Qualification engineer (m/f/d)
This job posting was automatically translated using AI.
Would you like to contribute your expertise in a new working environment? Then you've come to the right place! We are more than just recruiters - we are your personal career counsellor. Our focus: your next professional step, where you really feel at home.
For our client, a globally active company in the research-based pharmaceutical industry in Oranienburg, we are looking for you as a Qualification Engineer (m/f/d) as part of a temporary employment contract with an option to be taken on.
.What we offer
- Company pension scheme with attractive employer contributions
- Modernly equipped workplaces in innovation centres
- Multiple training opportunities for your career
- Flexible working time models for a better work-life balance
- Subsidised canteen with healthy food options
- Discounted memberships to regional gyms
- Regular team events to strengthen your team
- Subsidised canteen with healthy food options
- Regular team events tobalance
- subsidised canteen with healthy food
- discounted memberships to regional gyms
- regular team events to strengthen team spirit
What you can always rely on at persona service:
- Intensive preparation for the interview with our client
- €50 per month as a gift for your mobility depending on the position, e.g. for a ticket to Germany and other benefits. e.g. for the Germany ticket and much more
- Bonuses as well as holiday and Christmas bonuses and attractive industry bonuses
- Free tutoring for your children on the Ubimaster learning and tutoring platform
- Numerous shopping discounts with well-known brands via our corporate benefits programme
- Excellent personal support and regular feedback meetings
- Multiple further training opportunities
Apply now via WhatsApp
Click here!Job description
- You will be responsible for independently managing and ensuring the GMP-compliant qualification of all equipment, rooms and technical systems in accordance with the applicable national and European guidelines
- In addition, you will be responsible for the professional review, continuous updating and final approval of relevant qualification documents and validation master plans, taking into account internal SOP specifications
- Furthermore, you will be responsible for process-related assurance, that only fully qualified and functional systems and equipment for the manufacture of pharmaceutical products are used at the site
- Your tasks also include defining and strategically developing site-related qualification standards according to the current state of the art and providing technical advice to the neighbouring specialist departments
- As part of your work, you will support the coaching of employees on GMP-compliant documentation and prepare and implement GMPcompliant documentation and create and maintain precise work instructions to ensure high quality standards
- In addition, you will actively support site-wide projects and PQR assessments and carry out the technical assessment of changes, which have a direct impact on the qualification status
- Finally, you are responsible for the technical lead function for qualifications and ensure compliance with global regulations on data integrity within the assigned areas of responsibility at the site
Requirements
- You have successfully completed a degree in natural sciences with a Master of Science, Master of Engineering or Master of Pharmacy
- In addition, you have sound professional experience in the technical qualification of complex plants and systems within a highly regulated environment of modern pharmaceutical manufacturing
- You have a sound knowledge of the applicable GMP regulations and the specific requirements for data integrity.regulations and the specific requirements for data integrity make you particularly suitable for this responsible interface function
- You have a native level of written and spoken German and a good command of English, which you can use confidently for specialist documentation and communication
- In addition, you have a high level of organisational skills and a strong team spirit for successful collaboration with various internal and external specialist departments
- You have a good command of German and a good command of English, which you can use confidently for specialist documentation and communication. cooperation with various internal and external specialist departments
- Finally, you are characterised by your sense of responsibility and work with great initiative and technical interest in new issues of pharmaceutical quality assurance
- In addition to your technical expertise, you will also have a valid work permit and permanent residence in Germany to perform this responsible position
Apply to us now!
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