Senior Process Expert - Visual Inspection 80-100%

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

Switzerland, Stein

The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. You will lead the development, qualification, validation, and implementation of automated and semi-automated inspection and container closure integrity testing processes, ensuring robust defect detection and product quality from the ground up. This is a unique opportunity for someone who thrives in a pioneering environment, enjoys building processes from scratch with limited guidance, and wants to help shape the future of a growing Drug Product manufacturing site. Check out Your Career in Drug Product Services at Lonza! This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What You Will Get

• An agile career and a dynamic work culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits

What You Will Do

• S upport the production staff on the shopfloor by providing scientific expertise
• Support the GMP compliant qualification and validation activities of automated visual inspection system from an Operations perspective
• Prepare readiness for operative takeover of the automated, semi-automated, manual visual inspection and container closure integrity testing
• Accountable for safety, compliance and regulatory aspects. Preparation of risk analysis and all relevant procedures to ensure regulatory compliance and achieve business goals.
• Technical improvement execution: Execute improvements, Drive process related trouble shooting
• Leading/participate in change controls and deviations: using scientific and statistical knowledge to analyze data to provide process understanding, and to identify root causes of product and process failures.
• Represent the VI and CCIT during regulatory inspections and audits.

What We Are Looking For

• Proven hands‑on experience in pharmaceutical visual inspection for drug product in vials or syringes, in EITHER manual visual inspection, semi-automated, and/or fully automated visual inspection machines (AVI); experience across multiple inspection technologies is highly preferred.
• Knowledge of qualification of visual inspection machines, product validation and ideally with Container Closure Integrity Testing (CCIT) is preferred.
• Ability to work independently in a dynamic environment, building processes, standards, and solutions from the ground up with limited guidance and a strong continuous improvement mindset.
• Fluent in EITHER English OR German is required (fluency in both languages is an advantage)
• A relevant scientific or engineering degree is preferred, although equivalent technical training combined with substantial industry experience will also be considered.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Reference: R77569

Apply