Job Description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description How you will contribute: Lead and develop a global team of managers and scientists and their teams in the field of analytical controls and compliance Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all project-related analytical control topics, development requirements and program milestones including global reporting Oversee and manage core tasks for Analytical controls for clinical trial material efforts across four main areas: a) GMP review and control for analytical documents; b) Release testing oversight, Stability and Shelf life; c) Reference Standard Management; d) GMP Quality Systems Contribute to product development from Research to Commercialization by collaborating with multiple functions within the Pharmaceutical Science organization to improve analytical, process and product knowledge. Including the support of transfer of development assets from Research, main ownership starting at start of GMP activities until hand-over to the commercial organization. Contribute to overall functional direction globally and represent function within CMC/Pharmaceutical Science and across the global Takeda organization. Implement and execute externalization activities with external partners, facilitate development of execution plans for each, and ensure completion of agreed upon activities Accountabilities: Responsibility for people and group management Inspire confidence in team members and lead the organization culture, promoting a healthy and inclusive working environment Build future leadership while mentoring direct reports and junior employees Lead and implementation of wider cross-functional/cross divisional strategy and decisions and drives initiatives to completion. Develops and manages strategies for regional and global departmental infrastructure, resources, projects, etc. in conjunction with senior staff and global line and function heads Lead global CMC and Quality key initiatives and represent Pharm Sci to other cross functional stakeholder key initiatives Analyze and synthesize concepts from diverse information –and articulate Develop and set vision and direction of departmental activities and infrastructure with specific focus but not limited to compliance, quality, systems and processes for AD and PS In collaboration with commercial functions, develop and implement strategies to control quality of drug substances and products based on the current Good/Laboratory/Manufacturing Practice (cGMP, cGLP) regulations Harmonization and standardization of AD but also PS processes, reporting, systems and documents in collaboration with Quality. Establishes and manages operational processes within the department/function. Benchmarks current trends within industry for all areas within Analytical Controls also including strategic development and planning of system architecture in alignment and collaboration with partners and stakeholders e.g. GMS/GQ for company wide systems, IT and PSST for new solutions. Look for external benchmarks that help to aid superior performance of products, processes and people Manages complete line function responsibility for all departmental programs and initiatives Demonstrates project oversight and leadership and cross-functional awareness to advance the line function regionally and globally Directs, informs and applies outsourcing strategy for department in conjunction with senior staff and global line and function heads Minimum Requirements/Qualifications: Bachelor degree with 20+ years of experience Advanced degree with 15+ years relevant industry experience Minimum of 10 years of experience working in CMC analytical development area for active pharmaceutical ingredients and drug products under cGMP’s Demonstrates effective project management skills GMP and compliance experience required Analytical method development experience required Regulatory submission experience required with basic knowledge for regulatory guidelines Global cultural awareness, manage inclusively Familiarity with working in a global setting Excellent command of English (all sites). People managerial experience preferred Team player with flexible personality but able to be persistent and assertive Highly reliable, self-motivated, responsible and curious personality open to learn and develop and a pronounced desire for improvement Takeda is proud in its commitment of creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Discover more at takedajobs.com No Phone Calls or Recruiters Please. #LI-KD1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Cambridge, MAU.S. Base Salary Range: The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/or long-termincentives. U.S.based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S.based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Cambridge, MAVienna, AustriaWorker Type EmployeeWorker Sub-Type RegularTime Type Full timeJob Exempt Yes--s-p-m1-- By applying, you consent to your information being transmitted by Monster to the Employer, as data controller, through the Employer’s data processor SonicJobs. See Takeda Pharmaceutical Terms of Use at and Privacy Policy at and SonicJobs Privacy Policy at and Terms of Use at

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