Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. The Director of Business Development – Cell Therapy will drive business growth strategies with a specialized focus on human biological raw materials, cell sourcing, and regulatory compliance in cell therapy processes. This role requires a strategic leader with deep scientific knowledge and the ability to oversee cross-functional project implementation to ensure successful execution. As the company’s SME, the candidate will provide insight into process development, infrastructure needs, and resource planning, guiding Bio Supplies in building capabilities necessary for success in cell therapy. *This is a remote opportunity* **Responsibilities include but are not limited to:** _Business Development Strategy_ 1. Lead the development of a business strategy for cell therapy, emphasizing human biological raw materials, cell sourcing, and therapeutic applications. 2. Identify and pursue new market opportunities to expand our influence and revenue in the cell therapy space. 3. Conduct thorough market analysis to keep our strategy aligned with industry trends and competitive dynamics. _Subject Matter Expertise (SME) and Capability Building_ 1. Serve as the Bio Supplies' SME on human biological raw materials, advising on required processes, resources, and best practices in cell therapy. 2. Assess current capabilities and provide recommendations on infrastructure needs, such as facility construction or resource allocation, to support business goals. 3. Guide internal stakeholders on critical areas of development, including cell sourcing standards, lab capabilities, and other operational requirements. _Project Management Oversight_ 1. Oversee the project management aspects of business development initiatives, ensuring alignment with strategic objectives and efficient execution. 2. Provide guidance on setting milestones, tracking progress, and making adjustments to meet business goals, rather than managing individual projects. 3. Support teams in translating strategic goals into actionable plans that align with regulatory and market demands. _Regulatory and Compliance Leadership_ 1. Ensure compliance with FDA, EMA, and other relevant regulatory guidelines related to human biological raw materials in cell therapy. 2. Lead the development of policies and processes to navigate regulatory challenges in the cell therapy space. 3. Keep teams informed of regulatory updates and best practices to maintain compliance. _Strategic Partnerships and Client Relations_ 1. Build and maintain strategic partnerships with suppliers, clients, and industry stakeholders. 2. Represent the company as a trusted resource and primary contact for clients in the cell therapy industry, along with the sales team. 3. Work with sales and marketing teams to effectively communicate our value proposition. Every employee, regardless of their professional group, has the following activities inherent to their position: - Knowledge and application of work standards (GMP, PNT, INS, BPL, etc...) according to defined procedures. - Compliance with records, if any. - Monitoring of established quality, safety, hygiene and environmental standards. - Inform the direct manager of any incident in the normal development of their work. - Carry out the tasks of the lower professional groups, if necessary. This Job Description is intended to present the general content and requirements for the performance of this position. The description should not be construed as an exhaustive statement of duties, responsibilities or requirements. Managers and supervisors may assign other responsibilities as needed. **Skills/Qualifications/Education:** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. + Bachelor degree in Life Sciences, Cell Biology, Biochemistry required + Bachelor degree required and 10 years of related experience or Master with 8 years + 8-10 years of business development experience in cell therapy or related biotechnology fields, with a focus on human biological raw materials and cell sourcing + Proven expertise in assessing and advising on infrastructure and resource needs in cell therapy, including lab capabilities and other technical requirements + Strong regulatory knowledge, with an understanding of FDA, EMA, and other relevant guidelines in cell therapy + Demonstrated ability to build strategic plans and execute them to achieve measurable business outcomes + Excellent communication and interpersonal skills, with the ability to influence stakeholders and foster partnerships + Knowledge and application of work standards (GMP, PNT, INS, BPL, etc...) according to defined procedures + Compliance with records, if any + Monitoring of established quality, safety, hygiene and environmental standards + Inform the direct manager of any incident in the normal development of their work + Carry out the tasks of lower professional groups, if necessary *Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate’s degree with 6 years of experience, or a Master’s degree with 2 years of experience It will comply with and enforce the policy on occupational risk prevention and the objectives established in SST. It is responsible for ensuring the appropriate conditions of the jobs in its area of ​​action through compliance with the prevention measures adopted in each case, including health surveillance. It will take into account any suggestions for improvement that are proposed. They will promote and participate in the development of safe work procedures, guaranteeing their compliance, and will participate in the preventive activities assigned to them based on the job and position they occupy. They will use and ensure the appropriate use in accordance with their nature and the foreseeable risks of the machines, devices, tools, dangerous substances, transport equipment, personal protective equipment and, in general, any other means with which they carry out their activity. It will ensure the adequate training and information of its collaborators about the risks existing in the workplace and the preventive and protective measures to be adopted. You will work to integrate health and safety into jobs within the organization. Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 4-6 hours per day. Frequent hand movement of one hand with the ability to make fast, simple, movements of the fingers, hands, and wrists. Frequently walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to site locations and travels within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Frequently interacts with others, relates sensitive information to diverse groups. Ability to apply abstract principles to solve complex conceptual issues. Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Plans work assignments to meet objectives **Pay Scale:** The estimated pay scale for the Director Business Development, Cell Therapy role based in the United States (non-California), is $170,000.00-$220,000.00 per year. Additionally, the position is eligible to participate in the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, 9 paid Holidays per year, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us! **For California:** The estimated pay scale for the Director Business Development, Cell Therapy role based in San Francisco, San Carlos or Emeryville, California, is $190,000.00- $250,000.00 per year. The estimated pay scale for the Director Business Development, Cell Therapy role based in all other cities in California is $180,000.00 - $240,000.00 per year. \#LI-CB1 Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. **Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws.** Learn more about Grifols (https://www.grifols.com/en/what-we-do) **Req ID:** 521404 **Type:** Regular Full-Time **Job Category:** Others