Join Lonza, a global leader in life sciences, and contribute to impactful pharmaceutical projects. We are seeking a CSV Engineer to support the commissioning, qualification, and validation (CQV) activities of cutting-edge systems in Stein, Switzerland.
Responsibilities
Oversee and execute CSV deliverables and tests for Delta V software development, ensuring compliance with Lonza SOPs and regulatory guidelines.
Develop, review, and manage CSV documentation throughout the project lifecycle.
Serve as the subject matter expert (SME) for CSV activities, ensuring alignment with Lonza's CQV standards.
Collaborate with cross-functional teams, including Process Engineers, QA, Automation, and Project Managers, to deliver successful outcomes.
Execute validation testing (FAT/SAT) and ensure seamless integration of systems into the Lonza environment.
Provide technical expertise, address compliance gaps, and support inspections as the CSV representative.
Join Lonza, a global leader in life sciences, and contribute to impactful pharmaceutical projects. We are seeking a CSV Engineer to support the commissioning, qualification, and validation (CQV) activities of cutting-edge systems in Stein, Switzerland.
Responsibilities
Oversee and execute CSV deliverables and tests for Delta V software development, ensuring compliance with Lonza SOPs and regulatory guidelines.
Develop, review, and manage CSV documentation throughout the project lifecycle.
Serve as the subject matter expert (SME) for CSV activities, ensuring alignment with Lonza's CQV standards.
Collaborate with cross-functional teams, including Process Engineers, QA, Automation, and Project Managers, to deliver successful outcomes.
Execute validation testing (FAT/SAT) and ensure seamless integration of systems into the Lonza environment.
Provide technical expertise, address compliance gaps, and support inspections as the CSV representative.
qualifications
Requirements
Bachelor's degree in Engineering, Applied Sciences, or a related technical field.
Minimum of 5 years in CSV/CQV, with expertise in Delta V DCS and large pharmaceutical projects.
Familiarity with regulated environments (EMA/FDA) and experience in biologics or chemical manufacturing.
Proficiency in ISPE GAMP5 and ASTM guidelines.
Hands-on experience in vertical integration, data management, and validation testing (FAT/SAT).
Strong analytical and organizational abilities with a proactive, solution-driven mindset.
Fluent English is mandatory; German is an advantage.
Take this opportunity to join Lonza and make a difference in the life sciences industry!
Apply now and shape the future with Lonza.
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informations de contact.
nous sommes à ta disposition pour toute question.
RA
Rodin Ak
Randstad Lonza Visp
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