Details:
- Salary: £38,000 - 40,000 - Annum
- Job Type: Permanent
- Job Status: Full-Time
- Salary Per: Annum
- Location: Stoke-on-Trent Staffordshire
- Date: 2 days ago
Description:
We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.
That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.
As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.
The Role: Full Time (Monday to Friday) On-site
* Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
* Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
* Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
* Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
* Raising and overseeing the implementation of Change Controls and CAPA's when required
* Participating in site inspections by Regulatory Authorities
* Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
* Writing, reviewing and contributing to Risk Assessments
Benefits:
* Discretionary Bonus
* Healthcare & More
About You:
* Experience within a pharmaceutical environment
* A strong Quality Assurance background (2 to 3 years experience)
* Experience within sterile manufacturing environments (desirable)
* Good working knowledge of GMP requirements and quality systems
* Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
* Strong communicator and team player
* Confident using Microsoft Office products
If this sounds like a role that you have been looking for, click APPLY NOW