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Strategic Project Manager - SHS Radiopharma EU (f/m/d)

Vacature ID
482855
Geplaatst sinds
27-okt-2025
Vakgebied
Engineering
Ervaringsniveau
Mid-level Professional
Type functie
Fulltime
Werkwijze
Alleen op kantoor/werkplaats
Type contract
Vast contract
Locatie(s)
  • Esplugues de Llobregat - Barcelona - Spain
  • Saint-Genis-Pouilly - Auvergne-Rhône-Alpes - France

At Siemens Healthineers (SHS) Radiopharma, we are committed to driving sustainable progress through cutting-edge technology. We empower our customers by bridging the physical and digital worlds—enhancing the way we live, work, and move, today and for future generations. 

We believe that business success begins with our people. That’s why we prioritize a culture where individuals thrive. Our diverse team is ready to support, inspire, and challenge you to grow in new and meaningful ways. Together, there are limitless possibilities of where our shared journey may lead.


We are looking for a Strategic Project Manager. This position will be preferably based in either Barcelona (Spain) or Saint-Genis-Pouilly (France)


As the global leader in the supply of positron emission tomography (PET) radiopharmaceuticals, SHS Radiopharma pioneered the commercial PET radiopharmacy model over 30 years ago—and continues to shape the future of molecular imaging.

We are seeking an experienced and driven quality professional to join SHS Radiopharma as a Strategic Project Manager, a critical leadership role supporting the expansion of our European operations. In this role, you will lead the expansion of manufacturing capacities at existing facilities, drive the creation of new facilities to support production of our current PET diagnostic portfolio, and develop new manufacturing capacities for our growing pipeline of radiopharmaceutical theranostic products, spanning both clinical development and commercial phases.

With a global network of 58 cyclotron-equipped facilities, Radiopharma offers the opportunity to reimagine your career with an industry innovator dedicated to delivering precision theranostics and improving patient outcomes worldwide.


Join us and help shape the future of precision theranostics while advancing patient care.

 

Your responsibilities in this role will be focused, but not limited to :

  • Initiating projects within your area of expertise, defining key attributes such as scope, cost, schedule, quality, risks, communications, stakeholders, resources, procurement, and change management. 
  • Collaborating with internal and external stakeholders to ensure proper project definition, alignment, and compliance with required procedures.
  • Establishing mechanisms to effectively lead, manage, monitor, and control projects during their execution phase.
  • Leading and managing project teams throughout the full project lifecycle.
  • Ensuring efficient handover of project outcomes to operational teams at project close (first patient dose).
  • Contributing to building the new Project Management Department, fostering synergies and harmonizing procedures. 
  • Supporting local teams in managing and applying project management standards and internal procedures to local initiatives.

 

The role will require the following skills :


Technical Project Management: Proven ability to manage multiple complex projects efficiently; project management training required. (Minimum 3 years)

Strategic & Business Management:

  • Experience in a management role within cGMP manufacturing facilities. (Minimum 3 years)
  • Expertise in manufacturing radiopharmaceuticals for various applications, including PET products (F-18, Ga-68) for diagnostics and long-lived isotopes (Lu-177, Ac-225, etc.) for therapy. (Minimum 5 years) 

Leadership:

  • Demonstrated experience managing multidisciplinary teams. (Minimum 3 years)
  • Proven track record engaging with management and leadership boards. (Minimum 3 years)
  • Strong collaboration with multidisciplinary departments across multinational organizations. (Minimum 3 years)

You’ll win us over by having the following qualifications:


Abilities:

  • Ability to work independently and interpret complex financial and technical information.
  • Strong technical skills with proven ability to troubleshoot, solve abstract issues, and implement policies and procedures. 
  • Skilled in communicating and promoting a common vision while fostering a high-performance team culture.
  • Demonstrated leadership abilities with effective personnel and cross-functional management.
  •  Proven ability to manage and engage a large, decentralized team.
  • Capacity to assess strategic impact of initiatives and resolve highly complex, cross-functional challenges.
  • Strong interpersonal, organizational, and managerial skills.
  • Excellent attention to detail and accuracy in execution of responsibilities.
  • Ability to successfully manage multiple tasks in a fast-paced environment.

 

Education [Minimum/Preferred]:

  • B.S. or M.S. degree in Engineering, Chemistry, Pharmacy, or related sciences (minimum).
  • Master’s degree in Project Management (strongly preferred).

Languages:

  • Proficient in English, both written and spoken.

 

Experience:

  • Minimum 5 years of experience in the development and/or manufacture of radiopharmaceuticals under cGMP.
  • Minimum 3 years of experience in managing projects.
  • Strong interpersonal, organizational, and managerial skills.


Job Dimensions:

  • Direct Reports: 0
  • Geographic Scope: United Kingdom, EMEA & APAC Region
  • Impact on Organization: High – this role is pivotal to the success of SHS Radiopharma’s expansion strategy by driving the timely delivery of new manufacturing capacities, ensuring projects are executed within scope, budget, and regulatory expectations, and enabling the introduction of new diagnostic and therapeutic products to market. Effective leadership in this role ensures alignment of cross-functional teams, seamless technology transfer, and operational readiness to meet patient and customer needs. A lack of leadership or delays in execution could result in significant financial loss (e.g., missed revenue from delayed product launches), reputational damage, operational inefficiencies, and potential regulatory setbacks that could impact patient access to critical therapies.
  • Reporting Lines: Program Coordinator (UK, EMEA & APAC)

 

Travel: Required to perform job function (up to 50%)