Top 89 Development editor Jobs in California

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —San Francisco, CA
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
12d
Editor
Untold Studios —Los Angeles, CA
- $95,000 - $160,000 a year
- Hybrid work
- Public speaking
- Mid-level
- Budgeting
E-Learning and Publications Editor
American Academy of Ophthalmology Inc —San Francisco, CA
- $102,824 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- 3 years
- Commuter assistance
- Health savings account
Quick Apply
Editor, Consumer Industry
Deloitte —San Diego, CA
- $88,600 - $163,100 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
PROOFREADER
Office of Legislative Counsel —Sacramento County, CA
- $5,774 - $5,947 a month
- Overtime
- Hybrid work
- English
- Mid-level
- Office
- Paid holidays
- Disability insurance
Editor
TrueShort —California
- $250 - $350 a day
- Full-time
- Hybrid work
- Mid-level
Quick Apply
Catalog Editor/Curriculum Analyst
California State University —East Bay, CA
- Full-time
- Background check
- Word processing
- Mid-level
- Paid holidays
- Health insurance
Content Writer/Editor
SIMON WIESENTHAL CENTER —Los Angeles, CA
- $75,000 - $80,000 a year
- Full-time
- English
- Mid-level
- 4 years
Staff Editor
Conde Nast —San Francisco, CA
- $80,000 - $105,000 a year
- Full-time
- Mid-level
- Office
- 2 years
Technical Editor and Writer Level 3/4
Northrop Grumman —Sunnyvale, CA
- $73,900 - $160,200 a year
- Overtime
- Mid-level
- Office
- 3 years
- Paid holidays
- Disability insurance
Web Content Editor
Growth Rocket —Los Angeles, CA
- Management
- English
- Research
Editor
Company3 —Santa Monica, CA
- $35 - $45 an hour
- Overtime
- Mid-level
- Office
- Travel
- Health insurance
- Paid time off
Technical Writer and Editor
General Atomics —Poway, CA
- $73,700 - $128,780 a year
- Extended hours
- Hybrid work
- 6 years
- English
- Research
- Relocation assistance
Senior Editor, Publications
SFMOMA —San Francisco, CA
- $90,000 - $95,000 a year
- Full-time
- Hybrid work
- 7 years
- Office
- Master's degree
- Commuter assistance
- AD&D insurance
Quick Apply
Technical Writer/Editor
General Atomics —Poway, CA
- $56,820 - $96,015 a year
- Extended hours
- Hybrid work
- Computer literacy
- Research
- Mid-level
- Relocation assistance
KPBS News Editor
San Diego State University Research Foundation —San Diego, CA
- $7,500.00 - $8,750.34 a month
- Weekends as needed
- Hybrid work
- Background check
- Spanish
- Mid-level
- Health insurance
- Dental insurance
4d
Manager, Editor, Government and Public Services (GPS)
Deloitte —San Diego, CA
- $88,600 - $163,100 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- English
AI Music Composer & Editor
TrueShort —California
- $200 - $450 a week
- Full-time
- Hybrid work
- Mid-level
Quick Apply
7d
Senior Editor
The Huntington —San Marino, CA
- $85,000 - $95,000 a year
- Full-time
- 5 years
- Office
- Organizational skills
- 403(b) matching
- Health insurance
[WEBTOON] Editor
WEBTOON Entertainment Inc. (Wattpad & WEBTOON Family of Brands) —El Segundo, CA
- $75,000 - $95,000 a year
- Full-time
- 3 years
- Mentoring
- Organizational skills
- Commuter assistance
- Health insurance
Quick Apply

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Regulatory Writer and/or Regulatory QC/ Editor

Vir Biotechnology -
San Francisco, CA

Quick Apply

Job Details

$90 - $120 an hour
12 days ago

Qualifications

Bachelor's degree

Full Job Description

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.

Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.

We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.

THE OPPORTUNITY

Vir Biotechnology is looking for a Regulatory Writer (Temporary) who will support the quality, consistency, and accuracy of regulatory documents produced by the Regulatory Writing team by either functioning as a support author and/or by focusing on editorial and QC review of documents written by other team members. Reporting to the Senior Director, Regulatory Writing, you will help ensure accuracy, compliance, and consistency of regulatory submission materials by partnering closely with medical writers, regulatory affairs, clinical, biostatistics, and other cross‑functional stakeholders.

WHAT YOU'LL DO

In partnership with an experienced lead author, write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, and components of regulatory submission dossiers (eg, NDA, IND, MAA)
Perform independent QC reviews of documents produced by the regulatory writing function
Verify the accuracy and internal/external consistency of documents versus their source materials
Define and confirm the scope of QC activities with document authors; identify required source documents/data and ensure availability prior to QC start
Review documents for adherence to applicable style guides (eg, AMA Manual of Style and internal style/formatting standards), templates, and regulatory guidance, identify and document discrepancies and recommended corrections
Proofread and copyedit text to ensure clarity, grammar, spelling, punctuation, and consistency of messaging/presentation, while preserving scientific and regulatory accuracy
Support preparation and inspection‑readiness of technical documents for global regulatory submissions (eg, eCTD/CTD), including integration of narrative text, tables, graphs, charts, and statistical output
Communicate QC findings clearly and constructively to medical writers and other stakeholders; collaborate to resolve issues and support timely completion of deliverables
Facilitate the efficient project management of individual document workflows (from KOM through handoff to publishing) and contribute to departmental trackers and integrated timelines. Communicate status and progress to stakeholders, participating in cross-functional meetings when needed
Contribute to the continuous improvement of QC tools, checklists, and processes; provide feedback on SOPs, work instructions, and best practices for regulatory document quality

WHO YOU ARE AND WHAT YOU BRING

Bachelor's degree and 5 plus years of relevant experience. Advanced degree in science or medical field is a plus
Working knowledge of the industry and content of key eCTD documents, familiarity with CTD/eCTD structure and common templates
Understanding of drug development and regulatory submission processes, including familiarity with ICH guidelines and major health authority expectations (eg, FDA, EMA)
Exceptional attention to detail with strong analytical and critical‑thinking skills, including the ability to identify inconsistencies, data issues, and deviations from standards
Proven ability to manage multiple tasks and priorities in a deadline‑driven environment, operating with a high degree of independence and accountability
Experience working cross‑functionally in collaborative team environments and building effective working relationships with authors, reviewers, and project teams
Experience with electronic document management and publishing systems (eg, Veeva Vault)
Experience with project and timeline management systems (eg, SmartSheet)

#LI-AS1

#LI-Remote

WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $90.00 to $120.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.

This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.

Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.

For hires based in the United States, Vir Biotechnology, participates in E-Verify.

Candidate Privacy Notice

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Refine Your Search

development editor jobs in california

Regulatory Writer and/or Regulatory QC/ Editor

Editor

E-Learning and Publications Editor

Editor, Consumer Industry

PROOFREADER

Editor

Catalog Editor/Curriculum Analyst

Content Writer/Editor

Staff Editor

Technical Editor and Writer Level 3/4

Web Content Editor

Editor

Technical Writer and Editor

Senior Editor, Publications

Technical Writer/Editor

KPBS News Editor

Manager, Editor, Government and Public Services (GPS)

AI Music Composer & Editor

Senior Editor

[WEBTOON] Editor

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