Job Description:
Join QPS Engineering AG as a Project Engineer / CQV Engineer (Pharma) and 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
About QPS Engineering AG
QPS Engineering AG is a dynamic and growing engineering firm providing complete project management, qualification, and validation services, particularly within the pharmaceutical sector. We work according to GMP regulations and support our clients from FAT/SAT through to validation processes. Join us and contribute to impactful pharmaceutical projects in a supportive and innovative environment.
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
- An inclusive and 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).
