2023 Summer Internship - Global Regulatory Strategic Sourcing
Boston, Massachusetts
2023 Summer Internship - Global Regulatory Strategic Sourcing
Job ID R0084094 Date posted Dec. 15, 2022 Location Boston, MassachusettsBy 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’sPrivacy Noticeand 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:
Global Regulatory Affairs (GRA) manages product submissions, publishing, labeling and compliance globally for all Takeda products. In GRA Strategic Sourcing, we work with agility to be at the forefront of cutting-edge innovation for sourcing all Takeda needs from a Regulatory perspective. We manage strategy for all pricing, business relationships and contract management with suppliers, as well as supplier governance and oversight as projects are implemented.
In this role, the summer intern will support a strategic project related to the implementation of the latest outsourcing model to transition from a functional service provider model to a fully-outsourced model. The intern will learn the sourcing process, contract management and supplier oversight principles for clinical research activities in the regulatory affairs space.
This will be a “hybrid” position.
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
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
Boston, MAWorker Type
EmployeeWorker Sub-Type
Paid Intern (Fixed Term) (Trainee)Time Type
Full time- Job Type Full time
- Job Level Senior
- Travel Minimal
Global Regulatory Affairs (GRA) develops and executes innovative regulatory strategies to provide life-changing therapies to patients. GRA has a strategic role in all stages of global product development and across the Takeda Enterprise.
At Takeda, we strive to provide transformational opportunities for every member of our team, and we empower our people to take charge of their futures. In an environment that fosters lifelong learning and a growth mindset, you’ll have the support you need to thrive — at work and beyond.
- Oversee regulatory activities
- Provide strategic focus
- Collaborate cross functionally
- Ensure regulatory compliance
Where You Fit In
When you join our Regulatory Affairs team, you’ll help ensure the fastest, safest path for our treatments to get to patients. With colleagues who encourage you to question everything for better outcomes, you’ll be part of a team that’s deeply involved across each therapeutic area, from candidate selection to post-marketing.
At Takeda, you’ll join an environment with the energy and flexibility of a start-up. We continue building on our 240-year history as a global biopharmaceutical leader through our innovative mindset and lean governance. Find everything you need on our Regulatory Affairs team to positively impact patients’ lives while taking strides within your own.
Our Pipeline
Our internal research capabilities and external partnerships contribute to an R&D engine that has produced exciting new molecular entities (NMEs) across our core Therapeutic Areas. Check out our pipeline and see how we’ll continue delivering a steady stream of next-generation therapies.
Learn MoreWhat We Believe In
Our values of Takeda-ism are Integrity, Fairness, Honesty and Perseverance, with Integrity as the core. These are brought to life through actions based on Patient, Trust, Reputation and Business, in that order.
Our belief in putting people first extends beyond our patients — it includes their families and communities, as well as our Takeda colleagues and their families.
We are committed to embracing our differences, valuing different perspectives, and fostering a culture of respect, inclusiveness and empowerment.
Our embedded Diversity, Equity & Inclusion (DE&I) strategy enables us to attract and retain exceptional talent, drives innovation, and helps address systemic inequalities in our communities.
-
Integrity
-
Fairness
-
Honesty
-
Perseverance
Working at Takeda
-
Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team.
-
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission.
-
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.
-
Top Workplace
Recognized for our culture and way of working, we’re one of only 15 companies to receive Top Global Employer® status for 2023.
-
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.
-
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
View All Regulatory Affairs Jobs
Search-
Lead, Data Scientist Regulatory Intelligence and Policy Research (REMOTE)
Boston, Massachusetts, Remote Regulatory Affairs Apply for Lead, Data Scientist Regulatory Intelligence and Policy Research (REMOTE) -
Senior Manager, Global Regulatory Affairs Development - GI
Cambridge, Massachusetts Regulatory Affairs Apply for Senior Manager, Global Regulatory Affairs Development - GI -
Senior Manager, China Regulatory Affairs CMC, Beijing
Beijing, China Regulatory Affairs Apply for Senior Manager, China Regulatory Affairs CMC, Beijing
Related Content
We Take Action by Focusing on Our Four Priorities
- Create an exceptional people experience
- Responsibly translate science into highly innovative, life-changing medicines and vaccines
- Protect our planet
- Unleash the power of data and digital