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QC Analyst; f​/m​/d

Job in 20061, Carugate, Lombardia, Italy
Listing for: Altro
Full Time position
Listed on 2026-07-19
Job specializations:
  • Quality Assurance - QA/QC
  • Pharmaceutical
Salary/Wage Range or Industry Benchmark: 32000 - 46000 EUR Yearly EUR 32000.00 46000.00 YEAR
Job Description & How to Apply Below
Position: QC Analyst (f/m/d)
Location: Carugate

QC Analyst

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 semi solids, these include creams and gels.

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

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

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 (Good Manufacturing Practice) regulations.

Good knowledge of major analytical techniques and laboratory documentation practices.

Member of the Aenova Group

Via delle Industrie 2

20061 Carugate MI, Italy

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