Join QPS Engineering AG as a Senior CQV Engineer / CQV Lead Be part of a dynamic team leading the future of pharmaceutical engineering. In this role, you will manage the implementation and validation of critical systems in pharmaceutical production, ensuring compliance with GMP and CQV standards.
This position offers a unique opportunity to work on high-impact projects, collaborate across teams, and help maintain the highest quality and safety standards for pharmaceutical products. If you have a passion for CQV and at least 4 years of experience, we’d love to hear from you!
Job Title:
Senior CQV Engineer / CQV Lead
Type:
Full-time, Hybrid
Experience:
Minimum 4 years
What We Offer At QPS Engineering AG, you will have the chance to make a meaningful contribution to the success of a growing company. We provide a collaborative and innovative work environment where your ideas and skills 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
An inclusive and supportive team culture
Responsibilities
Leading, planning, executing, and documenting qualification and validation activities for pharmaceutical systems and processes.
Supporting the development of system and process specifications.
Collaborating with multidisciplinary teams to ensure CQV procedures are followed and standards are met.
Identifying and managing risks to ensure safety, quality, and efficiency in production.
Conducting training sessions and presentations on CQV topics for relevant personnel.
Preferred Qualifications
Bachelor’s or Master’s degree in Chemical Engineering, Bio-process Engineering, or a related technical field.
Minimum of 4 years of experience in a similar role within the pharmaceutical or biotechnology sector.
Strong knowledge of
GMP ,
CQV , and pharmaceutical regulatory requirements.
Excellent problem-solving skills and strong attention to detail.
Fluency in
German
and
English
(written and spoken).
#J-18808-Ljbffr
This position offers a unique opportunity to work on high-impact projects, collaborate across teams, and help maintain the highest quality and safety standards for pharmaceutical products. If you have a passion for CQV and at least 4 years of experience, we’d love to hear from you!
Job Title:
Senior CQV Engineer / CQV Lead
Type:
Full-time, Hybrid
Experience:
Minimum 4 years
What We Offer At QPS Engineering AG, you will have the chance to make a meaningful contribution to the success of a growing company. We provide a collaborative and innovative work environment where your ideas and skills 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
An inclusive and supportive team culture
Responsibilities
Leading, planning, executing, and documenting qualification and validation activities for pharmaceutical systems and processes.
Supporting the development of system and process specifications.
Collaborating with multidisciplinary teams to ensure CQV procedures are followed and standards are met.
Identifying and managing risks to ensure safety, quality, and efficiency in production.
Conducting training sessions and presentations on CQV topics for relevant personnel.
Preferred Qualifications
Bachelor’s or Master’s degree in Chemical Engineering, Bio-process Engineering, or a related technical field.
Minimum of 4 years of experience in a similar role within the pharmaceutical or biotechnology sector.
Strong knowledge of
GMP ,
CQV , and pharmaceutical regulatory requirements.
Excellent problem-solving skills and strong attention to detail.
Fluency in
German
and
English
(written and spoken).
#J-18808-Ljbffr
Senior CQV Engineer / CQV Lead (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.
