Job Description:
Join QPS Engineering AG as a Senior CQV Engineer / CQV Lead and 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
Location: Stein, Aargau, Switzerland
Type: Full-time, Hybrid
Company: QPS Engineering AG
Experience: Minimum 4 years
About QPS Engineering AG
QPS Engineering AG is a dynamic and growing engineering firm providing complete project management, qualification, and validation services, with a focus on the pharmaceutical sector. We operate under 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 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.
Benefits:
- Competitive salary
- 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).
