Zohorecruit is hiring: Quality Control Medical Writing in San Francisco

San Francisco, United States

Industry Pharma/Biotech/Clinical Research

Work Experience 4-5 years

State/Province California

Country United States

Job Description

Helping design AI systems that write regulatory documents.

Deconstructing authoring/review/QC heuristics for engineers.

Evaluating AI-generated content quality and identifying edge cases.

Bridging the gap between domain expertise (medical writing) and technical product development.

Requirements
Must Have Skills for Role:

candidates MUST have at least 3 years of US-based experience in the US.

Additionally, if applicable, please explicitly state that the candidate is open to immediate relocation since these are IN-OFFICE in SF positions.

3+ years of medical writing experience in regulatory affairs.

Direct experience with CTD documents (non-clinical and CMC).

Knowledge of FDA, EMA, and ICH guidelines.

Ability to extract and document rules/logic for technical teams.

Strong QC capabilities.

Nice to Have Skills for Role:

Familiarity with structured content formats like XML or JSON.

Experience working with life sciences software tools.

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