QC Biochemical Technician
Italy - Monza Update time: May 4,2020
Job Description

Monza site is a world class contract manufacturing facility, specialized in aseptic injectable drugs, with an increasing focus on biologics. Joining more than 1000 colleagues on site, the selected candidate will experience a smart, driven, and fast-growing environment. With revenues of more than $25 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

You will be part of a dedicated team of professionals with a strong biochemical expertise, focused on large molecules products. Working with state-of-the-art products and technologies, you will perform critical analysis in a GMP environment, supporting the introduction of new products, technology transfer, and commercial production.

Key tasks

  • Perform chemical and biochemical analysis of raw materials and finished products in accordance with the cGMP, and communicating in a timely manner to the supervisor any anomalies;
  • Perform validation, verification and transfer activities to support the project;
  • review of documentation and laboratory records;
  • Operate on a wide variety of techniques (ELISA, SDS page, Western Blot, IEF, ..) with the possibility to gain expertise on chemical techniques (HPLC).
  • Generate valid data, report results on appropriate database compared to established specifications while adhering to GMPs.
  • Maintain equipment and troubleshoots instrumentation problems, procedural problems or production problems.
  • Observe laboratory schedules to accomplish a high volume of critical work without compromising the integrity of the results while meeting the scheduling needs of manufacturing.
This role is the perfect opportunity for a QC technician with biochemical expertise to join a dynamic team, with a strong exposure to international clients, and a commitment to excellence.

Qualification
  • MsC or PhD in Biochemistry, CTF, or similar fields
  • At least 2-3 years of experience as analyst in a GMP manufacturing facility;
  • Good expertise in Biochemical analysis (ELISA, SDS page, Western Blot, IEF). First-hand experience with vaccines is strongly preferred.
  • Knowledge of Chemical analyses (HPLC, ICP; HVLD) is a preferred;
  • Good Italian and English Level (written and spoken)

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