Skip to main content
Lebenslauf anlegen - Einfache Bewerbung auf tausende Jobs.

New Pharma AG Jobs

Sortieren nach: -

Andere Nutzer suchten auch:

regulatory affairs
pharma assistentin
pharma produktion
pharmaceutique

Job Post Details

Project Engineer / CQV Engineer (Pharma) - job post

QPS Engineering AG
4.2 von 5 Sternen
Schaffhauserstrasse 30, Stein, AG
Festanstellung, 100%, Pensum: 90-100%
Erstellen Sie ein Indeed-Konto, bevor Sie zur Website des Unternehmens weitergeleitet werden.

Stellenbeschreibung

Anstellungsart

  • Pensum: 90-100%
  • Festanstellung
  • 100%

Arbeitsort

Schaffhauserstrasse 30, Stein, AG

Vollständige Stellenbeschreibung

Job Description:

Join QPS Engineering AG as a Project Engineer / CQV Engineer (Pharma)

Become part of an innovative team shaping the future of pharmaceutical engineering. You will lead the implementation and validation of critical systems in pharmaceutical production, ensuring compliance with GMP and CQV standards.

This role offers an exciting opportunity to work on high-impact projects, collaborating with multidisciplinary teams and contributing to the safety and quality of pharmaceutical products. If you have a passion for engineering and at least 2 years of experience in the field, we’d love to hear from you!

Job Title:
Project Engineer (Pharma) / CQV Engineer (Pharma)

Location:
Stein, Aargau, Switzerland

Type:
Full-time, Hybrid

Company:
QPS Engineering AG

Experience:
Minimum 2 years

What We Offer

At QPS Engineering AG, you will have the opportunity to contribute significantly to the success of a growing company. We offer a collaborative and innovative work environment where your ideas and expertise will shape impactful pharmaceutical projects.

Our team is highly motivated and eager to welcome new talent who share our commitment to excellence.

Benefits

  • Competitive salary
  • Professional growth opportunities
  • Hybrid work environment
  • Supportive team culture

Responsibilities:

  • Planning, executing, and documenting qualification and validation activities for pharmaceutical equipment and processes.
  • Supporting the creation of detailed system and process specifications.
  • Collaborating across multidisciplinary teams to ensure compliance with CQV protocols and GMP standards.
  • Managing risks to ensure safety, efficiency, and product quality.
  • Conducting training and presentations to internal teams on CQV-related processes.

Preferred Qualifications:

  • Bachelor's or Master's degree in Chemical Engineering, Bio-process Engineering, or a related technical field.
  • Minimum of 2 years of experience in a similar role within the pharmaceutical or biotechnology sector.
  • Proven experience with GMP, CQV (Commissioning, Qualification, and Validation), and pharmaceutical regulatory requirements.
  • Excellent problem-solving skills and a strong attention to detail.
  • Fluent in German and English (written and spoken).
Full time / Hybrid
Stein, Aargau, Switzerland
permanent position
Join Our Team!
    • Exciting projects
    • Professional growth
    • Collaborative team

Shape the future with us. Apply today!

Erhöhen Sie die Chance auf Ihren TraumjobLaden Sie Ihren Lebenslauf hoch