Lead Engineer Qualification (m/f/d)

Sei unter den ersten Bewerbenden.
Nur für registrierte Mitglieder
Stuttgart
EUR 70.000 - 90.000
Sei unter den ersten Bewerbenden.
Vor 7 Tagen
Jobbeschreibung

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Client: Exyte

Location: Stuttgart, Germany

Job Category: -

EU work permit required: Yes

Job Reference: 7e276fd225b8

Job Views: 1

Posted: 16.05.2025

Expiry Date: 30.06.2025

Job Description:

Your vision is ambitious. Just like ours. Our people are our success. As one of us, you will contribute to engineering excellence for the high-tech markets of the future, including semiconductors, batteries, pharmaceuticals, biotechnology, and data centers. At Exyte, you will be part of a global community of challenge seekers who are ambitious and passionate about innovation. Together, we will build on our company’s long history and keep on leading the way to a better world.

Discover your exciting role

Exyte is a global leader in design, engineering, and delivery of facilities for high-tech industries—serving people and planet through energy-saving and more sustainable engineering.

As Lead Engineer Qualification (m/f/d), you will work in the Bio Life Sciences sector at Exyte Central Europe, reporting to the Group Lead Qualification & Validation. You will collaborate with highly qualified engineers from different regional departments like Stuttgart, Nürnberg, Penzberg, Leverkusen, and work on-site with clients to qualify equipment and facilities. You may also have the opportunity for mobile work, depending on the project.

Responsibilities:

  1. Handle project-specific qualification and validation activities according to GMP regulations.
  2. Prepare and review qualification & validation documents (specifications, risk analysis, plans, reports).
  3. Prepare test protocols for qualification stages (DQ, IQ, OQ, PQ) and oversee their execution.
  4. Coordinate with suppliers and review supplier documentation (FAT/SAT, technical documents).
  5. Communicate between qualification teams, clients, technical engineers, automation, QA, and suppliers; report to CQV manager/project management.
  6. On-site coordination and execution of qualification activities, working under time pressure to drive projects forward.

Qualifications:

  1. Degree in biotechnology, pharmaceutical, process engineering, medical devices, or related fields.
  2. Knowledge of current regulations in qualification and validation (GMP, ISO, 21 CFR, Annex 15, data integrity).
  3. Initial experience in qualification/validation, ideally in the life sciences industry.
  4. Fluent in English; good German skills are required.
  5. Proactive, independent work style with high quality awareness, efficiency, and accuracy.

What we offer:

  1. Two-day onboarding with new colleagues.
  2. Spacious workstations with height-adjustable desks in Stuttgart.
  3. Buddy-System for familiarization with the team.
  4. Possibility of mobile working for work-life balance.
  5. Free coffee and water dispensers.
  6. Subsidized fitness contracts through Egym Wellpass at over 5,000 locations in Germany.

#ExyteCareersAreExciting

Contact and Equal Opportunity:

Exyte is an Equal Employment Opportunity employer committed to diversity and inclusion. We provide equal opportunities regardless of ancestry, gender, sexual orientation, gender identity, race, religion, veteran or disability status, or genetic information.

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