Qualification engineer (m/f/d)

This job posting was automatically translated using AI.

Professional
Oranienburg
60,000 - 70,000 € p.a.
Full-time

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

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 now

Do you still have questions?

Your Welcome Team will take care of you!

Call us on +49 2351 7893111.

Ähnliche Stellenangebote

Suitable jobs directly by e-mail

Stay up to date and receive suitable jobs quickly and directly by e-mail.