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Job DescriptionThe Occupational, Environmental and Product Quality Toxicology (OEPQT) team within DSRE provides toxicology risk assessments supporting Takeda’s Environmental Health and Safety (EHS) and pharmaceutical manufacturing functions that will assist with specification setting, manufacturing site selection, appropriate containment and controls, maintaining product quality attributes, and employee and patient safety.
This position is for a remote intern toxicologist in the Drug Safety Research and Evaluation (DSRE) group at Takeda. In this role the candidate will contribute to data collection, storage, and analysis for use in toxicology risk assessments supporting Environmental Health and Safety (EHS), Pharmaceutical Sciences, and manufacturing functions within Takeda. This includes toxicology support for impurity qualifications, extractables and leachables, environmental risk assessments (ERA), permitted daily exposure limits (PDEs), and other health-based exposure limits (HBELs).
This position will support programs across Takeda’s therapeutic areas and across all stages of development from early discovery to marketed products. The assessments will span Takeda’s core modalities.
In this role the candidate is expected to be able to work with minimal supervision on data collection, storage, and analysis supporting toxicology product risk assessments and to become familiar with regulatory guidance documents and industry trends as they relate to these assessments that support EHS, PharmSci, and manufacturing activities. The person must be scientifically independent and able to articulate implications and risks from toxicology assessments to a broad audience.
How You Will Contribute
Collection and curation of data supporting toxicology risk assessments from external and internal sources (including review, updating, and harmonization of existing internal databases/sources into a new central repository)Provide support to toxicology product risk assessments for impurities, extractable and leachable, and in silico mutagenicity assessments for drug manufacturing functionsProvide toxicology components of PDEs, occupational exposure limits (OELs) and other HBELs in support of EHS interfaceInternship Development Opportunities:
You will gain familiarity with relevant regulations and guidance documents pertaining to pharmaceutical development. Significant exposure to cross-functional and global collaborations.Familiarity with state of the science software used to generate in silico toxicological predictions as well as to store and manage toxicological data. Gain understandings of relevant frameworks for establishing exposure limits to protect worker and patient populations as well as the environment.Job Requirements:
This position is a remote positionUndergraduate, Graduate, PhD, MD student with completion of a minimum of one year of university studies.Exceptional interpersonal, verbal communication and writing skills.Deadline-driven with an elevated level of organizational and planning skills.Strong quantitative, analytical, problem solving and conceptual skills.Proven record of accomplishment of teamwork, adaptability, innovation, initiative, and integrity.Global mindset to grow in a diverse work environment.Previous experience in a pharmaceutical setting providing toxicology risk assessments is a plusInternship Eligibility
Must be authorized to work in the U.S. on a permanent basis without requiring sponsorshipMust be currently enrolled in a degree program graduating December 2025 or laterThe internship program is 10-12 weeks depending on the two start dates (June 2nd- August 29th) or (June 16th - August 22ndThe intern must be able to commit to one of these time framesAble to work full time 40 hours a week during internship datesTakeda does not provide a housing stipend or relocation support for the U.S Summer Internship ProgramProgram Highlights:
Hands-on experience with real projects and responsibilitiesDedicated mentorship program pairing interns with experienced professionalsNetworking opportunities with industry professionals and fellow internsInternship events focused on professional and skills developmentExposure to multiple business areas or departments within a Pharmaceutical OrganizationApplications will be accepted between December 18th and January 12th
Takeda Compensation and Benefits Summary
We understand compensation may be an important factor as you consider an internship opportunity. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Massachusetts - VirtualU.S. Hourly Wage Range:
$21.00 - $46.00
The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate’s school year/level to be entered following completion of internship. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. internship benefits vary by location and may include:
Paid sick time
Civic Duty paid time off
Participation at company volunteer events
Participation at company sponsored special events
Access to on-site fitness center (where available)
Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking.
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.
LocationsMassachusetts - VirtualWorker TypeEmployeeWorker Sub-TypePaid Intern (Fixed Term) (Trainee)Time TypeFull timeJob Exempt
No