Digital Scientist, CMC
Location: Boston
Posted on: June 23, 2025
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Job Description:
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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 Description About the role: Join
as a Digital CMC Scientist to support the planning, development and
execution of the In Sillico First Initiative within Takeda’s
Pharmaceutical Sciences organization. This exciting opportunity is
perfect for experienced candidates who are curious, eager to learn,
and open to working in a global setting on a variety of tasks
related to data modeling, data fabric / architecture, and
integrated process development workflows in the pharmaceutical
R&D context. In this role, you will work closely with the
Sustainable CMC and Innovation team as well as capability leads
from all development functional area to help establish process
models, data structures, development workflows, and best practices
in an environment where formalized regulatory guidance is still
evolving. You will play a key role in supporting the implementation
and operationalization of proof-of-concept development workflows,
resulting in a paradigm shift that emphasizes In Silico methods as
the basis of reducing overall development effort. How you will
contribute: Support the build & deployment of industry-leading in
silico predictive models (both statistical & first principle) to
support full integration of platform performance workflows to
advance pipeline programs which fulfill In-Silico initiative
deliverables. Support the collection & analysis of structured &
unstructured product & process data and generate scientific reports
including conclusions & recommendations. Undertake scientific
research, complex troubleshooting & problem-solving activities
applying Machine/Deep Learning. Be recognized as a technical
resource & expert in PSST for mathematical modeling, harnessing
next generation capabilities in the field of Data Science and
utilization of his/ her technical expertise to contribute across
multiple projects and drive technical & scientific strategy. Keep
abreast of technological advances specific to Digital Acceleration,
Data Science, Data Engineering, Computational Process Development,
Systems Biology, and Advanced Process Control. Support projects,
primarily within a framework of the In-Sillico First initiative via
the following: Review, interpret & communicate data
cross-functionally across PharmSci and project teams. Perform
Statistical/Machine/Deep Learning and other advanced data
techniques for the purpose of deriving better insights from
available datasets. Understand and use different Supervised and
Unsupervised learning techniques, their biases, how and when to
apply them and which methods are the best for a particular
analysis. Be proficient at wrangle raw data sets into a format that
can have advanced methods applied against the resulting data.
Responsible for collaborating with PharSci functions to encourage
technical alignment & successful achievement of shared goals.
Leverages technical skills as a resource/expert across PharmSci.
Contribute to project work which may include multiple projects
within functional area. Plan and implement resolutions to technical
problems/issues, recommends and implements technologies and
innovations. Responsible for authoring relevant sections of
regulatory documents, report and peer-reviewed manuscripts.
Collaborate with vendors and build relationships to gain access to
technologies as needed to deliver on pipeline goals. Act as a
technical expert for emerging digital capabilities Minimum
Requirements/Qualifications: Education and Experience: Bachelors
degree in Data Science, Statistics, Bio-Informatics, Mathematics,
Chemometrics, Chemistry, Biology, Engineering or related
pharmaceutical science and 8 years relevant industry experience, or
Masters degree in Data Science, Statistics, Bio-Informatics,
Mathematics, Chemometrics, Chemistry, Biology, Engineering or
related pharmaceutical science 6 years relevant industry
experience, or PhD in Data Science, Statistics, Bio-Informatics,
Mathematics, Chemometrics, Chemistry, Biology, Engineering or
related pharmaceutical science and 0 years relevant industry
experience Technical Skills Experience in the use of mathematical,
both statistical and first principle, models as well as advanced
process control systems Solid knowledge of the pharmaceutical
industry and its R&D Comfortable working in the according Data
Science environment: using frameworks (e.g. Python, MATLAB, R,
JMP), considering industrial Data Engineering protocols (e.g. OPC,
Modbus) and repositories (e.g. SQL, Oracle, AWS) Ability to analyze
a wide variety of information and data to make management decisions
regarding potential risks associated with product quality and
regulatory compliance. Sound knowledge of current GxP Proven
scientific track record through presentations at scientific
conferences and publication of peer-reviewed manuscripts Some
experience in Project Management Communication & Leadership Skills:
Experience in working in a multi-disciplinary team environment
Demonstratable critical and out-of-the-box thinking ability
Understanding of the structure, functions, and methods of the
global Takeda organization and overall Takeda R&D operations.
Excellent organizational and communication skills. Develops and
maintains relationships with colleagues within manufacturing and
research networks to identify & support potential value-creating
opportunities. Demonstrates ability to negotiate difficult issues
and arrive at mutually beneficial solutions Robust communication
skills are necessary for explaining complex concepts and policies
across all organizational levels and to external stakeholders. This
also includes the ability to mentor teams on knowledge and data
governance standards and practices. Regulatory Knowledge:
Understanding of cGMP requirements, and some experience with
pharmaceutical regulatory documents Familiarity with recent
regulatory guidance on the use of models for new drug production
applications Knowledge of current and upcoming regulatory
requirements around data modeling, data integrity, including
comprehensive understanding of ALCOA principles Leadership
Behaviors: Candidates must demonstrate Takeda's core leadership
behaviors—integrity, accountability, collaboration, and innovation.
This includes maintaining ethical standards, taking proactive
responsibility for data outcomes, effectively collaborating across
diverse teams, and continually seeking innovative approaches to
enhance data governance. Problem-Solving Skills: Strong analytical
and problem-solving skills are essential for identifying and
addressing issues, developing effective solutions, and implementing
changes that enhance data integrity and operational efficiency.
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 offers stimulating
careers, encourages innovation, and strives for excellence in
everything we do. We foster an inclusive, collaborative workplace,
in which our teams are united by an unwavering commitment to
deliver Better Health and a Brighter Future to people around the
world. This position is currently classified as "hybrid" following
Takeda's Hybrid and Remote Work policy. 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: Boston, MA U.S.
Base Salary Range: $111,800.00 - $175,670.00 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 Boston, MA Worker Type
Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes
It is unlawful in Massachusetts to require or administer a lie
detector test as a condition of employment or continued employment.
An employer who violates this law shall be subject to criminal
penalties and civil liability.
Keywords: , Salem , Digital Scientist, CMC, Science, Research & Development , Boston, Massachusetts