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Software Engineer (Pharma)

QPS Engineering AG -
Stein, AG

Jetzt bewerben

Details zur Stelle

Festanstellung | 100% | Pensum: 90-100%

Qualifikationen

C#
Englisch
.NET
Master
SQL
Bachelor
JavaScript
Softwareentwicklung
Erfahrung in der IT
Produktion
Python
Deutsch

Vollständige Stellenbeschreibung

Job Description:

Join QPS Engineering AG as a Software Engineer (Pharma)

Become part of a future-oriented team driving digital innovation in pharmaceutical manufacturing. In this role, you will design, implement, and validate software systems that support GMP-compliant production processes, ensuring data integrity, system reliability, and regulatory compliance.

You’ll work on high-impact projects in close collaboration with cross-functional teams and bring your technical expertise to the core of pharmaceutical digitalization. If you are passionate about software engineering and have at least 2 years of experience in the field, we look forward to your application!

Job Title:
Software 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’ll play a key role in shaping the digital future of pharmaceutical operations. We value innovation, interdisciplinary teamwork, and technical precision.

You’ll work alongside passionate professionals on meaningful projects that directly contribute to patient safety and product quality.

Benefits

Competitive salary
Opportunities for professional development and certifications
Hybrid work model
A supportive and inclusive work culture

Responsibilities:

Designing, developing, and integrating software systems for GMP-regulated production environments
Supporting the creation of system specifications, user requirement specifications (URS), and functional design specifications (FDS)
Implementing and validating software solutions such as MES, LIMS, SCADA interfaces, and database applications
Ensuring compliance with GAMP 5, 21 CFR Part 11, EU Annex 11, and other pharmaceutical software validation standards
Collaborating with cross-functional teams to define and execute qualification and validation strategies (IQ/OQ/PQ)
Managing risk assessments related to software systems, including cybersecurity and data integrity topics
Providing internal training and documentation on validated software applications

Preferred Qualifications:

Bachelor’s or Master’s degree in Computer Science, Software Engineering, or a related technical field
Minimum of 2 years of experience in software development or integration within the pharmaceutical, biotech, or life sciences sector
Strong knowledge of GMP, GAMP 5, and regulatory requirements for computerized systems
Hands-on experience with languages and technologies such as Python, C#, .NET, SQL, JavaScript, or modern web frameworks
Familiarity with manufacturing IT/OT systems (e.g., MES, LIMS, SCADA, ERP integrations)
Fluent in German and English (written and spoken)
Excellent analytical thinking and structured approach to software lifecycle documentation

Full time / Hybrid

Stein, Aargau, Switzerland

permanent position

Join Our Team!

- Exciting projects
- Professional growth
- Collaborative team

Shape the future with us. Apply today!

Jetzt bewerben

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