We are currently looking for a Quality Systems Officer to join a leading Pharmaceutical company based in the Oxford area. As the Quality Systems Officer, you will be responsible for ensuring the highest standards of quality and compliance within the organisation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Systems Officer will be varied; however, the key duties and responsibilities are as follows:
1. Provide cross-functional support of GXP activities as they relate to Quality Systems, ensuring adherence to current Good Manufacturing Practice (cGMP) and inspection readiness.
2. Lead and participate in continuous improvement initiatives, reviewing records and documents for completeness and compliance with global regulations.
3. Support and manage the document lifecycle within the Electronic Document Management System (EDMS), tracking and trending compliance paperwork such as deviations and change controls.
4. Oversee training documentation and compliance metrics through the use of the Learning Management System (LMS), assisting with employee onboarding and ensuring organisational charts are regularly updated.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Systems Officer, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or technical field.
2. Proven industry experience in a regulated manufacturing environment.
3. A working knowledge and practical experience with validation of computerized systems, Microsoft Office applications, and EDMS.
Key Words: Quality Systems Officer / GXP / cGMP / Pharmaceutical / EDMS / Compliance / Continuous Improvement / Document Management / LMS / Internal Audit / Quality Metrics
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Systems Officer will be varied; however, the key duties and responsibilities are as follows:
1. Provide cross-functional support of GXP activities as they relate to Quality Systems, ensuring adherence to current Good Manufacturing Practice (cGMP) and inspection readiness.
2. Lead and participate in continuous improvement initiatives, reviewing records and documents for completeness and compliance with global regulations.
3. Support and manage the document lifecycle within the Electronic Document Management System (EDMS), tracking and trending compliance paperwork such as deviations and change controls.
4. Oversee training documentation and compliance metrics through the use of the Learning Management System (LMS), assisting with employee onboarding and ensuring organisational charts are regularly updated.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Systems Officer, we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or technical field.
2. Proven industry experience in a regulated manufacturing environment.
3. A working knowledge and practical experience with validation of computerized systems, Microsoft Office applications, and EDMS.
Key Words: Quality Systems Officer / GXP / cGMP / Pharmaceutical / EDMS / Compliance / Continuous Improvement / Document Management / LMS / Internal Audit / Quality Metrics
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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