Engineering Project Manager

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

• Management and supervision of CAPEX investment projects relating to pharmaceutical production plants, including clean rooms, utilities and laboratories
• Planning, budgeting, execution and monitoring of projects in compliance with the timing, budget and quality standards required by the pharmaceutical sector.
• Collaboration with the Corporate functions and internal Quality, Production, MS&T, HSE and Purchasing departments for the definition of the technical and regulatory specifications of the activities for:
  • Feasibility and drafting of the technical solutions to address users’ needDefinition of the budget to be proposed to the different stakeholders
  • Act as project manager of the approved projects;
  • Handover at the end of the works in accordance with company procedures.
• Supervision of the installation, commissioning and start-up phases of the plants and infrastructures.
• Ensure compliance with regulations regarding safety, environment and pharmaceutical quality.
• Participation in defining the investment strategy of the company in the medium to long term.
• Promotion of technological innovation and continuous improvement of productive assets.

Depending on the candidate’s experience, she/he will be integrated into the organization accordingly

Your profile

• Engineering Degree (preferably Mechanical, Chemical, Industrial or similar).
• 4 to 10 years of experience in managing CAPEX projects in the pharmaceutical or life sciences field
• In-depth knowledge of GMP regulations and main regulatory standards (e.g. FDA, EMA).
• Proven experience in managing complex projects in regulated environments.
• Excellent project management, budgeting and supplier management skills.
• Leadership skills, problem solving and working in cross-functional teams.
• Fluent knowledge of English, spoken and written (B2).

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!