This is a unique chance to work with qualification and documentation in building and equipment investment projects ranging from small to large investments (several million Euros). The product classes range from animal feed through foodstuff, to pharma and infant formula.
You will join an agile team of 5 skilled and dedicated colleagues working across the global Chr. Hansen organization. We work with many exciting projects in a very dynamic environment where we can see and feel the results of our work. Even though we are busy, we always have time to help and share knowledge. We work as a team, we win as a team and we celebrate as a team.
Working as Quality Engineer you must thrive in a dynamic setup where your experience and personality help you deliver professional and effective results. This includes the ability to plan and prioritize the work and keep an overview of the processes.
You will be working across all engineering disciplines. This takes good people skills and communication skills in English, written and spoken. As such, you can transmit your personal enthusiasm and quality mindset to other people around you and ensure deliveries according to plans and deadlines.
Your primary tasks, within areas of responsibility, will be:
- Review of User Requirement Specifications URS, FAT, SAT, IQ, OQ protocols and test plans
- Support engineering package owners in structuring deliverables according to Validation Master Plan
- Maintain relevant SOPs and Forms in the Quality Management System (QMS)
- Support preparation of internal and external audits
- Train others in good documentation practice
- Maintain training plans
- Review of qualification test results and deviations
- Participate in audits/inspections on site and assist at audits of external partners
You will be based at our Avedoere site in the Copenhagen area, but you can expect to be located at our sites in Roskilde and Hoersholm while participating in projects.
You come with an educational background from engineering or life science and are comfortable to set the Quality direction in collaboration with stakeholders.
You must have relevant GMP equipment qualification and validation experience (min 2 years) and capabilities to ensure compliance with our internal SOPs. Gathering, reviewing and organizing critical documentation across several work packages will be your primary tasks.
For more information and application
If you have any questions about the position, please feel free to contact Ole Hoejgaard, Team Manager, Team Q on email@example.com.
Deadline for applications is April 28th 2019.
Please write in your application that you've seen the job at Jobfinder.