Blueprint Medicines is a biopharmaceutical company dedicated to revolutionizing the treatment of patients with genomically defined cancers, rare diseases, and cancer immunotherapy. Through innovative science and precision medicine, Blueprint Medicines is committed to developing highly selective therapies that target the underlying genetic drivers of disease to deliver meaningful outcomes for patients.

Regional Marketing Executive, Northeast

Scientist I, Biology

Associate Architect, Infrastructure and Operations

Manager, Compensation

Medical Science Liaison, NYC

Medical Director, Allergy/Immunology, Pulmonology, or Dermatology

Medical Science Liaison, New England, Hematology/Allergy

Therapy Area Lead, Allergy & Immunology

Field Access Expertise Leader

Co-op, Medicinal Chemistry Address: 45 Sidney Street Cambridge, MA, 02139 Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. Responsibilities: We are seeking a highly motivated and enthusiastic co-op intern to join our medicinal chemistry team. This lab-based internship will provide an introductory experience into the drug discovery process. Working under the supervision of a senior chemist, the intern will design and synthesize novel chemical matter for evaluation in a preclinical program. The intern will analyze and interpret data to build upon existing structure activity relationships, informing the design of subsequent generations of targets. In addition to developing their skills in multistep organic synthesis, the intern will learn and apply basic principles of medicinal chemistry, including structure-based drug design, ADME properties, and PK optimization. Projects will be crafted along one or multiple of the following key areas based on interest and business needs:&nbsp; Propose potential synthetic routes and carry out multistep organic synthesis to generate novel chemical matter. The chemist will utilize a variety of chemical reactions, purification techniques (extraction, crystallization, silica chromatography, reverse-phase HPLC, etc.), and analytical techniques (LC-MS, NMR, etc.), and practice good record-keeping in an electronic notebook.&nbsp;&nbsp; Present data and summarized results both orally and in written form, within multidisciplinary team meeting&nbsp;&nbsp; Take detailed notes about the experimental design and conditions, record these experimental results in both electronic notebook and presentation format&nbsp; Learn and practice the basic principles of structure-based drug design (SBDD) through data analysis and practice designing new compounds, using software such as D360, LiveDesign, Flare, Spark, and Maestro.&nbsp; Meet weekly with their manager to discuss progress and review relevant topics in organic and medicinal chemistry (tailored to the intern’s level of chemistry education).&nbsp;&nbsp; Attend weekly chemistry team meetings and provide a monthly update to the chemistry team.&nbsp; Perform other duties as assigned. ONSITE EXPECTATIONS (DAYS PER WEEK): This is a lab-based position, we expect 5 days on site.&nbsp; Qualifications: Senior, or Master’s/PhD level, pursuing a degree in Chemistry or a related major&nbsp; Must have successfully completed Organic Chemistry courses (I and II or equivalent) with lab.&nbsp; What additional qualifications will make you a stronger candidate? Interested in organic synthesis, medicinal chemistry, chemical biology, and drug discovery.&nbsp; Experience in multi-step organic syntheses preferred. Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism Our Co-op Program: Blueprint’s Co-op program is ~6 months long. The program is designed to provide students with deep functional expertise within their department and a broad understanding of the life sciences industry. Co-ops are paired with dedicated mentors for personalized learning and career development guidance. The program includes lunch and learn sessions, networking events, a student volunteer day, and other networking opportunities. It culminates in a final poster presentation where interns showcase their work. Dress Code: Blueprint’s offices are a business casual environment. Business casual means attire that is professional but also relaxed, such as slacks or business dress pants, skirts/dresses, khakis, chinos, or dark jeans without holes paired with button-down shirts, sweaters, blouses, or polo shirts and closed-toed shoes. It typically excludes formal suits or very casual clothing such as athletic wear or flip flops. Spring 2026 Co-op Program Dates: Monday, January 5th – Friday, June 26th &nbsp;&nbsp; Pay Range: Our Co-ops are paid hourly based on previous Co-op experience. The expected pay range for this role is $27.00 - $32.00 per hour. Who will my employer be? You will be employed by Magnit, LLC for all purposes and not Blueprint Medicines, a Sanofi Company. As your employer, Magnit will assign you to provide services to Blueprint as a co-op or intern. Under this arrangement, co-ops and interns will have the opportunity to learn about Blueprint Medicines, a Sanofi Company and gain meaningful hands-on experience. Please note: Co-op and interns are not employees of Blueprint in any way, and do not qualify for participation in Blueprint’s benefit plans.&nbsp; Equity, Diversity, Inclusion and Affirmative Action “To do our best work we need different viewpoints. Therefore, we celebrate diversity and embrace inclusion.&nbsp; As an equal opportunity employer, we are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills.&nbsp; We strive to ensure that we maintain a positive and enriching work environment for all.”&nbsp; For more information on Magnit’s privacy notice, click on privacy notice. Magnit, LLC recognizes the importance of individually held beliefs re: appropriate dress/attire and will reasonably accommodate an employee’s religious beliefs unless the accommodation creates an undue hardship. Those requesting attire accommodation based on religious beliefs should reach out to their Magnit representative. Magnit is a Global industry leader with one simple goal of shaping and delivering the next chapter in workforce management for our employees, clients, suppliers, and partners around the world.&nbsp; Why Blueprint? At Blueprint Medicines, a Sanofi Company, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.

Co-op, Medicinal Chemistry

Co-op, Biology Drug Discovery &nbsp; Address: 45 Sidney Street Cambridge, MA, 02139 &nbsp; Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. &nbsp; Responsibilities: We are seeking a motivated graduate-level co-op student interested in contributing to our drug discovery programs, with a focus target validation and assay development for testing candidate drug compounds. This student will apply advanced molecular biology techniques to evaluate candidate compounds and contribute to the scientific direction of our programs. Projects will be crafted along one or multiple of the following key areas based on interest and business needs: Lab Work: Design, execute, and analyze in vitro cellular assays across a variety of cell lines to assess drug efficacy and biological impact Perform mechanism of action studies on human and engineered cell lines, including proliferation assays, signaling assays, protein-protein interactions, and high content imaging assays Maintain cell cultures, generate stable cell lines using RNA interference (RNAi) or gene editing techniques (CRISPR/Cas-9) Execute drug combination studies on cell lines of interest to evaluate synergistic or antagonistic effects. Data Analysis and Documentation: Analyze experimental data using GraphPad Prism, Excel, and other relevant tools Maintain accurate and detailed electronic laboratory notebooks in compliance with Blueprint Medicines’ standards Collaboration and Communication: Participate in regular team meetings, present findings, and contribute to scientific discussions Collaborate with cross-functional teams, seek feedback, and actively contribute to a culture of innovation Perform other duties as assigned. &nbsp; ONSITE EXPECTATIONS: This is a lab-based position, and the Co-op is expected to work onsite 5 days/week. &nbsp; Qualifications: Currently enrolled student pursuing a PhD or master's program in biomedical sciences, molecular biology, or related field 1-2 years of independent laboratory research Strong foundation in cellular and molecular biology Proficiency in core lab techniques (e.g., tissue culture, Western blotting, DNA/RNA extraction, immunofluorescence, cell proliferation and viability assays, experience generating cell lines a plus) &nbsp; What additional qualifications will make you a stronger candidate? Strong commitment to pursuing a career in research Excellent communication, organizational, and analytical skills Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Our Co-op Program: Blueprint’s Co-op program is ~6 months long. The program is designed to provide students with deep functional expertise within their department and a broad understanding of the life sciences industry. Co-ops are paired with dedicated mentors for personalized learning and career development guidance. The program includes lunch and learn sessions, networking events, a student volunteer day, and other networking opportunities. It culminates in a final poster presentation where interns showcase their work. &nbsp; Dress Code: Blueprint’s offices are a business casual environment. Business casual means attire that is professional but also relaxed, such as slacks or business dress pants, skirts/dresses, khakis, chinos, or dark jeans without holes paired with button-down shirts, sweaters, blouses, or polo shirts and closed-toed shoes. It typically excludes formal suits or very casual clothing such as athletic wear or flip flops. &nbsp; Spring 2026 Co-op Program Dates: Monday, January 5th – Friday, June 26th&nbsp; &nbsp; &nbsp; Pay Range: Our Co-ops are paid hourly based on previous Co-op experience. The expected pay range for this role is $32.00 - $35.00per hour. &nbsp; Who will my employer be? You will be employed by Magnit, LLC for all purposes and not Blueprint Medicines, a Sanofi Company. As your employer, Magnit will assign you to provide services to Blueprint as a co-op or intern. Under this arrangement, co-ops and interns will have the opportunity to learn about Blueprint Medicines, a Sanofi Company and gain meaningful hands-on experience. Please note: Co-op and interns are not employees of Blueprint in any way, and do not qualify for participation in Blueprint’s benefit plans.&nbsp; &nbsp; Equity, Diversity, Inclusion and Affirmative Action “To do our best work we need different viewpoints. Therefore, we celebrate diversity and embrace inclusion.&nbsp; As an equal opportunity employer, we are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills.&nbsp; We strive to ensure that we maintain a positive and enriching work environment for all.”&nbsp; For more information on Magnit’s privacy notice, click on privacy notice. Magnit, LLC recognizes the importance of individually held beliefs re: appropriate dress/attire and will reasonably accommodate an employee’s religious beliefs unless the accommodation creates an undue hardship. Those requesting attire accommodation based on religious beliefs should reach out to their Magnit representative. Magnit is a Global industry leader with one simple goal of shaping and delivering the next chapter in workforce management for our employees, clients, suppliers, and partners around the world. &nbsp; Why Blueprint? At Blueprint Medicines, a Sanofi Company, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.

Co-op, Biology Drug Discovery

How will your role help us transform hope into reality? Research, identify, and validate novel oncology targets and small molecule drug discovery, utilizing knowledge of bioengineering to develop and conduct cellular assays to support Blueprint Medicine’s novel drug discovery efforts.&nbsp; &nbsp; What will you do? Manages and QC routines assays performed at CRO and upload data to our server. (15%) Optimize and employ cellular and molecular assays such as Western blotting, Elisa and immunofluorescence-based assays to elucidate mechanistic biology of potential drug targets and mechanism of action of small molecules. (20%) Present research findings at team meetings. (5%) Maintain our automation platform and is the point of contact with the vendor when needed (such as major issues to be fixed or implementation of new updates). (15%) Design and development of automation methods for biological assays for several projects. Teach colleagues how to use those methods and troubleshoot when necessary. (15%) Cell culture Maintenance. (10%) Run routine assays when needed. (10%) Maintain detailed and critical experimental data records that are published in ELN according to industry compliance. (10%) &nbsp; What minimum qualifications do we require? Master’s degree in Bioengineering, Biomedical Engineering, or a closely related biological or life sciences field (or foreign equivalent degree), plus 1 year of experience in biological research for oncology drug development.&nbsp; Experience, which may be gained concurrently, must include: 1 year of experience in maintaining, expanding, and freezing cell lines. 1 year of experience with running routine assays such as Alphalisa pERK and proliferation assays. 1 year of experience in using and programming liquid handlers such as Bravo, Biomek, Integra Assist Plus and D300. 1 year of experience in analyzing cell research data and presenting it to the team. 1 year of experience in analyzing and presenting scientific research papers. 1 year of experience in maintaining detailed ELN to ensure data reproducibility. * This position is part of Blueprint Medicines’ employee referral program and is eligible for an employee referral incentive bonus. &nbsp; Why Blueprint? At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Equal Employment Opportunity At Blueprint Medicines, we foster an environment of fair treatment and full participation for all of our employees as we navigate complex challenges in pursuing our mission to improve the lives of patients. We celebrate our unique differences and varied career and life experiences so that we can sustain our diverse culture and ensure everyone feels accepted. We are committed to non-discrimination, equal employment opportunity, as well as an inclusive recruitment process. We consider all qualified applicants based on merit and without regard to race, color, sex, gender identity, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable federal or state law. &nbsp; &nbsp;We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of an accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com. We are also an E-Verify Employer. For more information, please see our EEO Policy Statement, the E-Verify Participation Poster, the Right to Work Poster, and the EEO Know Your Rights Poster.&nbsp; &nbsp; Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the&nbsp;U.S.&nbsp;and&nbsp;Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit&nbsp;www.BlueprintMedicines.com&nbsp;and follow us on&nbsp;X&nbsp;(formerly Twitter; @BlueprintMeds) and&nbsp;LinkedIn. Requisition #: 25-604&nbsp; #LI-DNI &nbsp;

Associate Scientist Biology

Location(s): Zug, Switzerland Level of position: Associate Director Position type: 60% field-based, 40% home-office based Reporting Line: This role reports to the Director of International Medical Affairs &nbsp; How will your role help us transform hope into reality? The Field Medical Advisor role at Blueprint Medicines Alpine is a critical position within the organization, responsible for providing medical, scientific and strategic expertise to support Switzerland’s and Austria’s development and commercialization programs. As a Field Medical Advisor, you will play a key role in driving the success of Blueprint's mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research, market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas, new innovations, and new ways of thinking to help advancing a diverse portfolio of innovative therapies for mast cell disorders, including systemic mastocytosis and chronic urticaria, and cancer. &nbsp; What will you do? With deep knowledge of the country's KOLs landscape, proactively manages KOL pool in the interest of Blueprint at the country level Establish and maintain strong relationships with, and be recognized by KOLs, HCPs and PI’s as Blueprint reference point and connector. Drives engagement of HCPs, professional societies and other key customers, including patients advocacy groups. Fosters the establishment and maintenance of local scientific advisory boards, round tables, expert meetings and scientific advocacy development. Develops and maintains scientific and medical and scientific knowledge and maintains an awareness of relevant industry and market trends (i.e., competitive, technological, social and economic). Participates in gathering clinical insights, needs and feedback from medical specialists and other stakeholders in the market, acts upon them and communicates to/shares with internal partners Remains informed of current developments within pertinent medical and scientific communities through familiarity with current literature, attendance at meetings, conventions, professional associations, etc. Works closely with local, regional and global market access colleagues in preparing strong price and reimbursement dossiers that will be tested extensively with medical experts and national leaders. May also have to represent it to reimbursement authorities.&nbsp; Alignment with the Global and EU/International team on plans and processes. Drives the local Medical Plan development and its execution Actively supports upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities. Reviews and signs off local educational and promotional material as the responsible information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development, Clinical Operations, and Global Medical Affairs teams. Ensures a strategic approach to such programs, and the development of clinical data to support the appropriate use of the Company's products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/o for access needs. Collaborates closely with market access for HEOR, access required information &nbsp; What minimum qualifications do we require? Advanced Clinical/Scientific degree (PhD, MD, PharmD, MSc) is required&nbsp; Minimum 3 years in Pharmaceutical industry, preferably Medical Affairs positions (MSL, Medical Advisor/Manager) is required.&nbsp; Prior experience in working in Biotech or Biopharm industries is an advantage. Excellent written and oral communication skills in the languages of the region, including strong formal presentation skills in those languages. &nbsp; What additional qualifications will make you a stronger candidate?&nbsp; Proficient on Entrepreneurial Spirit &amp; Action Highly Proficient on Ownership &amp; Execution Highly Proficient in Authentic Relationship Building Proficient in Strategic Prioritization Proficient as Impact Multiplier Demonstrable experience in the implementation of launches (pre and post-launch plans).&nbsp; Solid understanding of the capabilities of the medical affairs function in general, the Hematology/Oncology/Allergology &nbsp;medical environment &nbsp;as well as Regulatory, HTA, Early Access Program and RCTs requirements. Ability to maintain scientific credibility through effective scientific communication Superior ability and leadership presence to represent Blueprint Medicines in the medical community as an ambassador. Has confidence and optimism, enabling the development of strong relationships internally and externally with executive level leaders. Demonstrates respect for others by seeking to understand how they think about issues/opportunities; has an appreciation for others’ strengths/development areas to increase overall collaboration and performance, is able to listen attentively. Seeks input from team to make key decisions while ensuring final decisions are reached quickly and effectively. Has strong business acumen and courage of one’s convictions; however, stands by organizational decisions once made. Ability to create and implement strategic plans in a “green field” environment, can prioritize and execute independently, is a self-starter and has a ‘sleeves rolled up’ approach. Entrepreneurial and innovative of spirit. High degree of emotional intelligence, displaying candor and integrity at all times, combined with the ability to manage complexity, ambiguity and paradoxes during the build out of the region. Understanding of pharmaceutical commercial, access, medical and scientific needs on a local basis. Experience with product launches. Solid knowledge of country level regulations, guidelines, codes of practices and Access requirements Operational excellence: management skills, planning, prioritization, decision making, objective setting and plan execution. Strong customer orientation; science-based, but good understanding of marketing needs; negotiation skills. Solid peer relationships with exposure to scientific and clinical experts, with a demonstrated ability to engage internal and external leaders. Experience delivering effective and persuasive communications on complex and controversial matters to both corporate management and scientific audiences. Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors. *Blueflex is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer. &nbsp;

Field Medical Advisor, Alpine

Location(s): Vienna, Austria Level of position: Associate Director Position type: 60% field-based, 40% home-office based; Temporary&nbsp; Reporting Line: This role reports to the Director of International Medical Affairs &nbsp; How will your role help us transform hope into reality? The Field Medical Advisor role at Blueprint Medicines Alpine is a critical position within the organization, responsible for providing medical, scientific and strategic expertise to support Switzerland’s and Austria’s development and commercialization programs. As a Field Medical Advisor, you will play a key role in driving the success of Blueprint's mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research, market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Field Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas, new innovations, and new ways of thinking to help advancing a diverse portfolio of innovative therapies for mast cell disorders, including systemic mastocytosis and chronic urticaria, and cancer. &nbsp; What will you do? With deep knowledge of the country's KOLs landscape, proactively manages KOL pool in the interest of Blueprint at the country level Establish and maintain strong relationships with, and be recognized by KOLs, HCPs and PI’s as Blueprint reference point and connector. Drives engagement of HCPs, professional societies and other key customers, including patients advocacy groups. Fosters the establishment and maintenance of local scientific advisory boards, round tables, expert meetings and scientific advocacy development. Develops and maintains scientific and medical and scientific knowledge and maintains an awareness of relevant industry and market trends (i.e., competitive, technological, social and economic). Participates in gathering clinical insights, needs and feedback from medical specialists and other stakeholders in the market, acts upon them and communicates to/shares with internal partners Remains informed of current developments within pertinent medical and scientific communities through familiarity with current literature, attendance at meetings, conventions, professional associations, etc. Works closely with local, regional and global market access colleagues in preparing strong price and reimbursement dossiers that will be tested extensively with medical experts and national leaders. May also have to represent it to reimbursement authorities.&nbsp; Alignment with the Global and EU/International team on plans and processes. Drives the local Medical Plan development and its execution Actively supports upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities. Reviews and signs off local educational and promotional material as the responsible information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Supports interventional and non-Interventional clinical trials in close collaboration with with Clinical development, Clinical Operations, and Global Medical Affairs teams. Ensures a strategic approach to such programs, and the development of clinical data to support the appropriate use of the Company's products. Works with colleagues of Blueprint Medicines International headquarter in Zug and other countries in the international region to ensure consistency of clinical programs from a medical perspective. Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/o for access needs. Collaborates closely with market access for HEOR, access required information &nbsp; What minimum qualifications do we require? Advanced Clinical/Scientific degree (PhD, MD, PharmD, MSc) is required&nbsp; Minimum 3 years in Pharmaceutical industry, preferably Medical Affairs positions (MSL, Medical Advisor/Manager) is required.&nbsp; Prior experience in working in Biotech or Biopharm industries is an advantage. Excellent written and oral communication skills in the languages of the region, including strong formal presentation skills in those languages. &nbsp; What additional qualifications will make you a stronger candidate?&nbsp; Proficient on Entrepreneurial Spirit &amp; Action Highly Proficient on Ownership &amp; Execution Highly Proficient in Authentic Relationship Building Proficient in Strategic Prioritization Proficient as Impact Multiplier Demonstrable experience in the implementation of launches (pre and post-launch plans).&nbsp; Solid understanding of the capabilities of the medical affairs function in general, the Hematology/Oncology/Allergology &nbsp;medical environment &nbsp;as well as Regulatory, HTA, Early Access Program and RCTs requirements. Ability to maintain scientific credibility through effective scientific communication Superior ability and leadership presence to represent Blueprint Medicines in the medical community as an ambassador. Has confidence and optimism, enabling the development of strong relationships internally and externally with executive level leaders. Demonstrates respect for others by seeking to understand how they think about issues/opportunities; has an appreciation for others’ strengths/development areas to increase overall collaboration and performance, is able to listen attentively. Seeks input from team to make key decisions while ensuring final decisions are reached quickly and effectively. Has strong business acumen and courage of one’s convictions; however, stands by organizational decisions once made. Ability to create and implement strategic plans in a “green field” environment, can prioritize and execute independently, is a self-starter and has a ‘sleeves rolled up’ approach. Entrepreneurial and innovative of spirit. High degree of emotional intelligence, displaying candor and integrity at all times, combined with the ability to manage complexity, ambiguity and paradoxes during the build out of the region. Understanding of pharmaceutical commercial, access, medical and scientific needs on a local basis. Experience with product launches. Solid knowledge of country level regulations, guidelines, codes of practices and Access requirements Operational excellence: management skills, planning, prioritization, decision making, objective setting and plan execution. Strong customer orientation; science-based, but good understanding of marketing needs; negotiation skills. Solid peer relationships with exposure to scientific and clinical experts, with a demonstrated ability to engage internal and external leaders. Experience delivering effective and persuasive communications on complex and controversial matters to both corporate management and scientific audiences. Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors. *Blueflex is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer. &nbsp;

Field Medical Advisor, Alpine (Temporary)

Location:&nbsp;Denmark, Sweden, Norway, Finland Level of position: Senior Manager Position type: Field-based, Temporary (1 year contract) Reporting Line: Senior Director, P&amp;MA Lead DACH, Nordic Countries &nbsp; How will your role help us transform hope into reality? As Key Account Manager Nordics you will contribute to a successful launch with AYVAKYT in Denmark, Sweden, Norway and Finland, build a new market to help patients with systemic mastocytosis, and focus on market development within their territories. You will be a product and disease state expert responsible for building sustainable relationships with assigned HCPs in the territory. You will be the 1st manager in the region to build up a network and contribute to access for SM patients to this new treatment, working with cross functional colleagues to deliver best in class patient support. You will report to the Nordics Countries Lead. &nbsp; What will you do? Apply strong clinical acumen to effectively educate on relevant products and disease states to target HCP’s; hematologists, oncologists, allergists, immunologists, as well as the broader care team in academic and community practice settings Apply strong business acumen to effectively build relationships and manage accounts by engaging a variety of healthcare stakeholders including account leadership, mid-level providers, nursing, pharmacy, and patient access support functions Engage accounts on patient pull-though strategies including dispensing support, patient access engagement, and patient management strategies to ensure appropriate utilization Exhibit a patient focused mindset while delivering educational resources and programs to assist with effective patient care Build and maintain relationships with key accounts and customers, involving cross-functional stakeholders as needed to manage key relationships of national and/or regional relevance Builds collaborative partnerships and operates effectively in a matrix environment; expert collaboration with cross-functional partners, including marketing, training, operations, advocacy, medical, etc. Build relationships and maintain effective communication with internal stakeholders Develop effective business plans aimed at achieving set objectives Proactively identify new opportunities and apply customer insights to develop, execute and refine approaches Leverage analytical tools to understand business trends and meet or exceed target KPIs; Represent Blueprint Medicines at congresses and local / regional medical meetings Ability to travel within the Nordic countries on a regular basis, which may include overnight and weekend travel Comply with regulatory guidelines, public policies/guidelines, and corporate policies and procedures &nbsp; What minimum qualifications do we require? BA/BS degree required or bachelor’s degree 5+ years’ experience in biotech/ pharma sales calling on relevant specialists 5+ years experience in Allergy/Immunology, Hematology, and/or Rare Disease Resides within the territory &nbsp; What additional qualifications will make you a stronger candidate? Degree preferably in Health Sciences, Business, Marketing, Accounting, or related field&nbsp; Consistent success in driving above-plan sales results within a specific region/territory Strong clinical background in applicable specialties is required; hematology, oncology, allergy/ immunology. Rare disease experience is preferred. Understanding of disease modifying therapies with a requisite diagnostic component and ability to navigate patient pull through in complex market access environments Proven ability to develop and expand new markets. Exceptional interpersonal and communication skills to form strong, trusting partnerships to drive performance Robust analytical and problem-solving skills, ability to identify and action on creative solutions Ability to establish credibility, connect the dots and align multiple stakeholders to pioneer the adoption of new products, methods and technologies A team player able to collaborate effectively with a broad range of stakeholders, gain consensus and act independently in a fast-paced, entrepreneurial environment Flexibility and the ability to plan and nimbly adapt to changing market conditions Motivated by patient focus, urgency and personal commitment to high performance, results and compliance Possesses high integrity and exceptional work ethic Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism&nbsp; &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.&nbsp; This is the place where the extraordinary becomes reality, and you could be part of it.&nbsp;&nbsp; Patients are waiting. Are you ready to make the leap?&nbsp; &nbsp; &nbsp;Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that seeks to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success, leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit www.BlueprintMedicines.com and follow us on X (formerly Twitter; @BlueprintMeds) and LinkedIn.&nbsp; &nbsp;*Blueflex is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer.&nbsp;

Key Account Manager, Nordics

Location(s): Rome, Italy Level of position: Associate Director Position type:&nbsp;65% Office-based, 35% Field-based (Or office-based with 30% business travel) Reporting Line: The position reports to the Country Medical Lead &nbsp; How will your role help us transform hope into reality? The Medical Advisor role at Blueprint Medicines is a critical position within the organization, responsible for providing medical, scientific and strategic expertise to support Italy’s development and commercialization programs. As a Medical Advisor, you will play a key role in driving the success of Blueprint's mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research, market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas, new innovations, and new ways of thinking to help advancing a diverse portfolio of innovative therapies for mast cell disorders, including systemic mastocytosis and chronic urticaria, and cancer.&nbsp; &nbsp; What will you do? Proactively manage KOLs in the interest of Blueprint at the country level through your deep knowledge of the country's KOLs landscape. Establish and maintain strong relationships with KOLs, HCPs and PI’s and be recognized by them as Blueprint’s reference point and connector. Represent the company at relevant medical conferences and symposia. Foster the establishment and maintenance of local scientific advisory boards, round tables, expert meetings and scientific advocacy development. Closely cooperate with the country Medical Lead supporting the execution of medical plans as well as taking over the co-ordination of specific scientific projects. Cultivate a trustful and effective two-way collaboration with MSLs, supporting their presence in the field. Provide a source of key medical knowledge on the company’s products and ensure that all regulatory requirements are met and aligned with local and Global standards. Maximize your skills in critically analyzing and interpreting clinical trial data, real-world evidence, and scientific literature. You will communicate the clinical implications of data and contribute to the development of scientific publications and presentations. Collaborate in insights collection and analysis to be translated into guidance for internal colleagues from different functions across the company. Leverage your expertise and excellence to contribute to the development and execution of the medical strategy. Build strong collaborative relationships with cross functional team to ensure alignment with medical and business objectives. Actively support upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities. Develop and deliver medical education programs for internal teams, healthcare professionals, and other stakeholders. Collaborate closely with International Medical teams to identify key data/material gaps and help in developing medical material and resources. Review product presentations and training materials, provide medical input into promotional campaigns and provide medical input in the health benefit discussion related to new products. Support interventional and non-Interventional clinical trials in close collaboration with Clinical development, Clinical Operations and Global Medical Affairs teams. Ensure a strategic approach to such programs, and the development of clinical data to support the appropriate use of the Company's products. Actively support the Medical Lead in developing and executing patient advocacy strategies, fostering meaningful partnerships with patient organizations and advocacy groups. Ensure that patient perspectives are integrated into medical plans, scientific communications, and strategic decision-making, in alignment with our patients first value. &nbsp; &nbsp;What minimum qualifications do we require? Advanced Clinical/Science degree or professional credentials required (PhD, MD, PharmD, MSc). 5+ years of experience in the biotech or pharmaceutical industry in a similar role. &nbsp; What additional qualifications will make you a stronger candidate? Excellent communication and presentation skills, with the ability to effectively communicate complex scientific concepts to diverse audiences. Familiarity with established and emerging regulatory frameworks (including AI, GDPR, EFPIA and Farmindustria) to ensure compliance and strategic alignment in medical activities. Demonstrable experience in the implementation of launches (pre- and post- launch plans). Solid understanding of the capabilities of the medical affairs function, the Hematology/Oncology/Allergy medical environment as well as Regulatory, HTA, Early Access Program and RCTs requirements. Seek input from the team to make key decisions while ensuring final decisions are taken quickly and effectively. Solid customer orientation; science-based, but good understanding of marketing needs; negotiation skills. Immunology/allergy and/or oncology/hematology experience preferred. Flexibility, with positive attitude, strong ability to multitask, prioritize projects effectively and communicate at all levels within the company. Ability to critically assess, adopt and integrate digital and innovative tools into medical affairs practice (RWE, PROs, digital biomarkers) Has confidence and optimism, enabling the development of strong relationships internally and externally with executive level leaders. Demonstrate respect for others by seeking to understand how they think about issues/opportunities; has an appreciation for others’ strengths/development areas to increase overall collaboration and performance. Strong business acumen and courage of one’s convicitons; however, stands by organizational decisions once made. High degree of emotional intelligence, always displaying candor and integrity, combined with the ability to manage complexity. Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.&nbsp; This is the place where the extraordinary becomes reality, and you could be part of it.&nbsp;&nbsp; Patients are waiting. Are you ready to make the leap?&nbsp; &nbsp; &nbsp;Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that seeks to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success,&nbsp;leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit www.BlueprintMedicines.com and follow us on X (formerly Twitter; @BlueprintMeds) and LinkedIn.&nbsp; &nbsp; &nbsp;*Blueflex&nbsp;is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer.&nbsp;

Medical Advisor, Italy

Location(s): United Kingdom Territory:&nbsp;Primarily UK with responsibility for the Nordics (20%) Level of position: Level 8&nbsp; (Senior Manager) Position type: Field-Based, based in England with strong transport links and near an airport which can provide travel to other countries within the geographical scope Reporting Line: Reports to the International Medical Director &nbsp; How will your role help us transform hope into reality? At Blueprint Medicines, we are driven by purpose and precision. As a Medical Science Liaison (MSL), you will serve as a trusted scientific expert, facilitating high-quality medical engagement and education on our innovative therapies. You will cultivate strong relationships with healthcare professionals (HCPs) and key opinion leaders (KOLs) to support our mission of delivering transformative therapies to patients with genomically defined diseases. In addition to UK responsibilities, you will strategically support MSL work across the Nordic countries, requiring a strong grasp of cross-border collaboration and cultural fluency. Your ability to navigate a complex healthcare environment and integrate learnings across geographies will be key. &nbsp; What will you do? Be Blueprint Medicines’ scientific ambassador in the UK and Nordics. Short term focus is England, Wales and Denmark. Mid- term focus will be additional countries including Scotland, Republic of Ireland and Sweden. Provide support to Blueprint’s first commercialized asset known as Ayvakyt. This will involve proactive identification, engagement, and maintainenance of scientific exchange with KOLs and healthcare professionals in Systemic Mastocytosis, this includes HCPs across allergology, immunology, hematology, oncology, and rare diseases. Provide accurate, balanced, and timely scientific and clinical support aligned with company strategy across the HCPs within the designated country remit. Gather insights from field interactions to inform internal strategies and plans. Deliver impactful, evidence-based presentations to both external and internal stakeholders. Support local execution of company-sponsored studies and investigator-initiated trials (IITs). Contribute to the planning and execution of regional and international scientific meetings, advisory boards, and symposia. Maintain a robust understanding of disease area landscape and healthcare systems in the UK and Nordics. Collaborate cross-functionally with Medical Affairs, Clinical Development, Regulatory, and Commercial teams. Champion compliance, ethical behavior, and scientific integrity in all activities. Uphold and model Blueprint Medicines’ five core organizational competencies. Willingness to travel extensively within the UK and to the Nordics &nbsp; What minimum qualifications do we require?&nbsp; Advanced Clinical/Scientific degree (PhD, MD, PharmD, MSc) Rare disease or hematology or Oncology launch experience 3+ years’ experience as an MSL or similar field-based medical role in the biopharma industry Candidate must reside within the UK and be in close proximity to a major airport&nbsp; &nbsp; What additional qualifications will make you a stronger candidate?&nbsp; A deep knowledge of allergology/immunology would also be an advantage. Prior experience in working in Biotech or Biopharm industries is an advantage Fluency in English (written and spoken); knowledge of a Nordic language is a plus Strong presentation and communication skills, with the ability to simplify complex scientific data Experience working across multiple countries or regions, particularly in Europe Cultural agility and ability to build relationships in a diverse cross-border setting Demonstrated ability to navigate complexity with clarity and confidence Self-starter attitude with strong organizational and time management skills Ability to demonstrate strong proficiency in the following Blueprint competencies: Entrepreneurial Spirit &amp; Action, Authentic Relationship Building, and Ownership &amp; Execution. They should also be actively developing proficiency in Strategic Prioritization and Impact Multiplier. Entrepreneurial Spirit &amp; Action: You take initiative, remain flexible in dynamic settings, and make bold, responsible decisions to move things forward. Authentic Relationship Building: You foster trust, unify diverse teams, listen deeply, and collaborate effectively across borders and disciplines. Strategic Prioritization: You understand the big picture, identify what matters most, and focus your energy on work with the greatest impact. Ownership &amp; Execution: You demonstrate resilience, deliver results, and continuously reflect and adapt to improve your impact. Impact Multiplier: You elevate others, foster inclusion, seek feedback, and cultivate high performance within and across teams. &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? Blueprint&nbsp;Medicines, a Sanofi company, is a global biopharmaceutical company that seeks to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success,leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit&nbsp;www.BlueprintMedicines.com&nbsp;and follow us on&nbsp;X&nbsp;(formerly Twitter; @BlueprintMeds) and&nbsp;LinkedIn. *Blueflex is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer. &nbsp;

Medical Science Liaison, UK

Location: Boston, MA &nbsp; How will your role help us transform hope into reality? The Precision Medicine Executive (PME), Region will play a meaningful role setting the foundation for commercial success as we deliver through multiple product launches and indication expansions for patients with solid tumors and a rare hematologic disorder. The primary focus will be to improve the diagnosis of systemic mastocytosis to support the commercial success of AYVAKIT. You will be responsible for driving adoption and utilization of quality diagnostic testing in key accounts to identify patients who may be candidates for Blueprint Medicines’ portfolio of precision therapies in oncology and rare diseases, with a focus on systemic mastocytosis . You will report to the Director, Precision Medicine Executive Field Leader, and be a key member of an efficient, effective, and highly collaborative field team regionally aligned with field sales. &nbsp; What will you do? Be responsible for cultivating stakeholder relationships and developing account-specific plans to facilitate use of high quality, biomarker/genomic testing to ensure optimal diagnosis Demonstrate knowledge of, access to, and the ability to build and manage relationships with all key stakeholders in targeted accounts (Pathologist, Executive Leadership, Lab personnel, etc.) Apply strong technical acumen to effectively educate on diagnostic testing and disease state to key stakeholders (including broader care team and treating clinicians) and how it fits in the treatment paradigm in SM. Deliver educational materials and programs, partnering with marketing, sales, and medical affairs appropriately Proactively identify and communicate customer issues, educational opportunities, and market developments with regional partners and broader Precision Medicine team Serve as a diagnostics subject matter expert for the region Develop business plans for each target account aligned to strategic imperatives Represent Blueprint Medicines at congresses and medical meetings, including pathology meetings Form relationships with diagnostic laboratories and identify partnership opportunities Travel within the US on a regular basis, which may include overnight and weekend travel Align with regulatory guidelines, public policies/guidelines, and corporate policies and procedures &nbsp; What minimum qualifications do we require?&nbsp; BA/BS degree OR equivalent work experience required 5+ years experience in biotech, pharma or diagnostic laboratory setting Ability to travel within the US on a regular basis, including overnight and weekend travel Candidate must reside in or near Boston, MA &nbsp; What additional qualifications will make you a stronger candidate? MBA, advanced degree in life sciences, medical or pharmacy degree preferred Strong technical background in pathology, molecular biology and/or diagnostics applicable to hematology, oncology or rare diseases Demonstrated success across multiple drug launches in applicable specialty markets Understanding of diagnostics market considerations including regulatory, reimbursement, and policy, as well as familiarity with patient, provider, and payer perspectives on diagnostic testing Strong oral and written communication skills Robust analytical and problem-solving skills, ability to identify and action on creative solutions Ability to establish credibility, connect the dots and align multiple stakeholders to pioneer the adoption of new products, methods and technologies A teammate able to collaborate effectively with a broad range of partners, influence without authority, gain consensus, and act independently in a fast-paced, entrepreneurial environment Flexibility and the ability to plan and nimbly adapt to changing conditions Motivated by patient focus, urgency and personal dedication to high performance, results and compliance Possesses high integrity and exceptional work ethic Commitment to Blueprint Medicines’ Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Why Blueprint? At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Equity, Diversity, Inclusion and Affirmative Action At Blueprint Medicines, we&nbsp;foster an environment of fair treatment and full participation&nbsp;for&nbsp;all of our employees as we navigate complex challenges in pursuing our mission to improve the lives of patients. We celebrate our unique differences and varied career and life experiences so that we can sustain our diverse culture and ensure everyone feels accepted. We are&nbsp;committed to non-discrimination, equal employment opportunity, as well as an inclusive recruitment process. We consider all qualified applicants based on merit and without regard to race, color, sex, gender identity, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable federal or state law.&nbsp; &nbsp;&nbsp; We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of an accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com. We are also an E-Verify Employer. For more information, please see our&nbsp;EEO&nbsp;Policy Statement, the&nbsp;E-Verify Participation Poster, the&nbsp;Right to Work Poster, and the&nbsp;EEO&nbsp;Know Your Rights Poster. &nbsp; Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the&nbsp;U.S.&nbsp;and&nbsp;Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit&nbsp;www.BlueprintMedicines.com&nbsp;and follow us on&nbsp;X&nbsp;(formerly Twitter; @BlueprintMeds) and&nbsp;LinkedIn. #LI-Remote #LI-AQ1 &nbsp;

Precision Medicine Executive, Northeast

How will your role help us transform hope into reality? The Senior Director, Direct-to-Patient (DTP) Team Lead will be responsible for further establishing and maintaining a leadership position for Blueprint Medicines, a Sanofi Company, among the patient and caregiver community living with systemic mastocytosis (SM). Your strategic vision will ensure we have an wholistic patient and caregiver engagement strategies, including groundbreaking patient marketing strategies and initiatives for SM and AYVAKIT (avapritinib), a potential multi-billion opportunity. Working collaboratively with cross-functional partners, you will represent the Voice of the Patient and be the driving force behind patient engagement strategies that not only speak to patients but also reinforces our Patient First mindset.&nbsp;&nbsp; &nbsp;AYVAKIT’s ongoing launch into Indolent Systemic Mastocytosis (ISM), provides a unique opportunity to continue to build a new market and reach a patient community that had no therapeutic option until now that treated the underlying driver of disease. While ISM is a rare disease, it is extremely underdiagnosed with 9 years average time to diagnosis after seeing several types of medical specialists.&nbsp;&nbsp; You will lead the Patient Marketing team, which is collectively responsible for creating and implementing strategies across disease awareness and product promotion to support personal and non-personal/digital promotion for patient audiences. Reporting to the Vice President, Commercial Strategy &amp; Marketing, you will be a leader in both the marketing team and broader patient connect team across the organization. Working closely with cross-functional partners: Patient Advocacy, PR/Corp Communications, Regional Marketing, Commercial Operations, and US Market Access/Patient Services is crucial to brand success. Your collaborative efforts will ensure a cohesive and patient-centric approach across all patient touchpoints.&nbsp;&nbsp; &nbsp; What will you do? Lead the US AYVAKIT patient marketing team, develop an industry-leading DTP team who are enthusiastic about patient marketing. Your strategic guidance and mentorship will empower them to deliver impactful campaigns and initiatives.&nbsp;&nbsp; Provide leadership to Blueprint Medicines and brand team to enable development, alignment and execution of patient strategy across the organization &nbsp; Spearhead cross-functional collaboration and alignment to ensure patient strategies are integrated across Blueprint Medicines, including leading broader patient connect team across organization &nbsp; Collect actionable patient insights that help understand the SM landscape, identify the emergent needs of SM patients and caregivers, guiding and encouraging understanding of insights cross functionally &nbsp; Guide the development and execution of core patient-facing initiatives, including the disease awareness campaign, AYVAKIT campaign updates, digital/print media, conferences, and non-personal tactics &nbsp; Provide strategic oversight for the Patient Ambassador Program (unbranded and branded), including programming strategy, goals and KPIs &nbsp; Lead digital marketing capability evolution (in collaboration with commercial operations) to ensure team can execute on multichannel promotion campaigns &nbsp; Accountable to patient-focused brand plan, proposing programs and capabilities needed to support the strategy and championing that plan through engagement with cross-functional partners &nbsp; Collaborate with legal, regulatory, and compliance stakeholders to ensure compliant development and execution of educational programming &nbsp; &nbsp; What minimum qualifications do we require? BA/BS degree required; advanced degree, MBA, or other equivalent experience preferred &nbsp; Minimum of 12+ years of experience in strategic roles within the biotech/pharmaceutical industry, including direct involvement in marketing, sales, or market development activities &nbsp; Previous in-line marketing experience a must, with core focus on patient strategy, franchise management, and cross-functional leadership&nbsp; Required travel: Up to 25% &nbsp; &nbsp; What additional qualifications will make you a stronger candidate? Deep experience in developing patient engagement strategies &amp; tactics for pharmaceutical or biotech products in the US &nbsp; Demonstrated ability to work effectively on cross-functional matrix teams, leading without authority &nbsp; Expertise with omnichannel, media planning, and integrated promotion with an emphasis on digital and social media strategy &nbsp; Experience working on launch products where DTP is central to brand success needed &nbsp; Experience in rare disease, oncology and/or new markets preferred &nbsp; Demonstrated track record of complex project management and effective vendor management &nbsp; Excellent written and communication skills &nbsp; Proven ability to influence without authority and work with cross-functional teams in the development and delivery of brand strategic imperatives &nbsp; A team player who can take an enterprise view, influence without authority, gain consensus rapidly and act independently in a fast-paced environment &nbsp; Broad degree of professional versatility with internal drive and curiosity to take on new and challenging roles and responsibilities &nbsp; Flexibility and the ability to plan and nimbly adapt strategy and approaches to changing conditions &nbsp; Motivated by patient focus, urgency and personal commitment to high performance, results and compliance. Possesses high integrity and exceptional work ethic &nbsp; Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; Why Blueprint? At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Equity, Diversity, Inclusion and Affirmative Action At Blueprint Medicines, we&nbsp;foster an environment of fair treatment and full participation&nbsp;for&nbsp;all of our employees as we navigate complex challenges in pursuing our mission to improve the lives of patients. We celebrate our unique differences and varied career and life experiences so that we can sustain our diverse culture and ensure everyone feels accepted. We are&nbsp;committed to non-discrimination, equal employment opportunity, as well as an inclusive recruitment process. We consider all qualified applicants based on merit and without regard to race, color, sex, gender identity, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable federal or state law.&nbsp; &nbsp;&nbsp; We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of an accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com. We are also an E-Verify Employer. For more information, please see our&nbsp;EEO&nbsp;Policy Statement, the&nbsp;E-Verify Participation Poster, the&nbsp;Right to Work Poster, and the&nbsp;EEO&nbsp;Know Your Rights Poster. &nbsp; Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines, including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in the&nbsp;U.S.&nbsp;and&nbsp;Europe. Leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit&nbsp;www.BlueprintMedicines.com&nbsp;and follow us on&nbsp;X&nbsp;(formerly Twitter; @BlueprintMeds) and&nbsp;LinkedIn. #LI-Hybrid #LI-AQ1 &nbsp;

Senior Director, Direct to Patient Team Lead

Location(s): Munich, Germany Level of position: Senior Manager Position type: Office-based, in alignment with BlueFlex model* Reporting Line: Senior Director, P&amp;MA Lead DACH, Nordic Countries &nbsp; How will your role help us transform hope into reality? The Senior Manager Market Access &amp; Corporate Affairs Germany will manage Pricing &amp; Market Access (PMA) for AYVAKYT (avapritinib) in indolent and advanced systemic mastocytosis as well as plan and execute communication &amp; PR and Patient Affairs &amp; Governmental Affairs activities. The purpose is to identify the needs of patients, healthcare providers and payers in Germany and address challenges and opportunities to maximize access, communicate with stakeholders and contribute to BPMs success. Analyze and assess market access insights, develop strategies and solutions for implementation is key with this role. &nbsp; What will you do? Support with HTA (AMNOG) assessment procedure including written statement and oral hearing; Develop materials for payer engagement initiatives; Support price negotiations with pricing analysis, pricing intelligence and HEOR initiatives; Manage regional and local hurdles and opportunities with Avapritinib and support field teams; Develop and execute the PR/communication plan aligned with brand strategy; Analyze and assess Governmental regulations on national and local level with impact for BPM and develop recommendations to strengthen BPM business; Engage with patient organizations and present BPM as partner in systemic mastocytosis. &nbsp; What minimum qualifications do we require? Academic education and experience from similar positions (life science, economics, media) Minimum of 5+ years’ experience in pharmaceutical/biotechnology field Strong knowledge of Market Access and HTA/Payer requirements, standards and processes, including experience with national and regional authorities, including sick funds and other payers Experience with communications and PR initiatives Experience to manage complex projects and colaborate with multi-disciplinary teams Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism &nbsp; What additional qualifications will make you a stronger candidate? &nbsp; Ability to lead PMA initiatives and work as part of a team under uncertainty with a “can do” attitude Ability to prioritize and drive for results with an emphasis on quality. Ability to analyze diverse sets of complex information and distill into recommended strategy Computer skills (MS Office programs) Fluency in German and English, both oral and written Effective communication skills at all levels both internally and externally In-depth understanding of health insurance systems such as reimbursement pathways, HTA&nbsp;and contracting opportunities &nbsp; &nbsp; &nbsp; &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success. This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap? &nbsp; Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors. As of July 17th2025 Blueprint Medicines is a Sanofi company. *Blueflex is our operating model which optimizes culture, productivity, &amp; flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility.&nbsp; Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources.&nbsp; It is a culture enhancer. &nbsp;

Senior Manager, Market Access & Corporate Affairs

&nbsp; Are you looking for an opportunity to stay connected with our company and be the first to hear about exciting career opportunities? Join our Talent Community to stay in the know and pave the way for your potential future with Blueprint Medicines.&nbsp; &nbsp; What We're Looking For: We're interested in individuals who are eager to explore new career opportunities, keep an eye on industry trends, and become part of our talent network. Whether you're actively job hunting or just curious about future prospects, our Talent Community is for you. &nbsp; Why Blueprint?&nbsp; At Blueprint Medicines, we achieve&nbsp;impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.&nbsp; This is the place where the extraordinary becomes reality, and you could be part of it. Patients are waiting. Are you ready to make the leap?&nbsp; &nbsp; Ready to Connect? Join our Talent Community today and unlock a world of possibilities. We look forward to staying connected in the near future! &nbsp; #LI-DNI

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