2025 Summer Intern, Research & Development Quality - Bristol Myers Squibb
Madison, NJ
About the Job
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
This internship position in Research & Development Quality offers education and exposure across various fields, including, Non-Clinical Quality, Clinical Quality, Pharmacovigilance Quality, Quality Risk Management, and Innovative Capabilities.
Department responsibilities:
+ Non-Clinical Quality Support : Overseeing and auditing nonclinical processes from the discovery of new molecular entities through early development.
+ Clinical Quality Support: Providing trial support, data quality management, and vendor oversight for the R&D organization. Conducting audits of clinical processes, vendors, and investigator sites supporting clinical trials from Phase 1 to Phase 4 to identify areas for improvement early.
+ Post-Marketing Oversight: Ensuring independent quality oversight of Clinical and Post-Marketing Safety, Regulatory Affairs, and Medical Affairs activities throughout the product lifecycle. Conducting audits of processes, affiliate operations, and third parties supporting post-marketing safety activities.
+ Quality Risk Management: Proactively identifying and managing potential quality issues. Defining a knowledge-based, data-driven risk management methodology to generate a comprehensive risk landscape, develop predictive quality narratives, and aid decision-making.
+ Innovative Capabilities: Developing innovative capabilities to enhance the R&D Quality framework.
We are seeking a self-motivated student eager to gain real-world experience in the pharmaceutical industry. The intern will work closely with professional mentors to hone their skills and build a professional network.
Key Responsibilities
+ Assist in overseeing the quality of Non-Clinical, Clinical, Patient Safety, Regulatory Affairs, and Medical Affairs activities.
+ Evaluate the compliance of processes and policies with regulatory requirements.
+ Support the implementation of audit programs by observing and participating in audits to assess regulatory compliance.
+ Use data analytics to generate business-relevant reports.
+ Help develop and enhance audit risk tools and templates.
+ Actively participate in informal networking/mentor meetings and formal symposiums.
+ Research and present future focused advancements in R&D Quality business strategies.
+ Generate and report metrics; brainstorm on metric improvements.
+ Provide project management support, services for proof-of-concept projects, and support process design and improvement.
Qualifications & Experience
+ Candidates must be currently enrolled in an accredited university program seeking an Undergraduate (BA/BS) or Graduate degree (MA/MS/MBA/PharmD) in data science, statistics, mathematics, life sciences or health sciences.
+ Seniors graduating in Spring or Summer 2025 are eligible to apply only if they will be continuing their education for the following semester (Fall 2025).
+ Must include GPA on resume for consideration (program requires GPA of 3.0 or greater).
+ All candidates must be authorized to work in the US without sponsorship needs now or in the future.
+ Must have good oral/written communication skills and be able to work in a team environment; experience working with diverse teams.
+ Proficient in MS Office Suite; experienced in digital tools and technologies.
+ Strong organizational skills, along with attention to detail and the ability to prioritize tasks.
+ Self-starter who enjoys the challenge of working in a complex environment.
BMSEC, BMSINTERN
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1586373
Updated: 2024-10-28 03:49:58.559 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
This internship position in Research & Development Quality offers education and exposure across various fields, including, Non-Clinical Quality, Clinical Quality, Pharmacovigilance Quality, Quality Risk Management, and Innovative Capabilities.
Department responsibilities:
+ Non-Clinical Quality Support : Overseeing and auditing nonclinical processes from the discovery of new molecular entities through early development.
+ Clinical Quality Support: Providing trial support, data quality management, and vendor oversight for the R&D organization. Conducting audits of clinical processes, vendors, and investigator sites supporting clinical trials from Phase 1 to Phase 4 to identify areas for improvement early.
+ Post-Marketing Oversight: Ensuring independent quality oversight of Clinical and Post-Marketing Safety, Regulatory Affairs, and Medical Affairs activities throughout the product lifecycle. Conducting audits of processes, affiliate operations, and third parties supporting post-marketing safety activities.
+ Quality Risk Management: Proactively identifying and managing potential quality issues. Defining a knowledge-based, data-driven risk management methodology to generate a comprehensive risk landscape, develop predictive quality narratives, and aid decision-making.
+ Innovative Capabilities: Developing innovative capabilities to enhance the R&D Quality framework.
We are seeking a self-motivated student eager to gain real-world experience in the pharmaceutical industry. The intern will work closely with professional mentors to hone their skills and build a professional network.
Key Responsibilities
+ Assist in overseeing the quality of Non-Clinical, Clinical, Patient Safety, Regulatory Affairs, and Medical Affairs activities.
+ Evaluate the compliance of processes and policies with regulatory requirements.
+ Support the implementation of audit programs by observing and participating in audits to assess regulatory compliance.
+ Use data analytics to generate business-relevant reports.
+ Help develop and enhance audit risk tools and templates.
+ Actively participate in informal networking/mentor meetings and formal symposiums.
+ Research and present future focused advancements in R&D Quality business strategies.
+ Generate and report metrics; brainstorm on metric improvements.
+ Provide project management support, services for proof-of-concept projects, and support process design and improvement.
Qualifications & Experience
+ Candidates must be currently enrolled in an accredited university program seeking an Undergraduate (BA/BS) or Graduate degree (MA/MS/MBA/PharmD) in data science, statistics, mathematics, life sciences or health sciences.
+ Seniors graduating in Spring or Summer 2025 are eligible to apply only if they will be continuing their education for the following semester (Fall 2025).
+ Must include GPA on resume for consideration (program requires GPA of 3.0 or greater).
+ All candidates must be authorized to work in the US without sponsorship needs now or in the future.
+ Must have good oral/written communication skills and be able to work in a team environment; experience working with diverse teams.
+ Proficient in MS Office Suite; experienced in digital tools and technologies.
+ Strong organizational skills, along with attention to detail and the ability to prioritize tasks.
+ Self-starter who enjoys the challenge of working in a complex environment.
BMSEC, BMSINTERN
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1586373
Updated: 2024-10-28 03:49:58.559 UTC
Location: Princeton-NJ
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Source : Bristol Myers Squibb
