Project Engineer (m/f/d)

Experteer Italy; Origgio; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An established industry player is looking for a dynamic Project Engineer to join their team in Origgio. This role involves supporting the Project Engineering team in executing both GMP and non-GMP projects, serving as a key contact for suppliers, and managing project activities. The ideal candidate will have a university degree in Industrial Engineering and 3-5 years of experience, preferably in the pharmaceutical sector. If you are proactive, customer-oriented, and have strong project management skills, this could be the perfect opportunity for your career growth.

Competenze

• 3-5 years of experience in project engineering, preferably in pharmaceuticals.
• Knowledge of cGMP, ISO, and safety regulations.

Mansioni

• Support Project Engineering team in executing GMP and non-GMP projects.
• Organize project activities and ensure deadlines are met.

Conoscenze

Project Management

Problem Solving

Communication Skills

Analytical Skills

Customer Orientation

Formazione

University Degree in Industrial Engineering

Strumenti

MS Office (Excel, PowerPoint)

AutoCAD

Descrizione del lavoro

Project Engineer (m/f/d)

We are seeking a Project Engineer for our production plant in Origgio (VA, 30 km from Milan).

If you are a dynamic individual with a problem-solving mindset, interested in working in an international environment and supporting our business growth, this could be the right opportunity for your next career move.

What the job entails

1. Support the Project Engineering team in executing GMP and non-GMP projects from a technical and project management perspective.
2. Serve as a key contact for external suppliers and coordinate with all project team members on-site.
3. Organize and oversee project activities, ensuring all tasks meet deadlines by engaging relevant stakeholders.
4. Participate actively in all project phases as a Project Leader or Team Member, including:
   1. Developing preliminary feasibility studies, basic designs, defining project scope, and estimating timing and costs.
   2. Drafting and reviewing Technical Specifications and URS.
   3. Reviewing offers, participating in negotiations.
   4. Managing orders, maintaining supplier relationships, and controlling costs and deadlines.
   5. Ensuring successful FAT and SAT, and closing punch lists efficiently.
   6. Supporting other functions from qualification to project handover.
5. Build expertise in GMP, EHS norms, regulations, and the pharmaceutical sector.

What you bring

To excel in this role, you should have:

• A university degree in Industrial Engineering (preferably Mechanical).
• Approximately 3-5 years of professional experience in a similar role, preferably in the pharmaceutical sector or related fields.
• Knowledge of cGMP, ISO, and safety regulations.
• Proficiency in MS Office (Excel, PowerPoint) and good knowledge of AutoCAD.
• Fluent English language skills.

Personal attributes and skills

• Strong project management skills.
• Customer-oriented approach.
• Excellent communication skills.
• High analytical and problem-solving abilities.
• Proactive, autonomous, and results-oriented attitude.
• Curious, precise, and passionate about continuous improvement.
• Global perspective and intercultural awareness.
• Ability to work independently and as part of a team.

Location: Origgio (VA)

Grünenthal is an equal opportunity employer. Recruitment will be conducted without regard to religion, gender, sexual orientation, age, origin, disability, or other relevant categories.