Job Title: Senior Manager, Supplier Quality (Contract Manufacturing)Job Description The Senior Manager, Supplier Quality (Contract Manufacturing) will focus on managing the external manufacturing Supplier Quality Engineering (SQE) team. This role involves leading an engineering team that collaborates with suppliers, product development, procurement, and quality teams to ensure materials meet compliance standards. The position requires oversight of a diverse portfolio of Contract Manufacturing Organization (CMO) and distributed product suppliers, implementation of quality improvement strategies, and alignment with global supplier management requirements. Responsibilities + Demonstrate broad management experience recognized both within and outside the company, showcasing fully developed leadership skills and a deep understanding of critical issues. + Manage and provide leadership for the functional group's development, direction, and effectiveness, adhering to organizational policies and supporting overall business and corporate objectives. + Participate in short and long-term planning processes to establish technical objectives for business unit projects or functional engineering groups. + Utilize technical and managerial expertise to evaluate proposed solutions, adaptations, and modifications to globally used projects and products. + Identify opportunities and initiate prioritization and implementation. + Complete regular resourcing and budgeting for the team, accountable for long-range planning. + Implement and understand FDA or global regulatory requirements as necessary, in collaboration with cross-functional colleagues. + Ensure compliance with company Quality System regulations and safe working practices. Essential Skills + Minimum 10 years of experience, with at least five years in a supervisory capacity. + Experience with program and project management methods, budgeting, and resource planning. + Ability to lead engineering teams, bringing deep domain expertise to diverse projects. + Capability to manage geographically diverse teams and collaborate effectively with CMOs and/or contract design firms. + Advanced understanding of Design Controls and Quality Management Systems for product development and lifecycle management. Additional Skills & Qualifications + Ability to balance commercial and development needs to achieve global business area goals. + Broad management experience recognized as an expert in multiple unrelated functions. + Collaborative work with business segment, regional, and functional product development leaders to establish long-term goals. + Broad theoretical knowledge of management, quality, global regulatory standards, and manufacturing. + Working knowledge of the business's products and therapeutic uses. + Effective leadership, managerial, strategic planning, and global skills. + Exceptional expertise in planning, budgeting, associate development, and project management. + Understanding of technology and methods applicable to the area, including CAD design and packages, FEA packages, industrial design, and rapid prototyping. + Knowledge and effective use of relevant PC software applications. + Demonstrated ability to communicate effectively both verbally and in writing. Work Environment The work environment involves collaboration with diverse teams across various geographical locations, focusing on contract manufacturing in the medical device sector. The position requires working with advanced technology, including CAD design, FEA packages, and industrial design principles. It is essential to maintain compliance with global quality and regulatory standards, ensuring adherence to safe working practices and quality systems. Pay and Benefits The pay range for this position is $160000.00 - $200000.00/yr. Requisition ID: 34079 At Terumo Blood and Cell Technologies, our 7,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. For Terumo, for Everyone, Everywhere. We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient’s life every second of every day and are committed to continuing to increase the number of patients we serve. Advancing healthcare with heart. With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow and be part of a team that is focused on making a difference. Join us and help shape wherever we go next. You create your future and ours. Senior Manager, Supplier Quality (Contract Manufacturing) will focus on the management of the external manufacturing SQE team with function including the daily management, maintenance, and monitoring of the relevant activities of all team members. This involves leading an engineering team that works collaboratively with suppliers, product development, procurement, and quality to ensure compliant materials. Responsibilities include oversight of extensive portfolio of Contract Manufacturing Organization (CMO) and distributed product suppliers, implementation of quality improvement strategies, and alignment of global supplier management requirements. Works collaboratively developing objectives, plans, and global strategies to ensure effective achievement of business goals and objectives. ESSENTIAL DUTIES Demonstrates broad management experience across and recognized as an expert within and outside of the Company with fully developed leadership skills and a deep understanding of a broad issues vital to the company working with multiple functions that are unrelated.Manages and provides leadership for the functional group’s development, direction, and effectiveness, adhering to organizational policies and processes and supporting overall business and corporate objectives.Participates in the short and long term planning process that establishes technical objectives for a business unit project or functional engineering group.Utilizes technical, managerial expertise and creativity to evaluate proposed solutions, adaptations, and modifications to projects and products used globally.Identifies opportunities and initiates prioritization in addition to implementation.Completes regular resourcing and budgeting pertaining to a team. Accountable for long range planning.Implements and understands FDA or global regulatory requirements as necessary, in partnership with cross-functional colleagues.Ensures compliance with company Quality System regulations and safe working practices. MINIMUM QUALIFICATION REQUIREMENTSEducation Bachelor’s degree or equivalent of education and experience sufficient to successfully perform the essential functions of the job may be considered.Bachelor of Science degree or may have a Master of Science degree, in Engineering, preferred. Experience Minimum 10 years’ experience, five (5) of which have been in a supervisory capacity.Requires experience with program and project management methods, budgeting, and resource planning. Skills Demonstrated ability to lead an engineering bringing deep domain expertise to diverse projects.Ability to manage geographically-diverse teams and collaborators, as well as work effectively and efficiently with CMOs and / or contract design firms.Skilled ability to balance commercial and development needs to accomplish global business area goals.Advanced understanding and application of Design Controls and Quality Management Systems to product development and lifecycle management.Broad management experience across and recognized as an expert within and outside of the Company with fully developed leadership skills and a deep understanding of a broad issues vital to the company working with multiple functions that are unrelated.Work collaboratively with business segment, regional and functional product development leaders to establish and nurture long term goals for the team, department, and function.Broad theoretical knowledge of management, quality, global regulatory standards, and or manufacturing.Requires working knowledge of the business's products and therapeutic uses.Effective leadership, managerial, and strategic planning and global skills.Exceptional demonstrated expertise in planning, budgeting, associate development, and project management directed toward achievement of annual, long term, and strategic business plans and goals.Requires an exceptional understanding of technology and methods applicable to the area and the ability to determine appropriate application. Examples may include Workplace Type This is a hybrid position in Lakewood,CO. Application Deadline This position is anticipated to close on Aug 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. 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