Process Improvement and Project Management Specialist

Posted 6 Days Ago
Be an Early Applicant
Via Arese, Milano, ITA
In-Office
32K-32K Annually
Entry level
Biotech • Pharmaceutical
The Role
Supports cross-functional project coordination and process improvement within GM&RA by organizing project information, maintaining documentation, tracking timelines and deliverables, preparing reports and dashboards, and following up on action items. The role assists with continuous improvement initiatives, digital tool adoption, risk monitoring, and collaboration across departments. It is designed for a university graduate with no required professional experience, working under senior guidance in an international pharmaceutical environment.
Summary Generated by Built In

Bracco is an international Group active in the healthcare sector and a leader in diagnostic imaging. The Group’s main products are contrast agents sold in over 100 countries, both directly and indirectly through branches, joint ventures and license and distribution agreements.


The Process Improvement and Project Management Specialist supports the Process Improvement and Project Management function within GM&RA by contributing to project coordination, process monitoring, reporting activities and continuous improvement initiatives. The position is intended for a junior profile at the beginning of their professional career after university graduation, working under the guidance of more senior colleagues and the Head of Management Office. The role supports the collection, organization and analysis of project information, the preparation of reports and dashboards, and the follow-up of timelines, milestones, action plans and deliverables across GM&RA Units and Departments. The position also contributes to initiatives aimed at improving operational efficiency, supporting the introduction of digital tools and facilitating collaboration and information exchange across functions.

Key Responsabilities

  • Supports the coordination of cross-functional projects across GM&RA by helping to collect and organize information related to objectives, timelines, milestones, deliverables, resource needs, risks and action items, under the guidance of senior colleagues.

  • Contributes to the preparation and maintenance of project documentation, meeting materials, action logs, status reports and follow-up trackers for GM&RA initiatives, clinical studies and Regulatory Programs.

  • Assists in monitoring project timelines, milestones and deliverables, highlighting delays, inconsistencies or missing information to the relevant project leads or senior team members.

  • Supports ad hoc, cross-functional and continuous improvement initiatives by helping to coordinate inputs from GM&RA Departments and relevant corporate functions.

Education & Professional Experience

  • University degree in Engineering, Science/Pharmacy, Business Administration, Management or related disciplines.

  • No prior professional experience is required; internship, thesis project or academic exposure to project management, process improvement, data analysis or pharmaceutical/healthcare topics would be preferable.

  • Basic understanding of project management principles, timelines, milestones, deliverables and action tracking.

  • Strong organizational skills, attention to detail and willingness to learn in a cross-functional and international environment.

  • Ability to work collaboratively with different functions, collect inputs, follow up on open points and escalate issues appropriately.

  • Basic knowledge of reporting tools and willingness to develop capabilities in project management, risk management and process improvement methodologies.

  • Good analytical mindset and ability to organize information, prepare summaries and support data-driven monitoring activities.

  • Knowledge of clinical study or regulatory processes would be a plus.

  • Proficiency in Microsoft Office tools, in particular Excel and PowerPoint; knowledge of Power BI would be a plus.

  • Basic financial awareness and willingness to understand internal accounting and cost control processes.

  • Good written and spoken English.

Employment terms:

The role is classified at Level D under the National Collective Agreement for the Chemical-Pharmaceutical Industry (CCNL Chimico-Farmaceutico).
The guaranteed minimum base annual gross salary established by the CCNL for the applicable level is € 31.990,56
The overall compensation will be determined based on the experience, skills, and qualifications of the selected candidate.


Contract type:

Fixed Term

If you meet the requirements of this opportunity and would like to join an international group working to improve patients' lives, apply now!

At Bracco, we believe in the values of diversity and inclusion. We respect and celebrate the diversity of our people and their experiences, ensuring a fair opportunity for all.

We are #Bracco #JoinUs

Skills Required

  • University degree in Engineering, Science, Pharmacy, Business Administration, Management, or a related discipline
  • No prior professional experience required
  • Basic understanding of project management principles, timelines, milestones, deliverables, and action tracking
  • Strong organizational skills and attention to detail
  • Willingness to learn in a cross-functional and international environment
  • Ability to collaborate with different functions, collect inputs, follow up on open points, and escalate issues appropriately
  • Basic knowledge of reporting tools and willingness to develop project management, risk management, and process improvement capabilities
  • Good analytical mindset and ability to organize information, prepare summaries, and support data-driven monitoring
  • Knowledge of clinical study or regulatory processes
  • Proficiency in Microsoft Office, particularly Excel and PowerPoint
  • Knowledge of Power BI
  • Basic financial awareness and willingness to understand internal accounting and cost control processes
  • Good written and spoken English
  • Internship, thesis project, or academic exposure to project management, process improvement, data analysis, or pharmaceutical and healthcare topics
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The Company
HQ: Milan
1,975 Employees

What We Do

Bracco is an international Group active in the healthcare sector and a leader in diagnostic imaging. It has around 3,700 employees and annual total consolidated revenues of around 1,7 billion euros, 89% of which from international sales. In the R&D area, the company invests approximately 10% of reference turnover in the imaging diagnostics and medical devices sectors. The Group’s main products are contrast agents, medical substances used to improve the diagnostic accuracy of biomedical imaging and the care of patients affected by diseases of varying type and severity. Bracco offers an extensive and innovative portfolio of products and solutions for all diagnostic modalities completed by several medical devices and advanced administration systems for contrast imaging products in the fields of cardiology and radiology, developed by it’s American company ACIST. Since its foundation, Bracco has been a socially responsible company in each area of activity - in business as in every other context. Its subsidiary Bracco Imaging is one of the world’s leading companies in the diagnostic imaging field :X-Ray Imaging (including Computed Tomography-CT), Magnetic Resonance Imaging (MRI), Contrast Enhanced Ultrasound, and Nuclear Medicine. The Company operates in over 110 markets: in North America through Bracco Diagnostics Inc. USA , and with an affiliate in Montreal (Canada); in Europe, with offices in all major countries; in Japan (BRACCO-EISAI). The Company also operates in South America, South Korea and China through its 70% controlled Joint Venture, Bracco Sine Pharmaceutical Corp. Ltd.

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