Operator Biotechnologist (f/m/d)

Lonza, a worldwide leader in life‑science solutions operating on five continents, is hiring an Operator Biotechnologist for its Visp site in the Swiss canton of Valais. The company emphasizes the power of talented individuals to generate ideas that support businesses and improve lives. Employees are encouraged to shape their own careers, contributing both large and small innovations that have a global impact. This position joins a growing team that supports multiple business units at the Visp facility. The role involves carrying out manufacturing tasks within the drug‑product sector while adhering to current‑good‑manufacturing‑practice (cGMP) standards. Daily duties include executing batch runs, monitoring progress, and addressing any deviations that arise. The operator must perform visual inspections of both liquid and freeze‑dried vials, removing any units that show particles, container defects, or integrity issues, thereby guaranteeing a sterile product suitable for patient injection. Additional responsibilities cover preparing and maintaining production records such as batch manufacturing records and related forms, as well as setting up, operating, and cleaning the equipment and work area as needed. The candidate must have prior experience working in a GMP‑controlled setting, ideally within sterile drug‑product manufacturing. A solid understanding of GMP regulations, quality protocols and standard operating procedures is required. The employer looks for a collaborative attitude, strong teamwork skills and the ability to communicate clearly across different functions. The ideal applicant is organized, detail‑oriented and capable of maintaining focus under pressure, while also demonstrating high motivation, proactivity and dynamism in daily tasks. They must also be prepared to work flexible hours and participate in a two‑shift schedule. A methodical, focused and well‑organized work style is essential for maintaining batch integrity and documentation accuracy. The position is based in Visp, offering relocation support for qualified candidates and their families if required. Lonza promotes an agile career path within an inclusive and ethical environment, providing performance‑based compensation and a range of benefits tailored to the role and location. The team values problem‑solving creativity and encourages employees to contribute ideas that improve global health outcomes. Employees benefit from a dynamic culture that values inclusivity, ethical conduct and continuous professional growth and overall well‑being. What the role asks for: - Experience in a GMP‑regulated environment - Knowledge of GMP requirements, quality procedures and SOPs - Strong team orientation and collaborative mindset - Excellent communication skills - Structured, focused and well‑organized work style - Availability for flexible hours and 2‑shift pattern