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Engineering Project Manager (m / f / d)

Grünenthal Group

Origgio

In loco

EUR 50.000 - 70.000

Tempo pieno

2 giorni fa
Candidati tra i primi

Descrizione del lavoro

A leading pharmaceutical company in Lombardy is seeking an Engineering Project Manager. The role involves supporting GMP and non-GMP projects, coordinating with suppliers, and managing project activities. The ideal candidate will hold an Engineering degree and have 3-5 years of experience in pharmaceutical manufacturing. Strong project management skills and proficiency in MS Office and AutoCAD are required, alongside business-fluent English. This is a full-time position with significant opportunities for growth.

Competenze

  • 3-5 years of experience in similar roles, preferably in pharmaceutical manufacturing.
  • Knowledge of cGMP, ISO standards, and safety regulations.
  • Business-fluent English skills.

Mansioni

  • Support GMP and non-GMP project execution.
  • Act as key contact for external suppliers.
  • Organize and coordinate project activities.

Conoscenze

Project management
Communication skills
Analytical skills
Problem-solving skills
Intercultural awareness

Formazione

University degree in Engineering

Strumenti

MS Office
AutoCAD

Descrizione del lavoro

Join us to apply for the Engineering Project Manager (m / f / d) role at Grünenthal Group.

Our team in Manufacturing & Global Operations prioritizes getting things done and continuous improvement. If you are dynamic and positive, you will fit well here. We are an international team committed to high-quality products, constantly seeking improvements across the entire value chain—from raw materials to logistics delivering medicines to patients. Contribute to Grünenthal’s growth by joining us.

What the Job Looks Like

Each day, you'll face challenges such as:

  • Supporting GMP and non-GMP project execution from a technical and project management perspective within the Project Engineering team.
  • Acting as a key contact for external suppliers and liaising with all project team members on site.
  • Organizing and coordinating project activities with stakeholders, ensuring deadlines are met.
  • Participating as a Project Leader or Team Member throughout all project phases.
  • Developing feasibility studies, basic designs, defining scope, estimating timelines and costs, drafting and revising Technical Specifications and URS, reviewing offers, negotiating, managing orders, maintaining supplier relationships, controlling costs, and overseeing FAT and SAT processes.
  • Building understanding of GMP, EHS norms, and pharmaceutical regulations.

What You'll Bring To The Table

To succeed in this role, you should have:

  • A university degree in Engineering.
  • 3-5 years of experience in similar roles, preferably in pharmaceutical manufacturing.
  • Knowledge of cGMP, ISO standards, and safety regulations.
  • Proficiency in MS Office and AutoCAD.
  • Business-fluent English skills.
  • Strong project management and communication skills, intercultural awareness, proactive attitude, autonomy, result orientation, analytical and problem-solving skills, curiosity, precision, and a passion for continuous improvement.

Additional Information

  • Seniority level: Associate
  • Employment type: Full-time
  • Job functions: Quality Assurance, Purchasing, Manufacturing
  • Industries: Pharmaceutical Manufacturing, Healthcare, Biotechnology Research

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