Join Lonza's growing Biologics organization in Visp and play a key role in ensuring the highest standards of equipment cleaning and contamination control for innovative bioconjugate manufacturing processes. This is an opportunity to contribute to the production of life-changing therapies while driving operational excellence and continuous improvement. The role is fully site-based in Visp, Switzerland, supporting close, real-time collaboration and technical precision needed to manufacture medicines to the highest quality and safety standards. Relocation assistance is available for eligible candidates and their families, if needed.
Tasks
- Lead and coordinate GMP investigations related to cleaning.
- Own end-to-end cleaning deviation management, including investigation, root cause analysis, impact assessment, documentation, and timely closure, while driving CAPAs and continuous improvements to enhance process robustness and operational performance.
- Review manufacturing data, electronic batch records, process parameters, equipment logs, and analytical results to support deviation investigations and product impact assessments.
- Collaborate with cross-functional teams including Manufacturing, Quality Assurance, MSAT, Engineering, Validation, and QC to resolve complex operational and GMP issues.
- Support regulatory inspections, customer audits, and internal audits by presenting investigation outcomes, CAPA strategies, and quality system effectiveness.
- Provide coaching and guidance to manufacturing personnel on deviation reporting, investigation practices, GMP documentation, and quality culture.
- Contribute to process monitoring, risk management activities, and operational excellence projects to improve compliance, productivity, and process reliability.
Requirements
- Degree in Biotechnology, Biochemistry, Biochemical Engineering, Life Sciences, or a related scientific discipline (Bachelor's, Master's, or PhD).
- Experience in biopharmaceutical, biotechnology, or GMP-regulated manufacturing environments, particularly in upstream or downstream processing.
- Understanding of equipment cleaning, cleaning validation, contamination control, or related process engineering activities.
- Knowledge of GMP requirements, quality systems, and manufacturing documentation practices.
- Familiarity with USP/DSP equipment and process equipment design within biotechnology production environments.
- Strong communication and collaboration skills, with the ability to work effectively across multiple functions and stakeholders.
- A structured, solution-oriented mindset with a passion for continuous improvement, learning, and driving operational excellence.
Benefits
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Compensation programs that recognize high performance.
- A variety of benefits dependent on role and location.
- Relocation assistance for eligible candidates and their families, if needed.
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