Junior GMP Qualification Engineer Pharma (m/w/d)
Full-Time
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Benefits offered by this job
Job summary
Qualifications
- Degree in pharmaceutical engineering, chemical engineering, or related.
- Strong organizational and communication skills.
- Fluency in German and English is essential.
Responsibilities
- Plan and implement qualification projects at customers' sites.
- Create and maintain relevant qualification documents.
- Execute qualification activities.
Skills
Education
Tools
Job description
About us
allegra-consulting - an employer that inspires you
Since 2009, we have been inspiring our clients in the pharmaceutical, biotechnology, cosmetic and medical technology sectors with tailor-made solutions and in-depth expertise.Not just to meet the highest quality standards, but to implement them professionally and efficiently – always in compliance with industry-specific regulations. In this way, we create real added value for our customers while offering a dynamic, challenging environment for our team.
What sets us apart?
Flat hierarchies, short decision-making paths, maximum flexibility – and an exceptional commitment to quality. Our culture thrives on openness, appreciation, and genuine collaboration. We believe that people can only truly grow in the right environment. That’s why we offer flexible working hours, part-time models, and room for life outside of work.Join us in a future-oriented industry – and in a team that not only welcomes you but moves forward with you.
About the job
Want to make a difference, help shape the future and grow personally?
Then you’ve come to the right place! In the life sciences industry you’ll work in a future-proof environment that truly makes an impact – for you, for others, for tomorrow. What do you need? Curiosity, motivation and a desire to make things better. You’ll learn the rest with us – through real team spirit, close collaboration, and projects that challenge and support you.
Your responsibilities
- Planning and implementation of qualification projects at our customers' sites
- Creation and maintenance of all relevant documents (user requirement specifications, risk analyses, qualification test specifications)
- Execution of qualification activities
Your profile
- Degree in pharmaceutical engineering, chemicalengineering, process engineering, biotechnology or a comparable qualification (e.g., certified technician or master craftsman)
- Strong organizational skills and a quick grasp of complex topics
- Excellent written and spoken German and English
- Proficient in MS Office (particularly Word)
- Team player with strong communication skills and a passion for working with clients
- Initial experience in GMP qualification is a plus
Flexible working hours tailored toyour projects and personal needs.
Allowance to your direct insurance.
Attractive compensation including
success-sharing.
Provision of a cell phone upon joining the company.
Permanent employment contract in thestable life sciences sector.
Regular team events to switch off together.
Mentoring program and opportunitiesfor professional and personal development.
30 days of vacation for your well-being.
Become part of our success-story
Ready to take the next step in your career and grow with us? Seize the moment – we look forward to getting to know you!
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