QC Analyst

12 ago - Carugate
Aenova Group

QC Analyst

Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.
Carugate MI, Italy

Would you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Our site in Carugate is a competence center for semisolids, these include creams and gels.

QC Analyst (f/m/d)
Your key responsibilities

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- Perform analyses of raw materials in accordance with the European Pharmacopoeia (Ph. Eur.) and USP (United States Pharmacopeia).
- Assess the compliance of raw materials with quality specifications and regulatory requirements.
- Perform analytical testing on in-process materials and finished products.
- Operate analytical instruments, including HPLC, GC, UV-Vis spectrophotometers, and IR spectrometers.




- Use laboratory equipment such as pH meters, titrators, and viscometers.
- Perform sampling of process fluids (e.g., purified water and other process waters).
- Record analytical data and test results in compliance with Good Manufacturing Practices (GMP) and Data Integrity principles.
- Ensure compliance with company procedures and the quality standards required by the pharmaceutical industry.

Your profile

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- Chemical Laboratory Technician Diploma or Bachelor’s Degree in Chemistry, Pharmaceutical Chemistry and Technology (CTF), Biotechnology, or a related scientific discipline.
- At least 2 years of experience in a Quality Control laboratory within the pharmaceutical industry.
- Hands‑on experience in the analysis of raw materials according to the European Pharmacopoeia (Ph. Eur.) and/or USP standards.
- Practical experience in the use of HPLC and/or GC instrumentation.
- Knowledge of GMP (Go

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