Pharmaceutical Design Manager (m/f/d)

Exyte

Agrate Brianza

In loco

EUR 55.000 - 62.000

Tempo pieno

2 giorni fa
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Descrizione del lavoro

Exyte in Milan seeks an experienced Design Manager for our Pharmaceutical Facilities project. You will coordinate disciplines, manage documents and ensure timely execution in a GMP-regulated environment.

The role requires 10+ years in pharma or life sciences, a mechanical/chemical engineering background, fluency in Italian and English, and willingness to travel as part of an international team. Salary €54,500–€61,500 gross annually.

Competenze

  • Bachelor's or Master's degree in Mechanical, Process, Chemical, Energy Engineering or related discipline
  • Minimum of 10 years of experience as Project Engineer, Lead Engineer or Design Manager in pharma/biotech/life sciences
  • Fluent Italian and English
  • Willingness to travel and work in international teams

Mansioni

  • Coordinate disciplines and forecast engineering deliverables against schedule and project milestones
  • Work with procurement, subcontracting, construction and project controls teams
  • Prepare and review material and construction requisitions for mechanical, piping and utilities
  • Manage the preparation of key multidisciplinary project documents (P&IDs, equipment lists, line lists, utility data, design specs)
  • Organize and document multidisciplinary coordination meetings to ensure timely project execution
  • Ensure compliance with GMP requirements and pharmaceutical industry regulations
  • Support design reviews, risk assessments and technical evaluations
  • Report directly to the Project Manager

Conoscenze

Project coordination
GMP familiarity
Multidisciplinary teamwork
English proficiency

Formazione

Bachelor's/Master's in Mechanical/Chemical Engineering

Descrizione del lavoro

Discover your exciting role

We are seeking an experienced Design Manager (m/f/d) for our exciting Pharmaceutical Facilities project in Milan.

Explore your tasks and responsibilities
  • Coordinate disciplines and project activities, control and forecast engineering deliverables against schedule and project milestones
  • Work in close coordination with procurement, subcontracting, construction and project controls teams
  • Prepare and review material and construction requisitions for mechanical, piping and utility systems
  • Manage the preparation of key multidisciplinary project documents (P&IDs, equipment lists, line lists, utility consumption data, design specifications, etc.)
  • Organize, contribute to and document multidisciplinary coordination meetings to ensure timely project execution
  • Ensure compliance with pharmaceutical industry requirements, quality standards and applicable regulations
  • Support design reviews, risk assessments and technical evaluations throughout the project lifecycle
  • Report directly to the Project Manager
Show your expertise
  • Bachelor's or Master's degree in Mechanical Engineering, Process Engineering, Chemical Engineering, Energy Engineering or a related discipline
  • Minimum of 10 years of experience as Project Engineer, Lead Engineer or Design Manager within the pharmaceutical, biotechnology, life sciences or related industries
  • Strong understanding of GMP-regulated environments and pharmaceutical facility design is highly desirable
  • Nice-to-have: Experience working on construction sites and brownfield projects
  • Very good knowledge of Italian and English
  • Willingness to travel and work within multidisciplinary and international teams

The salary range for this position is between € 54,500 and € 61,500 gross per year (full-time). The exact salary will be determined within this range based on objective and transparent criteria, including role scope, qualifications, and relevant professional experience.

Contact:

For further questions and information, please do not hesitate to contact Ilayda Öztürk via E-Mail at ilayda.oeztuerk@exyte.net.

Please note that we only consider applications submitted through our application portal. Applications sent via email will not be considered due to data protection regulations.

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