Quality Assurance Intern jobs in United States
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Bristol Myers Squibb · 1 month ago

Quality Assurance Intern

Bristol Myers Squibb is a dynamic biotechnology company focused on improving survival of people with cancer. The Quality Assurance Intern will support QA Operations across multiple areas, ensuring compliance with regulatory standards and maintaining quality standards for radiopharmaceutical production.

BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
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Responsibilities

Assist in day-to-day QA Operations activities to ensure compliance with GMP and regulatory requirements
Support Quality disposition process by ensuring that all required documents are accurately and properly completed and compiled against approved procedures and specifications, including all related deviations
Support internal manufacturing processes through shop floor monitoring and documentation review
Participate in external manufacturing oversight activities, including review of batch records and quality documentation
Aid in incoming material release by verifying documentation and performing quality checks
Contribute to continuous improvement initiatives within QA Operations
Maintain accurate records and ensure timely completion of assigned tasks
Assist in drafting Standard Operating Procedures (SOPs), batch records, technical documents, and other document types utilized at the site
Contribute to continuous improvement initiatives by identifying opportunities to enhance process efficiency, reduce costs, or improve product quality
Maintain accurate and detailed documentation for all activities in compliance with regulatory standards
This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials
Ability to climb ladders and lift up to 50 lbs

Qualification

GMP complianceQuality assuranceAnalytical skillsMicrosoft OfficeOrganizational skillsProblem-solving skillsCommunication skillsTeam collaborationAttention to detail

Required

Current enrollment in a Bachelor's or Master's degree program in engineering, science, or a related field
Eagerness to learn and adapt in a dynamic, regulated environment
Strong organizational skills and ability to manage multiple tasks
Commitment to maintaining high standards of safety, quality, and compliance
Strong analytical and problem-solving skills with attention to detail
Proficiency in Microsoft Office
Ability to work independently and collaboratively in a team-oriented environment
Excellent written and verbal communication skills
Ability to climb ladders and lift up to 50 lbs
This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials
All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment

Preferred

Basic understanding of pharmaceutical manufacturing processes, validation principles and regulatory requirements
Prior internship or coursework in pharmaceutical manufacturing, process engineering, or quality assurance

Benefits

Medical, pharmacy, dental and vision care.
Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).
Financial well-being resources and a 401(K).
Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.
Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.
Parental, caregiver, bereavement, and military leave.
Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
Other perks like tuition reimbursement and a recognition program.

Company

Bristol Myers Squibb

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At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

Funding

Current Stage
Public Company
Total Funding
$29.32B
Key Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B

Leadership Team

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Charles Bancroft
CFO
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Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
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Company data provided by crunchbase