and monitoring of corrective actions.
* Performing the review of batch documentation prior to release by the QP.
* Supporting quality projects.
Qualifications
* BSc or equivalent in a relevant scientific discipline.
Skills and Experience
* Some experience in a pharmaceutical environment would be an advantage.
* Computer literate to include MS Word and Excel.
* Good inter-personal skills and the ability to communicate well in English both written and orally.
* Good attention to detail and documentation skills
If this is a position you are interested in, then please apply ensuring your CV is up to date
Recommended skills
Scheduling
Product Quality Assurance
Quality Assurance
Documentation
Auditing
Job ID: 212956542
JOBMEDIC.CO.UK TIP
For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.
By applying to a job using Jobmedic.co.uk you are agreeing to comply with and be subject to the Jobmedic.co.uk Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.