Internship MSAT Upstream 80-100%

The internship is offered by Lonza at its Visp site in Switzerland. In this position you will support Process Experts and Senior Process Experts who work on large‑scale mammalian upstream and downstream production of biopharmaceuticals. The role is fully on‑site for a twelve‑month period, providing hands‑on experience in a regulated manufacturing environment. Your daily tasks will involve helping with technology transfer by drafting and organizing process paperwork, gathering and analysing batch data, and tracking performance trends. You will also assist in creating presentations and reports for internal teams and customers, take part in risk assessments, change‑control activities, and continuous‑improvement projects. Collaboration with Manufacturing, MSAT, QA, and Process Development groups will be required, as will maintaining GMP‑aligned documentation and ensuring data integrity. Participation in team meetings, note‑taking, and follow‑up on actions will also be part of the routine. The internship requires that you are currently pursuing or have finished a Bachelor's or Master's programme, or hold equivalent experience, in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or a closely related discipline. You should show a strong interest in biopharma manufacturing and process science, possess solid English communication abilities, and be organized, detail‑oriented, and able to work well within a team. The environment is fast‑moving, so adaptability and comfort with a dynamic pace are essential. Lonza promotes an agile career path, an inclusive culture, and performance‑based compensation, with benefits that vary by role and location. The Visp location offers direct, in‑person collaboration that enhances technical precision. German language skills are advantageous but not mandatory, and a basic grasp of bioprocessing and GMP practices is considered a plus. What the role asks for: - Bachelor's or Master's degree (or equivalent) in relevant science field - Strong interest in biopharma manufacturing and process science - Excellent English communication skills - Organized, detail‑oriented team player - Comfortable in a fast‑paced, dynamic setting - Basic understanding of bioprocessing and GMP (nice‑to‑have) - German language ability (nice‑to‑have)