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

Full-Time; Germany (OH); Hybrid; USD 70,000 - 110,000; Full time

Benefits offered by this job

Company pension scheme

Success participation

Provision of a cell phone

Regular team events

Mentoring program

30 days of vacation

Job summary

A leading consulting firm in life sciences is seeking a qualified professional to manage qualification projects. You will be responsible for planning, documentation, and execution of these projects while collaborating closely with clients. Candidates should possess a degree in pharmaceutical engineering and have extensive experience in GMP environments. Excellent communication skills in German and English are required, along with proficiency in MS Office. The position offers flexible hours and a stable environment within the life sciences sector.

Qualifications

• Extensive experience in GMP qualification/GMP environment.
• Curiosity and motivation to make things better.
• Quick grasp of complex topics.
• Excellent written and spoken German and English
• Proficient in MS Office (Word)
• Team player with strong communication skills and a passion for working with clients

Responsibilities

• Self-responsible planning and implementation of qualification projects.
• Creation and maintenance of relevant documents.
• Coordination and execution of qualification activities.

Skills

Strong organizational skills

Excellent written and spoken German

Excellent written and spoken English

Proficient in MS Office

Team player with strong communication skills

Education

Degree in pharmaceutical engineering or related field

Chemical engineering degree

Process engineering degree

Biotechnology degree

Tools

MS Office (Word)

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

• Self-responsible 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)
• Coordination and 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)
• Extensive experience in GMP qualification / GMP environment
• 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

Flexible working hours tailored to your projects and personal needs.

Company pension scheme

Allowance to your direct insurance.

Success participation

Attractive compensation including sucess-sharing.

Provision of a cell phone upon joining the company.

Crisis-proof workplace

Permanent employment contract in the stable life sciences sector.

Team-events

Regular team events to switch off together.

Development

Mentoring program and opportunities for 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!