Formatter and Proofreader job in Philadelphia, PA
Philadelphia, PA CorTech LLC
| Job Ref: | 367461 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 36.00/Per Hour |
| Remote: | No |
Location |
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| City: | Philadelphia, PA |
| Post Code: | 19019 |
| Map: |
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Description |
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JobsRUs.com is seeking to hire a Formatter and Proofreader for our client! Benefits Available! Weekly Pay! Remote Position! Pay Rate - $30-40/hr Up to 20 hours per week Job Description We are seeking a detail-oriented Formatter and Proofreader with experience in regulatory documentation and scientific formatting to support our tobacco-related FDA submissions. The ideal candidate will have a strong background in preparing technical and scientific documents for submission to regulatory agencies and academic journals, with a focus on consistency, clarity, and formatting precision. Key Responsibilities: Proofread regulatory application sections to ensure: Narrative and structural consistency across sections Correct grammar, punctuation, and spelling Adherence to internal ALCS style guides and formatting standards Format documents using software tools (e.g., Microsoft Word) to meet regulatory and scientific publishing requirements Utilize and manage tools such as Starting Point, EndNote, and SharePoint for version control, referencing, and collaboration Convert reference articles and citations into final publishable formats consistent with target journal or regulatory submission specifications Ensure formatting of scientific documents complies with journal submission requirements Coordinate with regulatory, scientific, and editorial teams to maintain consistency across complex document packages Required Qualifications: 5+ years of experience in proofreading and formatting technical or regulatory documents Strong command of grammar, punctuation, and technical editing best practices Proficient in Starting Point, EndNote, and SharePoint Prior experience working on FDA regulatory submissions, preferably in tobacco-related projects Familiarity with scientific document standards and manuscript preparation for academic publishing Exceptional attention to detail and ability to meet tight deadlines Preferred Qualifications: Experience in regulated industries (e.g., pharmaceuticals, life sciences, public health) Previous work with FDA Center for Tobacco Products (CTP) documentation Background in medical writing, scientific communication, or publishing | |
ref: (367461)
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