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!
Type:
Full-time, Hybrid
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.
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).
#J-18808-Ljbffr
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!
Type:
Full-time, Hybrid
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.
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).
#J-18808-Ljbffr
Project Engineer / CQV Engineer (Pharma) Arbeitgeber: QPS Engineering AG
QPS Engineering AG ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, in einem innovativen und kollaborativen Umfeld zu arbeiten, das sich auf die Zukunft der pharmazeutischen Technik konzentriert. Mit einem starken Fokus auf berufliche Weiterentwicklung und einer unterstützenden Teamkultur können Sie an bedeutenden Projekten mitwirken und Ihre Ideen einbringen, während Sie gleichzeitig von flexiblen Arbeitsmodellen profitieren.
