Process & Cleaning Specialist

for the site Borgo San Michele LT, 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. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.

Process & Cleaning Specialist

for the site Borgo San Michele LT, 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. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.

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.

Your motivation

Are you looking for new challenges in a highly competitive environment? And you want to tackle them creatively and on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions rather than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!

If you have any questions, I - Chiara Fanasca / Human Resources - will be happy to help you: +393884526179