Support clinical supply chain planning and R&D drug development processes.
Clean up SAP planning data to improve accuracy and consistency.
Develop and implement routine data validation procedures.
Manage projects and present findings to cross-functional stakeholders.
What they're looking for
Currently pursuing a Bachelor’s degree in engineering, science, or business.
Completed at least freshman year with a 3.0 or higher GPA.
Ability to work full-time on-site in Malvern, PA.
Permanent U.S. work authorization without requiring future visa sponsorship.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for TDS Clinical Supply Chain Planning Co-Op to be in Malvern, PA.
1 vacancy is currently available.
The Co-op term is six months typically from January to June, 2027 (flexible).
Full time requirement (40 hours per week) Fully On-site.
Purpose
The Clinical Supply Chain (CSC) organization within Therapeutics Development and Supply supports the global supply of clinical materials across the Research & Development and Global Medical Affairs portfolios. Its activities span clinical supply manufacturing, demand forecasting, supply planning, and global distribution.
The TDS Malvern Clinical Supply Chain Planning organization is seeking a highly motivated Co-Op to support planning operations with a focus on improving data accuracy, strengthening planning processes, and establishing sustainable data validation practices within SAP.
This opportunity provides hands-on exposure to the role of supply chain planning within R&D drug development while allowing the Co-Op to develop analytical, problem-solving, project management, and cross-functional collaboration skills.
You will be responsible
Supporting Clinical Supply Chain Planning activities and gaining exposure to supply chain processes across the R&D drug development lifecycle.
Leading planning data clean-up activities and helping improve the accuracy and consistency of planning information.
Assessing current-state SAP planning data and identifying opportunities to improve data quality.
Supporting the development and implementation of routine SAP data validation processes.
Partnering with colleagues across Clinical Supply Chain Planning and other cross-functional teams to develop solutions to real-world supply chain challenges.
Applying analytical and creative problem-solving approaches to identify process improvement opportunities.
Supporting planning process improvements that enhance efficiency, data quality, and decision-making.
Managing assigned project activities while collaborating with multiple stakeholders.
Communicating project progress, findings, and recommendations to stakeholders.
Developing and delivering a final Co-Op presentation highlighting project outcomes and learnings.
Providing additional project and planning support as needed.
Qualifications / Requirements
Completion of Undergraduate Freshman year at an accredited University is required.
Currently pursuing a Bachelor’s degree in Supply Chain Management, Chemical Engineering, Biological Engineering, Biomedical Engineering, Pharmaceutical Sciences, Biology, Chemistry, Analytical Chemistry, Biochemistry, Molecular Biology, Related business, engineering, scientific, or supply chain disciplines.
Have a cumulative GPA of 3.0 or higher, which is reflective of all college coursework.
You must not have any Summer Internship contract or other employment commitment that could interfere with the contract dates specified for this position.
Strong analytical, quantitative, and problem-solving skills.
Demonstrated process improvement mindset and interest in identifying opportunities to improve efficiency and data quality.
Ability to work with data, identify inconsistencies, and support data validation activities.
Ability to manage multiple priorities and project activities while delivering results.
Ability to work independently as a self-starter while collaborating effectively within a cross-functional team environment.
Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.
If you are under 18 years of age, you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.
Preferred Qualifications
Previous experience or familiarity with supply chain planning or related supply chain processes.
Experience working with Enterprise Resource Planning (ERP) systems, particularly SAP.
Experience working with planning systems and performing data review, validation, or clean-up activities.
Interest in pharmaceutical R&D, clinical supply chain, demand forecasting, supply planning, or clinical supply operations.
Experience or interest in process improvement and developing standardized or repeatable processes.
Strong communication and presentation skills with the ability to summarize and communicate findings effectively.
Strong project management and organizational skills.
Demonstrated leadership through academic projects, student organizations, campus programs, or community involvement.
Ineligibility for severance.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
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Required Skills
Preferred Skills
From Johnson & Johnson's public posting, laid out for reading by newgrad.ai with the wording unchanged. Check the original before you apply.
