Quality Control Analyst (Shift work) (m/f/d) in Monteggio

Mari Slavova, Randstad Inhouse Services Lonza Visp
jetzt bewerben

job details

Monteggio, Tessin
Life Sciences
Mari Slavova, Randstad Inhouse Services Lonza Visp
+41 61 316 25 42


We are looking for a Quality Control Analyst(m/f/d) for Lonza AG (100%). This is a temporary position until 31.10.2022. The position includes shift work (morning, afternoon, night).

Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of.

Key responsibilities

· Identification and characterization of the. incoming materials and products (FT-IR, Microscope)

· IPCs and release analyses (PSD- Karl Fischer)

· Check of the cleaning status of production equipment and micronization room, through visual inspection and swab test

· Check and registration of the results according to the current SOPs, cGMPs

· Timely communication related to deviations from standards and OOS, OOT, OOE management according to the current SOP and in cooperation with all the involved departments

· Preventive maintenance of the laboratory instruments

· Solvents and reagents management

· Ordinary cleaning of the laboratory and related instrumentation

· Management of the archive samples

· Management of the disposal activities related to the material coming from the laboratory in cooperation with the warehouse department

· Collaboration in drafting and reviewing the company documentation such as SOPs, protocols and reports


  • University degree in the science field preferred
  • Work experience in cGMP Operations- QC
  • Able to relate to coworkers
  • Solving problem ability
  • Understanding of technical and scientific data
  • Professional, analytical and patient
  • Knowledge and understanding of GMP principles, industry practices, and standards with demonstrated ability to apply these to daily operations.
  • Strong attention to detail with strong documentation and coordination practices.
  • Fluent Italian and good English skills