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The Quality Administrator will support the Account Quality Lead in ensuring compliance with client procedures and cGxP regulations for JLL's IFM services. This role is crucial in maintaining the quality management system, handling documentation, and assisting with various administrative tasks to support the quality assurance process.
Key Responsibilities
Documentation Control:
Manage and organize quality-related documents in both physical and electronic formats
Maintain and update the SharePoint organization system for efficient document retrieval
Ensure proper archiving of quality records and documents
Quality System Support:
Assist in the implementation and maintenance of the JLL Life Sciences QMS at the account level
Support the development and revision of Standard Operating Procedures (SOPs), Work Instructions (WIs), and forms
Help maintain compliance with client SOPs, contractual agreements, and JLL best practices
Data Management and Reporting:
Create and maintain quality reports, designs, and charts for data analysis
Assist in the development and updating of KPI dashboards
Track and report on quality metrics and trends
Corrective and Preventive Actions (CAPA) Management:
Monitor and follow up on open CAPAs and work orders
Assist in the documentation and tracking of root cause analyses and CAPA implementation
Training and Onboarding Support:
Coordinate training assignments and maintain training records
Assist in the onboarding process for new employees, including documentation, system access requests, and coordination with client representatives
Vendor Management Support:
Assist in maintaining records related to GxP vendor compliance and qualification requirements
Support the Account Quality Lead in managing quality-related interactions with third-party vendors and consultants
Administrative Support:
Provide general administrative support to the Account Quality Lead and quality team
Assist in preparing for and documenting quality-related meetings and audits
Help organize and maintain quality-related files and records
Required Qualifications
Education:
Bachelor's degree in Quality Management, Life Sciences, or a related field
Additional certifications in Quality Management Systems (e.g., ISO 9001) are advantageous
Experience:
Minimum of 2 years of experience in a quality assurance or administrative role, preferably in a GxP-regulated environment
Familiarity with medical device or pharmaceutical industry regulations is highly desirable
Knowledge and Skills:
Strong understanding of quality management systems and GxP regulations
Proficiency in Microsoft Office Suite, especially Excel, Word, and PowerPoint
Experience with SharePoint or similar document management systems
Excellent organizational and time management skills
Strong attention to detail and accuracy
Ability to work independently and as part of a team
Good written and verbal communication skills in English and German
Personal Attributes:
Proactive and self-motivated
Ability to handle multiple tasks and prioritize effectively
Strong problem-solving skills
Commitment to continuous improvement and quality excellence
Help shape JLL
We look forward to receiving your application, stating your earliest possible starting date and your salary expectations.
Please understand that paper applications cannot be accepted and, due to reasons of data protection, will be destroyed.
Jones Lang LaSalle SE
Your contact:
Stefanie Korte
stefanie.korte@jll.com
Location:
On-site –Norderstedt, SHIf this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table!
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