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

Full-Time; Deutschland; On-site; EUR 55,000 - 90,000; Full time

Benefits offered by this job

Company pension

Success participation

Cell phone

Permanent contract

Team events

Mentoring program

Vacation 30 days

Job summary

allegra-consulting is seeking a qualified engineer to lead GMP qualification projects at our customers' sites in the life sciences sector.

You will create and maintain user requirement specifications, risk analyses, qualification test specifications, and coordinate qualification activities.

Fluent German (C1) and English (B2), strong organizational skills, teamwork and MS Office proficiency (Word) are essential; we offer flexible hours, a company pension, and a permanent contract.

Qualifications

• Degree in pharmaceutical/chemical/process engineering or biotechnology or an equivalent qualification.
• Extensive GMP qualification / GMP environment experience.
• Excellent German (C1) and English (B2) skills.
• Strong organizational abilities and ability to grasp complex topics.
• Proficient in MS Office, especially Word.

Responsibilities

• Self-responsible planning and implementation of qualification projects at customers' sites
• Creation and maintenance of user requirement specifications, risk analyses, qualification test specifications
• Coordination and execution of qualification activities

Skills

German (C1)

English (B2)

Organizational skills

Teamwork

Client communication

Education

Degree in pharmaceutical engineering

Degree in chemical engineering

Process engineering degree

Biotechnology degree

Certified technician or master craftsman

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 (C1) and English (B2)
• Proficient in MS Office (particularly Word)
• Team player with strong communication skills and a passion for working with clients

Flexible working hours tailored toyour 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 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 yourwell-being.

Become part of our success-story