at Takeda Pharmaceuticals in Montpelier, Vermont, United States
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’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:
At Takeda, we are committed to lifelong learning.
To that end, Takeda’s summer internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience to start your career or further develop in your expertise.
The summer internship program is a full-time commitment of 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities.
Project Outline:
Creates Tech writing templates for development reports and regulatory documents. Creates templates to support M1 ancillary documents across projects to support regulatory submissions. This will be done by working within teams across regulatory submission function, functional area subject matter experts, Quality, and external organizations (CDMOs & CMOs).
The candidate is preferred to have experience in pharma/biotech documentation, contributed to regulatory submissions, building databases, have good interpersonal skills, be highly organized and detail-oriented.
This position will be remote.
How you will contribute:
+ Deadline-driven with a high level of organizational and planning skills
+ Strong analytical, problem-solving, and oral and written communication skills
+ Ability to work well in teams, effectively manage projects, and present ideas clearly and concisely.
+ Global mindset to grow in a diverse work environment
+ Excellent communication and leadership skills
+ Documentation, IT, build templates, Computer. Education in Pharmaceutical Sciences, Regulatory, Pharmaceutical Quality Control, or Scientific Disciplines
Requirements / Qualifications:
As stated above, Takeda is committed to lifelong learning opportunities. To that end, our internship program is open to currently enrolled students seeking early experiences and non-traditional candidates interested in making a career change and gaining new experience.
The requirements for these two groups of candidates are specified below:
Candidates currently enrolled at an accredited university:
+ Must be authorized to work in the US without sponsorship (i.e., Takeda will not sponsor interns)
+ Must be available to work full-time (40 hours/week), within core business hours (8 AM-5 PM), for a minimum of 12 weeks during the summer months
+ Minimum GPA 3.0/4.0
+ Undergraduate, Graduate, PhD, MD student with at least one year of university studies before internship
+ Return to university for at least one semester post-internship
+ Takeda does not provide student housing or housing stipends
Non-traditional candidates not currently enrolled at university:
+ Must be authorized to work in the US without sponsorship (i.e., Takeda will not sponsor interns)
+ Must be available to work full-time (40 hours/week), within core business hours (8 AM-5 PM), for a minimum of 12 weeks during the summer months
+ Must provide a cover letter explaining why you are seeking this internship, relevant experience that makes you a good candidate, and what you hope to achieve through the experience
+ Strong preference for non-traditional candidates with some experience relevant to the desired intern role
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
Massachusetts – Virtual
Worker Type
Employee
Worker Sub-Type
Paid Intern (Fixed Term) (Trainee)
Time Type
Full time
\#LI-Remote