Job Detail

 In this role you will be supporting the implementation of the Treatment Center network, the coordination of treatment and the patient pathway and the set-up of the bluebird bio business. You will collaborate with bluebird bio cross-functional teams in Europe and USA including Commercial Operations, Quality Assurance, Finance and the Global Pharmaceutical Science Organization to accomplish bluebird bio’s objectives in Europe for product launch, patient treatment and lifecycle management. 

Your role at bluebird bio

• Collaborate with European and Global stakeholders to support set up and onboarding of Treatment Centers


• Support the Treatment Center readiness through Kick Off, Pre-boarding &, Onboarding


• Assist in the expansion of the Treatment Center network


• Coordinate the update and enhancement of Treatment Center engagement materials with global stakeholders


• Collaborate in the setup of Treatment Center training activities


• As needed, support the implementation of the bluebird bio infrastructure in Europe and the individual country models


• Manage Change Control execution for country launches and Treatment Center establishment


• Work closely with the Quality organization to ensure GDP compliance


• Follow up IT developments in terms of enhancement requests, testing and IT deployment


• Continuous improvement: Engage in the identification, sharing, and adaptation of best practices cross functionally and between Treatment Centers


• Facilitate effective working relationships with internal and external customers


• Provide support within the Patient Supply Team

About you: 

• Bachelor's degree or the combination of education and business experience required


• Minimum 3 years relevant experience (e.g. supply chain, corporate training) in healthcare or another regulated environment


• Excellent communication and presentation skills are necessary


• 5-10% travel may be required related to this role


• Good understanding of GxP is required


• Experience supporting cross functional initiatives and building and implementing processes with large groups of stakeholders


• Experience with commercial launches


• Experience with IT projects is ideal but not required


• Experience within a cellular or gene therapy organization is ideal but not required


• Highly self-motivated individual, with demonstrated ability to work independently in an extremely fast-paced and complex environment


• Fluent in English, Italian and/or French and ideally German but not required


• Eligible to work in Switzerland


• Ready and excited to embrace the principles of the bluebird bio culture: b colorful, b cooperative, and b yourself

bluebird bio is committed to fostering an environment where everyone can be their whole selves and know they are valued. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. As an employer, we do not discriminate on the basis of race, religion, color, national origin, age, gender (including pregnancy, childbirth, or related medical conditions), sex, sexual orientation, gender identity, gender expression, age, disability, or other personal characteristics.

To all recruitment partners: bluebird bio does not accept resumes. Please do not forward resumes to our jobs alias, our birds or any other organization location. bluebird bio is not responsible for any fees related to unsolicited resumes.