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R&D Quality Administrator
Hyper Recruitment Solutions LTD
L1, Liverpool, Merseyside, Merseyside
Full-Time
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We are currently looking for a R&D Quality Administrator to join a leading Biotechnology company based in the Liverpool area. As the R&D Quality Administrator you will be responsible for
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the R&D Quality Administrator will be varied however the key duties and responsibilities are as follows:
1. Generate and manage documents and SOPS within the QMS
2. Maintain and Implement QMS in conformance with quality policies
3. Evaluate trends and compliance levels and report any issues to senior management
4. Provide document creation support to ensure all documents are formatted to company standards and are cGMP compliant.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the R&D Quality Administrator we are looking to identify the following on your profile and past history:
1. Relevant degree in a Scientific discipline
2. Proven industry experience working with Quality management systems within a GMP environment is vital
3. A working knowledge and practical experience with various Pharmaceutical quality systems is a must
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the R&D Quality Administrator will be varied however the key duties and responsibilities are as follows:
1. Generate and manage documents and SOPS within the QMS
2. Maintain and Implement QMS in conformance with quality policies
3. Evaluate trends and compliance levels and report any issues to senior management
4. Provide document creation support to ensure all documents are formatted to company standards and are cGMP compliant.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the R&D Quality Administrator we are looking to identify the following on your profile and past history:
1. Relevant degree in a Scientific discipline
2. Proven industry experience working with Quality management systems within a GMP environment is vital
3. A working knowledge and practical experience with various Pharmaceutical quality systems is a must
Recommended skills
Pharmaceuticals
Management
Certified Global Meeting Planner
Good Manufacturing Practices
Quality Management Systems
Job ID: 212960822
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