Site: Borgo San Michele LT, Italy
Aenova is one of the world's leading contract manufacturers and developers for the pharmaceutical industry, operating 15 sites worldwide with 4,000 employees. Latina is a leading centre of excellence in sterile liquid production and is investing strategically to become a premier European hub.
Your key responsibilities
- Manage and optimize the cleaning processes of production equipment, ensuring compliance with GMP regulations and company procedures.
- Collaborate with manufacturing, quality and engineering teams to develop, validate and monitor cleaning processes (CIP/SIP and manual).
- Draw up and update the technical documentation (SOP, validation protocols, reports) relating to cleaning activities.
- Support investigation activities in case of deviations or non‑conformities related to cleaning processes.
- Participate in the definition and implementation of cleaning validation and cleaning verification strategies.




- Contribute to the continuous improvement of processes through trend analysis and identification of corrective/preventive actions.
- Provide support during internal and external audits (regulatory and clients’) regarding cleaning aspects and related processes.

Your profile
- Degree in Chemistry, Industrial Chemistry, Chemical Engineering, or related scientific disciplines.
- Previous experience (at least 2–3 years) in a similar role in the pharmaceutical or biotechnology sector.
- In-depth knowledge of GMP regulations and EMA/FDA guidelines on cleaning validation.
- Familiarity with the analytical techniques used to verify cleanliness (e.g. TOC, HPLC, visual residues).
- Document management and technical drafting skills in the regulatory field.
- Excellent analytical skills, problem solving and orientation towards continuous improvement.
- Good knowledge of English, written and spoken.
- Aptitude for teamwork and cross‑functional collaboration.
J-18808-Ljbffr

📌 Process & Cleaning Specialist (Italia)
🏢 SwissCo Services AG / Aenova Group
📍 Italia