Job Description
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## **Job Description**
Synthetic Molecule Process Development (SMPD) is responsible for the
development of robust, sustainable, and cost-effective processes for the
manufacture of new synthetic molecule pharmaceuticals, along with methods for
achieving and controlling high standards of purity and quality.
The successful candidate will be recognized as a technical resourceexpert
within SMPD and across Pharmaceutical Sciences and utilize their technical
expertise to contribute across multiple projects, drive technicalscientific
strategy and mentor junior engineers. The Associate Engineering Fellow will be
leading complex programs and will be responsible for all aspects of reaction &
particle engineering, including the development of scale down models for the
study of unit operations, process safety evaluation as well as technical
transfer to external contract manufacturing organizations. He or she will be
collaborating closely with the Chemistry and Technology groups to apply
enabling & emerging development and manufacturing technologies and will be
responsible for helping shape the department’s technology roadmap, based on
pipeline needs and current trends in research.
The ideal candidate will have deep experience in using process analytical
technologies (PAT) in combination with mathematical models (both statistical &
first principle) to enhance process understanding to effectively develop
optimize scale-up and troubleshoot processes. The Associate Engineering
Fellow will have experience with building scale-down equipment and developing
innovative advanced process control strategies for both batch and continuous
processes. The ideal candidate will strive to continuously improve how
pipeline projects are supported and will be developing new workflows to
facilitate and accelerate process development, optimization and understanding
as well as technical transfer to manufacturing, leveraging digital tools,
automation, robotics andor cobotics. He or she will represent Takeda with
universitiesindustrial consortia and drive the group’s publication strategy.
- *How you will contribute:**
- Develops project and or significant technical strategy and leverages technical skill(s) as a resourceexpert within the department.
- Collaborates closely with cross-functional teams, including process chemistry, analytical development, drug product development, manufacturing, quality assurance, and regulatory affairs, to develop and implement effective process engineering strategies.
- Drives process optimization initiatives to improve sustainability, process efficiency, yield, quality, and cost-effectiveness, utilizing expertise in process chemistry and fundamental engineering principles.
- Oversees process scale-up activities from laboratory to pilot plant and commercial-scale production, ensuring smooth technology transfer and process validation.
- Has full accountability for all engineering aspects for complex pipeline projects.
- Initiates complex projects with extraordinary technical challenges and applies strong technical risk assessment skills.
- Owns a disciplinetechnical skill in its entirety and continues to develop expertise in other key technical skills.
- Conducts analysis of technical and conceptual risk through robust process characterization, failure mode analysis, and risk assessment methodologies, identifies trends and defines and champions process or scientific strategies.
- Benchmarks current trends in R&D; and manufacturing technologies.
- Incorporates novel manufacturing, technologies, and industry trends as a key aspect of scientific strategy development.
- Leads small working groups as appropriate to address knowledge gaps in programs linking departmental strategy to strategies of other relevant functions.
- Identifies topics for initiatives and leads localglobal initiatives on behalf of senior staff.
- Recognized as a technical leaderresource by the group and fosters development of technology skill sets within department and among junior staff.
- Acts as a mentor to junior staff.
- Leads the development of novel solutions for complex cross-functional data analysis, modeling, and engineering challenges.
- Contributes to departmental strategy around scientific improvement and new capabilities.
- Coordinates and leads technology transfer to internal or external manufacturing sites or vendors.
- Communicates with senior management of other functions on implementation of infrastructure, technology, work processes, or business processes.
- Responsible for authoring relevant sections of regulatory documents, validation plans, development reports, process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs;), process descriptions and peer reviewed manuscripts.
- Defines outsourcing strategy for department in conjunction with senior staff.
- Proactively identifies vendors and builds relationships to gain access to technologies as needed to deliver against pipeline goals.
- Attends pertinent workshops and conferences. Belongs to a national professional society, actively participates in local and national activities. Presents scientific posters or podia internally and externally to Takeda. Authors internal reports of publication quality and co-authors publishable manuscripts. Represents Takeda in relationships with universities and industrial consortia. Is an inventor on invention disclosures and patents. Authors publications. Contributes to and drives publication strategy within department. Establishes recognition as scientific leader within Takeda.
- *Minimum RequirementsQualifications:**
- A Ph.D. degree with 7+ years of pharmaceutical industry experience; an MS degree with 13+ years of pharmaceutical industry experience; or a BS degree with 15+ years of pharmaceutical industry experience. Degrees in chemical engineering required
- Extensive experience in the use of mathematical, both statistical and first principle, models as well as advanced process control systems preferred.
- Extensive experience in building reaction kinetic models as well as process models preferred.
- Extensive experience in building laboratory and pilot plant equipment preferred.
- Experience in crystallization process development and scale-up with an emphasis on polymorph, purity and particle size control a plus.
- Experience in the use and scale-up of milling technologies (both dry and wet) for particle size control preferred.
- Experience in the use of process analytical technologies (FT-IR, NIR, FBRM, UV-vis, etc.) required.
- Experience in building chemometric models preferred.
- Experience in developing continuous processes a plus.
- Sound knowledge of current Good Manufacturing Practices (cGMP).
- Experience working in a pilot plant a plus.
- Previous experience with the use of contract facilities and managing technical transfers.
- Experience in working in a multi-disciplinary team environment.
- Significant technical and strategic leadership and accomplishments
- Previous experience contributing to regulatory filings, preferably experience with late-stage filings.
- Proven scientific track record through presentations at scientific conferences and publication of peer reviewed manuscripts.
- *Knowledge and Skills:**
- Able to troubleshoot critical issues or problems and determine the causes and possible solutions
- Ability to work well on global cross-functional team.
- Ability to expresses oneself clearly and concisely within team; documents issues andor concerns concisely and comprehensively; adjusts communication style as appropriate for the audience timely and effectively communicates with senior management; technical writing skills to support authorship of internalexternal and approval of internal technical documents
- Excellent time management and prioritization skills to balance several project and departmental objectives
- Recognized specialist in defined scientific area or areas
- Ability 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 use
- Demonstrated involvement in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events and communicating new scientific trends. Interacts with external vendors for projects
- Develops and uses knowledge and interpersonal skills to appropriately influence and guide others towards the accomplishment of departmentfunction goals and objectives
- *More about us:**
At Takeda, we are transforming patient care through the development of novel
specialty pharmaceuticals and best in class patient support programs. Takeda
is a patient-focused company that will inspire and empower you to grow through
life-changing work.
Certified as a Global Top Employer, Takeda offer
Job Tags
Full time, Contract work, Local area,