Principal Scientist, Analytical Chemistry in Late Stage Biopharma (Hiring Immediately)

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’s Privacy 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 DescriptionJoin Takeda as a Sr. Scientist, Analytical Development (AD), Late Stage Development where you will independently lead efforts in development of analytical methods, implementation of evolving scientific technology and influences strategic planning within AD and across Pharmaceutical Sciences to deliver on program strategy and initiatives. You will also prepare and coordinate completion of technology transfer documentation, CMC sections of regulatory documents, or validation plans and reports within expertise for review. You will drive analytical strategy as needed by the business and support in-silico and automation initiatives. As part of the Analytical Development team, you will report to Director, Analytical Development.How you will contribute : Develop and leverage analytical strategic understanding of project and CMC priorities to plan / coordinate with cross-functional peers and evaluate impact of decisions across CMC functions and other development functions.Contribute to complex / multiple projects or functional areas through leading or influencing others.Influence and support initiatives related to driving scientific and technical improvement both within the analytical function and cross-functionally.Review, interpret, and communicate data cross functionally within CMC and project teams.Coordinate with others in creating technical reports including reviewing and editing.Conduct analysis of technical and conceptual risk and trends.Identify process trends and define process strategy or use of novel technologies.Recognized as a technical expert and resource within function. Expertise in dissolution is preferred.Technical responsibility for a project area / technical program within the department and potentially across CMC.Represent functional area on CMC project teams by communicating activities from designated functional area to project team.Integrate scientific / technical efforts around cross-functional issues.Lead local / global initiativesEnsure a productive and development-rich environment; Serve as a technical resource or mentor for junior staff and leverage expertise in laboratory technology as a functional resource / trainer.Define more complex / novel approaches and methodologies to solving complex technical challenges.Identify vendors and build relationships to gain access to technologies as needed to deliver pipeline goals.Manage key vendor relationships across projects as appropriate and affect resolution of issues arising at vendors.Initiate and influences project direction outside department.Prepare and review technical reports and regulatory filing documentation.Coordinate cross-functional teams and resolutions, with a focus on scientific / technical challenges.Minimum Requirements / Qualifications : Bachelors degree in chemistry, biology, pharmacy, or related pharmaceutical science and 11 years (Sr. Scientist) or 8 years (Scientist) relevant industry experienceMasters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 9 years (Sr. Scientist) or 6 years (Scientist) relevant industry experiencePhD in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 3 years (Sr. Scientist) relevant industry experienceExtensive experience in CMC pharmaceutical development for active pharmaceutical ingredients and drug products under cGMP'sExperience with late-stage synthetic molecule analytics is required. Additional experience with liposomes, LNPs, peptides and oligonucleotides would be advantageous.Extensive experience in dissolution method development and strategy, including regulatory interactions, is essential.Experience with in-silico and automation technology approaches to support program execution.Have developed expertise in multiple areas of analytical technology and demonstrate an in-depth working knowledge of program strategy.Knowledge of analytical techniques with advanced experience in multiple techniques for synthetic molecules such as LC, GC, dissolution, KF, particle size analysis, etc.; Able to work in a lab setting and independently interpret results of complex experiments and integrate data produced by other disciplinesIn-depth experience with analytical method strategy for dissolution including method development, validation and statistical and modeling approaches preferred.Experience with method development, validation (phase appropriate and ICH), and transfer; Ability to design and direct analytical strategy to meet CMC project objectivesAble to coordinate resources (internal / external) to support a projectAble to expresses oneself clearly and concisely within team; documents issues and / or concerns concisely with colleagues; adjusts communication style as appropriate for the audience; timely and effectively communicates with senior management; has sound technical writing skills to support authorship and approval of internal technical documents.Subject matter expertise in a specific scientific area or areas. Demonstrated ability to successfully contribute across multiple scientific endeavorsAbility to capture knowledge within the organization; improves solutions, processes, and deliverables through use of information; improves information capital by contributing experience, theories, deliverables, and models for others to useDemonstrated involvement in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events preferredLeadership Skills- Develops and uses knowledge and interpersonal skills to appropriately influence and guide others towards the accomplishment of department / function goals and objectivesExperience representing Analytical Development in a cross functional CMC environmentSound knowledge of current Good Manufacturing Practices (cGMP)Experience with the use of contract facilitiesExperience contributing to regulatory filingsExperience working in a multi-disciplinary team environmentTakeda Compensation and Benefits SummaryWe 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 : Boston, MAU.S. Base Salary Range : $133,000.00 - $209,000.00The 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-term incentives. 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-

Salary : $133,000 - $209,000