Biotechnologist Drug Product 80-100% (m/f/d)
Role overview
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
## Mansioni - Carry out end‑to‑end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results. - Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities. - Ensure every batch is made safely, on time, and according to quality and aseptic standards. - Set up, operate, and clean equipment for liquid and freeze‑dried (lyophilized) vial manufacturing. - Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection. - Train colleagues and support cross‑functional teams with technical guidance. - Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.
## Requisiti - 2–4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish). - Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles. - Good English skills for instructions and communication; German is a plus. - Familiarity with GMP, SOPs, and quality processes. - Reliable, well‑organized, team‑oriented working style. - IT knowledge (SAP/MES is a plus). - Willingness to support on‑call duties to some extent. - Currently operating in a 2‑shift system; readiness for 3‑shift work (regular 5‑day week, occasional Saturday, no Sundays).
Description
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
## Mansioni - Carry out end‑to‑end Drug Product manufacturing under GMP: batch execution, documentation, troubleshooting, and review of results. - Complete and maintain all GMP documentation (batch records, logbooks, forms). Support process changes and CAPA activities. - Ensure every batch is made safely, on time, and according to quality and aseptic standards. - Set up, operate, and clean equipment for liquid and freeze‑dried (lyophilized) vial manufacturing. - Support compounding & formulations, buffer preparation, washing/autoclaving, filter integrity testing, filling/crimping, and visual inspection. - Train colleagues and support cross‑functional teams with technical guidance. - Report equipment issues and support engineering teams with repairs in cleanroom/aseptic areas.
## Requisiti - 2–4 years of GMP shopfloor experience (ideally sterile Drug Product / Fill & Finish). - Drug Product experience is a strong advantage. EFZ apprenticeship (mechanic or similar: production mechanic, car mechanic, etc.) Also practical experience in professions with high hygiene and cleanliness requirements, such as cook/chef or comparable roles. - Good English skills for instructions and communication; German is a plus. - Familiarity with GMP, SOPs, and quality processes. - Reliable, well‑organized, team‑oriented working style. - IT knowledge (SAP/MES is a plus). - Willingness to support on‑call duties to some extent. - Currently operating in a 2‑shift system; readiness for 3‑shift work (regular 5‑day week, occasional Saturday, no Sundays).
