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Full-time
bachelor degree
Lifestyle Benefits, Family Benefits, Leisure Benefits, Performance Recognition Programs
Posted 34d ago
~40 hrs/week
Responsibilities
Lead the development, qualification, and implementation of automated and semi-automated visual inspection and container closure integrity testing processes. Provide scientific expertise to production staff and ensure regulatory compliance through risk analysis and deviation management.
Requirements
Requires proven hands-on experience in pharmaceutical visual inspection for vials or syringes and knowledge of machine qualification. A scientific or engineering degree is preferred, along with fluency in English or German.
Full job description
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.
Support 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.
Related keywords
Visual InspectionCCITAVIGMPDrug ProductVialsSyringesValidationQualificationPharmaceuticalsRoot Cause AnalysisChange ControlRegulatory ComplianceProcess EngineeringDrug Product Services
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.