Junior GMP Qualification Engineer Pharma (m/w/d)

Full-Time; Deutschland; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Benefits dieser Stelle

30 Tage Urlaub

Betriebliche Altersvorsorge

Diensthandy

Erfolgsbeteiligung

Zusammenfassung

allegra-consulting sucht eine/n qualifizierte/n Ingenieur/in im Bereich Pharma, Chemie oder Prozess, der/die Qualifizierungsprojekte bei Kunden vor Ort betreut. Sie planen, implementieren und dokumentieren Aufträge und arbeiten eng mit Kunden zusammen.

Sie bringen ein relevantes Studium, Organisationsstärke, Deutsch C1 und Englisch B2 sowie MS Office mit. Flexible Arbeitszeiten und eine unbefristete Anstellung unterstützen Ihre Entwicklung.

Qualifikationen

• Abgeschlossenes Studium in einem relevanten Fach.
• Gutes Organisationsvermögen und schnelle Auffassungsgabe.
• Deutsch C1 und Englisch B2 in Wort und Schrift.
• MS Office-Kenntnisse, insbesondere Word.
• Teamplayer mit Kommunikationsstärke und Kundenorientierung.
• Erfahrung in GMP-Qualifikation von Vorteil.

Aufgaben

• Planung und Umsetzung von Qualifikationsprojekten beim Kunden vor Ort.
• Erstellung und Pflege aller relevanten Dokumente (Lasten- und Pflichtenhefte, Risikoanalysen, Qualifikationspläne).
• Durchführung von Qualifizierungsaktivitäten.

Kenntnisse

Organisationsstärke

Teamfähigkeit

Kommunikationsstärke

MS Office (Word)

Gute Deutschkenntnisse (C1) und gute/с

Ausbildung

Abgeschlossenes Studium in pharmazeutischer Ingenieurwissenschaft, Chemieingenieurwesen, Prozessingenieurwesen, Biotechnologie oder vergleichbar

Tools

MS Office

Jobbeschreibung

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 (C1)and English (B2)
• 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.

Company pension scheme

Allowance to your direct insurance.

Success participation

Attractive compensation including
success-sharing.

Provision of a cell phone upon joining the company.

Crisis-proof workplace

Permanent employment contract in thestable life sciences sector.

Team-events

Regular team events to switch off together.

Development

Mentoring program and opportunitiesfor professional and personal development.

Vacation

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!