Bracknell, 35 mi from Luton
Our Client is a Chemical Distributor. They are now seeking a Regulatory Compliance Administrator. This position will be office based near Bracknell, Berkshire and is a full-time permanent role.
This position is suitable for a Chemistry or Science...
MultiPassLondon, 30 mi from Luton
in the below text Make sure to read thoroughly, then apply.
MultiPass is a part of Dyninno group of companies which provides products and services in the travel, finance, entertainment, and technology sectors in 50+ countries.
As a Regulatory Compliance...
FinitasLondon, 30 mi from Luton
years 2nd line Risk and Compliance Experience within Payments
• Experience with Risk and Control Self Assessments
• Good understanding of FCA Regulations / Regulatory compliance
• If you are interested in the opportunity and have the relevant...
Martis SearchLondon, 30 mi from Luton
The company have an amazing working culture, invest a lot of money into technology and automation.
Our client is looking for someone who has a strong all round “Generalist Compliance” experience, but with particular leaning towards “Regulatory Compliance...
UrbnLondon, 30 mi from Luton
Title: Regulatory Compliance Manager Reports to: Senior Manager, Regulatory Compliance & Social Responsibility Overview URBN has a compelling opportunity within our Global Trade and Compliance department.
We're seeking a Manager of Regulatory...
Get new jobs by email!
Get email updates for the latest Regulatory Compliance jobs in Luton
It's free, and you can cancel email updates at any time
Operational Quality Manager - Aseptic Services
SRG | Luton | findajob.dwp.gov.uk |
Operational QA Manager requited for a sterile manufacturing company based in Luton
Skills and Experience
• Master's Degree in pharmacy.
• UK registered pharmacist.
• Minimum of 6 months experience in pharmaceutical industry.
• GMP knowledge and experience preferred.
• Strong literacy, written and numerical skills essential.
• Good IT skills.
• A keen team player who is supportive of work colleagues
• Enthusiastic in their approach to workload and capable of working towards KPI's
• An excellent communicator who is honest and respectful
In this role you will:
• Ensuring that all QPL licences and authorities are maintained and acting as the key contact for the MHRA and Home Office.
• Leading and closing any audits performed by the above authorities, or per customer/client.
• Monitoring and investigating trends in quality KPI's, namely fails, rework and complaints and report to the Board.
• Leading a culture of continuous quality improvement by constant monitoring and review of the Quality Management System.
• Promoting and educating colleagues in GMP (Good Manufacturing Practices) and GDP (Good Distribution Practices).
• Acting as Quality authorisation, signing off in conjunction with the Quality Director.
• Developing a strategy for the Quality Department with the Executive Directors to ensure continuous regulatory compliance whilst supporting business development and meeting board objectives.
• Providing Aseptic Quality input into the Management Review; ensuring outstanding issues are actioned and resolved, reporting to the Board if necessary.
• Providing quality information to other departments as required for new customer business, product, and service tenders.
• Leading, developing, and promoting the change management system within QPL including any validation requirements arising.
• Being able to act as a principal signatory for release of aseptically manufactured products.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Skills and Experience
• Master's Degree in pharmacy.
• UK registered pharmacist.
• Minimum of 6 months experience in pharmaceutical industry.
• GMP knowledge and experience preferred.
• Strong literacy, written and numerical skills essential.
• Good IT skills.
• A keen team player who is supportive of work colleagues
• Enthusiastic in their approach to workload and capable of working towards KPI's
• An excellent communicator who is honest and respectful
In this role you will:
• Ensuring that all QPL licences and authorities are maintained and acting as the key contact for the MHRA and Home Office.
• Leading and closing any audits performed by the above authorities, or per customer/client.
• Monitoring and investigating trends in quality KPI's, namely fails, rework and complaints and report to the Board.
• Leading a culture of continuous quality improvement by constant monitoring and review of the Quality Management System.
• Promoting and educating colleagues in GMP (Good Manufacturing Practices) and GDP (Good Distribution Practices).
• Acting as Quality authorisation, signing off in conjunction with the Quality Director.
• Developing a strategy for the Quality Department with the Executive Directors to ensure continuous regulatory compliance whilst supporting business development and meeting board objectives.
• Providing Aseptic Quality input into the Management Review; ensuring outstanding issues are actioned and resolved, reporting to the Board if necessary.
• Providing quality information to other departments as required for new customer business, product, and service tenders.
• Leading, developing, and promoting the change management system within QPL including any validation requirements arising.
• Being able to act as a principal signatory for release of aseptically manufactured products.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.
Best jobs you don't want to miss: