Quality and Regulatory Internship

Teal Health

Quality and Regulatory Intern supporting compliance function for Teal Health’s at-home cervical cancer screening. Assisting in eQMS migration, regulatory research, and website content review.

Posted 6/24/2026internshipSan Francisco • California • 🇺🇸 United StatesEntry LevelWebsite

About the role

Key responsibilities & impact

Assist with organizing, indexing, and mapping controlled documents, quality records, forms, templates, training records, and related metadata to support eQMS migration activities.
Compare source documents against migration trackers to identify missing records, duplicate files, version inconsistencies, obsolete references, and metadata gaps.
Support document cleanup activities, including file naming, record categorization, cross-reference checks, and preparation of migration-ready packages for QARA review.
Maintain project trackers that show migration status, open issues, responsible owners, and completion progress.
Research state-level regulatory requirements that may impact Teal Health’s telehealth, at-home sample collection, laboratory coordination, patient communication, and commercial operations.
Summarize regulatory findings in a clear, source-linked format that identifies the state, topic, requirement, applicability, risk level, and recommended next step.
Review selected Teal website pages, patient-facing content, FAQs, product descriptions, and claims against approved source materials, labeling, clinical evidence, and regulatory guidance provided by the CRQ team.
Document website review observations in a structured tracker with page links, screenshots when appropriate, issue descriptions, proposed edits, and required reviewer functions.
Support maintenance of controlled standards, guidance documents, and regulatory reference lists, including documenting publication dates, revision status, owners, and applicability.

Requirements

What you’ll need

Currently pursuing or recently completed a degree in Regulatory Affairs, Quality Assurance, Biomedical Engineering, Biology, Public Health, Health Sciences, Life Sciences, Legal Studies, Health Policy, or a related field.
Interest in medical devices, diagnostics, digital health, telehealth, women’s health, or regulated healthcare operations.
Strong written communication skills with the ability to summarize complex information clearly and accurately.
Strong attention to detail, organization, follow-through, and comfort working with trackers, spreadsheets, and controlled documents.
Basic understanding of FDA-regulated products, quality management systems, ISO 13485, 21 CFR Part 820, labeling, advertising, promotion, or healthcare compliance preferred, but not required.
Experience with Microsoft Office, Google Workspace, Adobe Acrobat, and spreadsheet-based trackers preferred.
Ability to handle confidential information with discretion and professionalism.
Ability to work independently on assigned tasks while knowing when to escalate questions or risks.
Curiosity, humility, and willingness to learn in a regulated, fast-moving startup environment.

Benefits

Comp & perks

Health insurance
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

regulatory affairsquality assurancedocument managementdata analysisFDA regulationsISO 1348521 CFR Part 820quality management systemsmetadata managementdocument cleanup

Soft Skills

written communicationattention to detailorganizationfollow-throughdiscretionprofessionalismindependencecuriosityhumilitywillingness to learn