Can you bridge QA and IT and secure an easy-to-go user interface?
If your background comprises a solid understanding of QA and good overall IT-competencies we have just the perfect job waiting for you. In a newly established position you will become the key person in our efforts to ensure optimally accessible and up-to-date QA documents across the global organization. You can look forward to joining a very successful and market leading, global company in a job with ample opportunities for influence, impact and development.
Optimize our global Quality Management Systems and deliver user support
You will unfold your skills across two main tasks founded within our global Quality Management Systems (QMS). One focus area is to optimize and support the use of our QMS including our very important core Standard Operating Procedures (SOP’s) - we call it House of Quality (HOQ). In this you will be trusted to re-think/optimize the overall system architecture in order to ensure easy and logical access as well as easy-understandable content. Your other focus area is to support the validated IT systems owned by QA (primarily SharePoint but also SAP). This includes document control, deviations and change control.
In overview you will:
- Create a new structure of our QMS and HOQ to ensure easy and logical access - system architecture
- Perform daily system ownership and ensure that the agreed system governance process and changes are implemented as planned
- Provide user support for application and user-related user requests, QA-documents
- Optimize content of SOP’s to ensure best possible understanding - with help from our global subject matter experts
- Coordinate annual plan of expected changes in SOP’s
- Secure focus and progress on IT-related tasks solved by IT or external partners
Across your tasks you will follow the relevant requirements of FDA FSMA, EU GMP and ISO22000 to ensure we always are in compliance with authority regulations. As your focus is QA documents and systems related to those, more hardcore IT-related user requests are solved by IT.
Good understanding of QA and related IT systems
There is no “right” education for this unique job. We imagine that you have a background in QA and additional skills within IT - optimally SharePoint and SAP. As such, you have knowledge of the regulations linked to food and pharma production – solid GMP understanding. This includes validation of IT systems according to EU/FDA requirements as well as GAMP5 and Part11. You also know ISO22000. In total, you can create the right overall architecture and support the users.
You will naturally need all of your ability to systemize, structure and build a logical and user-friendly framework. As you will support multiple colleagues across the global organization you must thrive on contact to other people and at the same time possess the necessary patience to guide in a service oriented and positive way. Finally, you must have a strong command of English, written and spoken.
Your new team
You will join a small and agile team of 3 experienced and skilled QA Professionals spanning QA & IT. We work in an informal atmosphere characterized by a good and open dialogue. We believe that the best results are created in an environment of honesty and mutual trust with plenty of room for humor and common laughs.
If you have any questions about the position, please feel free to contact Senior Quality Systems Manager Flemming Hawthorn Jensen at +45 5339 4085.
Please apply on-line. Here you can enter your details into our CV-bank. Deadline for applications is 28 August 2017.
Read more about working for Chr. Hansen at: www.chr-hansen.com/career
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