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Beam Therapeutics

Develops base editing–based precision medicines

Quality Co-op

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Internship · Winter 2027Durham, NC, USA$23 - $30 /hr

About the Job

Requirements

  • The candidate must be pursuing a Bachelor of Arts degree in Biotechnology, Bioengineering, Biochemistry, or a related field.
  • Prior industry internship or academic lab-based research experience is preferred.
  • The candidate should have a solid academic foundation in science and laboratory coursework, such as biology, chemistry, biochemistry, biochemical or bioengineering, microbiology, tissue culture, or molecular biology.
  • Applicants must be currently enrolled in a degree-granting college or university program and maintain student status throughout the co-op.
  • The role requires onsite attendance 4–5 days per week.

Responsibilities

  • Provide quality system expertise for external collaborations, identify solutions, and ensure compliance with Good Manufacturing Practice requirements.
  • Work with cross-functional teams, partners, and vendors to gather background knowledge needed to complete assignments.
  • Support drafting and reviewing Standard Operating Procedures and related Good Manufacturing Practice documents.
  • Participate in system improvement initiatives to optimize business processes and practices within Veeva.
  • Participate in projects that support the Quality Systems department holistically.
  • Assess document metadata within Veeva for missing data and facilitate cleanup.
  • Help organize the Document Archival Room and enter paper archives into a tracking database.
  • Assist with logbook cleanup around the site.
  • Create Person Records and assign initial learner roles.
  • Run the Veeva/SuccessFactors report and make needed changes.
  • Create micro-learning trainings for wide personnel use.
  • Create flow charts for all process areas.
  • Update document metadata for documents unassigned for product, stage, or impacted departments.
  • Assess GR records to solidify retention of all document types within the archived lifecycle.
  • Conduct periodic curriculum reviews.
  • Assist with learner-role and curriculum consolidation.
  • Support BEAM-101 and BEAM-302 supplier commercialization activities.
  • Assess authorized vendor qualification status.
  • Complete Veeva supplier qualification documentation.
  • Support reassessment of existing forms and records.
  • Identify gaps and create replacement or new assessments as required.
  • Align supplier risk assessments and vendor classifications.
  • Document commercial-readiness status.
  • Support SCN intake, assessment, tracking, and follow-up.
  • Support associated change controls.
  • Maintain visibility of aging and overdue actions.
  • Track supplier audit responses and corrective and preventive actions.
  • Follow up on overdue commitments.
  • Review supporting evidence.
  • Maintain audit records and closure documentation.

Desired Qualifications

  • Prior industry internship or academic lab-based research experience.

About the Company

Beam Therapeutics

Develops base editing–based precision medicines

Beam Therapeutics uses base editing to develop precision genetic medicines aimed at correcting disease-causing mutations. It focuses on R&D and collaborates with pharmaceutical companies and research institutions to fund and advance therapies, earning revenue through partnerships, licensing, upfront and milestone payments, and royalties. The company targets genetic disorders such as sickle cell disease with the goal of delivering lifelong cures, differentiating itself through its emphasis on durable genetic remedies and a science-driven, values-led culture.

Company size
501-1,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2017

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