Summer Intern – GMP Quality jobs in United States
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Karyopharm Therapeutics Inc. · 1 day ago

Summer Intern – GMP Quality

Karyopharm Therapeutics Inc. is seeking a Summer Intern in GMP Quality to assist with various quality-related activities. The intern will support the Quality Unit efforts, including data collection, quality investigations, and continuous improvement projects within the organization and its partners.

Health CareMedicalPharmaceutical
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Assist GMP in data collection and report generation for Annual Quality Management Review (QMR). This project will require creation of excel lists, statistical analysis, and technical writing. This will give an individual overview of drug manufacturing and testing processes along with affiliated regulations and guidelines
Assist in management of minor product quality investigations in Veeva Vault. This project will require individuals to learn and execute documentation for quality event investigations
Develop Smartsheets and trackers for GMP Quality to better manage project deliverables and timelines
Assist GMP Quality group in continuous improvement projects by participating in SOP revisions and process optimization
Maintain deviation and change control lists and assist in notification of change controls to Karyopharm’s global partners
Provide communication support for training notifications and scheduling training for Karyopharm’s business partners
Assist Quality Management Systems team with revision of the training management program including updating training matrices, creating excel of GxP processes; training requirements and required training per functional team in support of Veeva configuration updates
Support review of batch documentation and analytical data review received from CDMOs (Contract Drug Manufacturing Organizations) for various manufacturing and testing operations of Karyopharm’s product

Qualification

GMP QualityAnalytical testingQuality oversightMS Office proficiencyOral communicationWritten communicationTeam collaborationAdaptabilityMotivation

Required

Enrolled into undergraduate or graduate programs in scientific disciplines with interest to learn highly regulated drug manufacturing process, analytical testing, and quality oversight
Good Oral and Written communication skills
Highly proficient with MS Office tools
Ability to learn and adapt with ambiguity of strengths
Work in a team setting adopting collaborative and learning approach for achieving results
Enthusiasm to learn new skills and Motivation towards career development
Must be able to complete the Karyopharm Internship Program 27 May – 08 Aug 2025
Currently enrolled high school or college (bachelor's program) student
Student must be returning to school in the Fall Term
Must have a minimum GPA of 3.0
Must be highly organized and have the ability to work independently and collaboratively as a team
Clear, concise verbal & written communication

Preferred

Previous experience in Pharmaceutical or Biotech organizations is desired but not required

Company

Karyopharm Therapeutics Inc.

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Karyopharm Therapeutics Inc.

H1B Sponsorship

Karyopharm Therapeutics Inc. has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (8)
2024 (2)
2023 (10)
2022 (8)
2021 (5)
2020 (10)

Funding

Current Stage
Public Company
Total Funding
$607.2M
Key Investors
Avidity PartnersForesite CapitalDelphi Ventures
2025-10-08Post Ipo Equity· $33M
2025-10-08Post Ipo Debt· $27.5M
2022-12-05Post Ipo Equity· $165M

Leadership Team

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Brian Austad
Senior Vice President, Pharmaceutical Sciences
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Sohanya Cheng
EVP, Chief Commercial Officer & Head of Business Development
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Company data provided by crunchbase