Senior Visual Inspection & Process Engineer

Lonza; Stein; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile culture

Inclusive workplace

Competitive benefits

Zusammenfassung

Lonza in Stein, AG, Switzerland is seeking a hands-on professional to lead development, qualification, validation and implementation of automated and semi-automated visual inspection and CCIT processes. This site-based role focuses on building robust inspection systems from the ground up with limited guidance.

You will work on qualification, validation, risk analysis, and regulatory readiness, collaborating across teams to ensure product quality and compliance in a growing Drug Product

Qualifikationen

• Proven hands-on experience in pharmaceutical visual inspection for drug products in vials or syringes across manual, semi-automated, or fully automated systems.
• Knowledge of qualification of visual inspection machines and product validation; CCIT experience preferred.
• Ability to work independently in a dynamic environment, building processes and standards from the ground up.

Aufgaben

• Support production staff on the shopfloor with scientific expertise.
• Support GMP-compliant qualification and validation activities of visual inspection systems.
• Prepare readiness for takeover of automated, semi-automated, and manual visual inspection and CCIT testing.
• Ensure safety, compliance and regulatory aspects; prepare risk analyses and relevant procedures.
• Drive technical improvements and troubleshoot processes.
• Lead/participate in change controls and deviations using data to identify root causes.
• Represent VI and CCIT during regulatory inspections and audits.

Kenntnisse

Visual inspection expertise

CCIT knowledge

Process improvement mindset

Independent work

GMP knowledge

Ausbildung

Relevant scientific or engineering degree

Tools

AVI inspection machines

Container Closure Integrity Testing tools

Jobbeschreibung

Lonza in Stein, AG, Switzerland is seeking a hands-on professional to lead development, qualification, validation and implementation of automated and semi-automated visual inspection and CCIT processes. This site-based role focuses on building robust inspection systems from the ground up with limited guidance.

You will work on qualification, validation, risk analysis, and regulatory readiness, collaborating across teams to ensure product quality and compliance in a growing Drug Product