Open Positions
allegra-consulting – an employer that inspires you
We support varied projects in the pharmaceutical, biotech, cosmetics and medical devices industries with professional competence and thus ensure the implementation of the regulations.
Are you ready for a new challenge in the service industry? Are you a young professional or do you already have professional experience?
Motivation and an innovative service mindset are the basic building blocks you need. A career in the life sciences sector is a crisis-proof job. You will gain a lot of specialist knowledge and experience through exchanges with your colleagues and external partners.
Our company structure is based on mutual appreciation and support within the team. In order to create a pleasant work-life balance, we allow you to work flexibly and offer the opportunity to work part-time.
Do you want to grow with us and be part of our company's success?
Then we look forward to your application.
What we offer:
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Flexible working, flextime, flex days, 30 vacation days, work-life balance
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Performance-related pay
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Further training opportunities, mentoring model, personal responsibility, independent work, “learning by doing”
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Flat hierarchies, open to suggestions for improvement, respectful tone, employee satisfaction
Systematic induction - onboarding
The initial induction takes place through individually tailored induction plans and support from a mentor. You will be introduced to the processes step by step and will also receive support from the entire team at all times.
Varied small to large projects from the entire life sciences industry offer you a high level of experience. Every employee is expected to work independently and responsibly and to continuously optimize processes.
As a technical expert, you will share your knowledge within the projects and/or within the team as well as with customer internal employees. In this way, you benefit from a constant increase in knowledge.
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GMP Qualification Engineer Pharma (m/f/d)The task? You will independently carry out qualification projects directly at the customer's site. You will prepare the necessary documents such as requirement specifications, risk analyses, qualification test specifications and coordinate the implementation of the qualification activities resp. carry them out yourself. Why can you do this? You have a degree in pharmaceutical engineering, chemical engineering, process engineering, biotechnology or similar or training as a master craftsman or technician in comparable disciplines. In addition to good organizational skills and the ability to quickly familiarize yourself with different tasks, you have very good language skills in German and English. You have already become familiar with the use of the PC and the use of relevant work programs (MS Office, focus on MS Word) during your studies or training. You are affable and uncomplicated and enjoy working with customers. Initial knowledge of pharmaceutical quality assurance or the GMP environment is an advantage. What you can't do, we'll teach you. If you have any questions in advance, please call: Anette Fröhlich Phone: +49 170 8047562