Top 66 Editing Jobs in Stamford, Ct

CMC Technical Writer
TechData Service Company, LLC —Ridgefield, CT
- $65 - $75 an hour
- Contract
- 6 years
- Master's degree
- Bachelor's degree
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3h
Document Specialist
A&Z Pharmaceutical, Inc. —Hauppauge, NY
- $50,000 - $65,000 a year
- Full-time
- Background check
- Microsoft Excel
- English
- Health savings account
- Health insurance
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9d
Analytical SME & CMC Technical Writer
TalentBurst, Inc. —Ridgefield, CT
- $50 - $55 an hour
- Contract
- Remote
- 6 years
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
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1d
Medical Writing QC Editor
Penfield Search Partners —Fairfield, CT
- Contract
- 5 years
- Senior level
- Communication skills
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Copy Editor
The Lockwood Group, LLC —Stamford, CT
- Remote
- Mid-level
- 3 years
- Bachelor's degree
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Editorial Supervisor, Market Access
The Lockwood Group, LLC —Stamford, CT
- Remote
- 5 years
- Bachelor's degree
- Senior level
Senior Consultant, Writer, Reporting Team
Deloitte —Stamford, CT
- $80,400 - $165,000 a year
- Full-time
- Remote
- 5 years
- English
- Senior level
5d
Manager, Writer, Reporting Team
Deloitte —Stamford, CT
- $88,600 - $181,900 a year
- Full-time
- Remote
- English
- 8 years
- Mentoring
5d
Part-Time Freelance Social Media Producer/Editor
Versant Media —Stamford, CT
- $250 - $300 a day
- Weekends as needed
- Remote
- 18 years or older
- Marketing
- Bachelor of Science
- Retirement plan
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Senior Editor
WWE —Stamford, CT
- Full-time
- Mid-level
- 3 years
- Project management
6d
Senior Manager 1, Program Manager and Managing Editor, Reporting Team
Deloitte —Stamford, CT
- $113,100 - $232,300 a year
- Full-time
- Remote
- English
- Research
- Continuous improvement
5d
Freelance Digital Writer - Editor
Versant Media —Stamford, CT
- Weekends as needed
- Hybrid work
- 18 years or older
- Bachelor of Science
- Mid-level
- Retirement plan
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3d
[URGENTLY HIRING] Experienced Writing Contest Tutors
Premier Plus Education —Jericho, NY
- $40 - $70 an hour
- Choose your own hours
- School experience
- Classroom
- 5 years
- Employee discount
- Flexible schedule
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Producer-Editor, Branded Video & Graphics
Versant Media —Stamford, CT
- Weekends as needed
- Hybrid work
- 18 years or older
- Bachelor of Science
- Mid-level
- Retirement plan
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14d
Content & Editorial Strategy Director
Priceline.com —Norwalk, CT
- $160,000 - $185,000 a year
- Full-time
- Hybrid work
- Office
- 8 years
- Bachelor's degree
- Disability insurance
- Health insurance
Certified Professional Coder, Charge Review and Coding Edits Specialist III
Ambulatory Medical Practices MSO, Inc —Valhalla, NY
- $31.40 - $36.06 an hour
- Full-time
- Hybrid work
- 7 years
- Senior level
- Cardiology
- Health savings account
- AD&D insurance
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Senior Content Developer
Benchmark Education Company LLC —New Rochelle, NY
- $65,000 - $95,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Microsoft Office
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Social Media Content Creator
Lo Media Agency —Tappan, NY
- $25 - $35 an hour
- Part-time
- Hospitality
- Social media management
- Mid-level
- Flexible schedule
Quick Apply
2d
Editors
Westchester Publishing Services —Danbury, CT
- Microsoft Word
- Mid-level
Analytical SME & CMC Technical Writer
Boehringer Ingelheim —Ridgefield, CT
- $50 - $55 an hour
- Contract
- 6 years
- Master's degree
- Bachelor's degree

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CMC Technical Writer

TechData Service Company, LLC -
Ridgefield, CT

Quick Apply

Job Details

Contract
$65 - $75 an hour
3 hours ago

Qualifications

FDA submissions
USP standards
Teamwork
Master's degree
ICH guidelines
Bachelor's degree
Task prioritization
Pharmaceutical company experience
Pharmaceutical analysis
Organizational skills
Chemistry, manufacturing & controls
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials

Full Job Description

Job Type: Contract
Length: 1 year (renewable)
Location: Ridgefield, CT
Pay Rate: $65 - $75/hr.
Company: Pharma/Biotech

Duties:

We are seeking an experienced Analytical Subject Matter Expert (SME) and CMC Technical Writer to support external drug substance (DS) and drug product (DP) development programs within External Alternative CMC development (EACD).

This contract role combines deep expertise in DS/DP analytical development and quality control to support ongoing DS/DP external CMC development and demonstrated familiarity of Veera RIM system and technical writing capabilities to support documentation and global regulatory submissions (e.g., IND, CTA, NDA/MAA).

The successful candidate will collaborate with internal cross-functional teams and external partners (CDMOs/CROs) to ensure scientifically robust analytical strategies and clear, compliant CMC documentation aligned with global regulatory expectations.

Key Responsibilities

Analytical Expertise

Provide scientific leadership in phase appropriate external DS/DP analytical development/QC for NCE and NCE-like (e.g., Oligonucleotide) entities, including method development, validation, transfer and lifecycle management
Contribute to development of DS/DP phase appropriate specifications and analytical control strategies in collaboration with internal and external teams
Contribute to development of DS/DP stability programs and assignment of DS retest period, DP shelf life and material holding times as needed, with internal and external teams to support FIH and following clinical trials
Independently propose or review quality agreement, SOW, study protocols/reports, batch/stability data, to support CMC deliverables in a timeline fashion.
Prepare and communicate clearly and independently technical plans, updates and deliverables as needed in the form of reports and/or presentations within the internal teams
Partner with internal teams and external vendors (CDMOs/CROs) to resolve technical challenges and quality events and ensure timely, compliant deliverables

CMC Technical Writing

Support departmental submission activities by managing documentation workflow workflow in Veeva RIM system
Demonstrated working experience in authoring, reviewing and editing (content and format) CTD Module 3 (Drug Substance and Drug Product) documents, in particular analytical related documents.
Contribute to preparation of regulatory submissions/briefings and responses to health authority inquirie

Skills:

Required

Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development of NCE and NCE-like drug substance and solid and liquid formulations.
Demonstrated working experience in regulatory submissions
Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)

Preferred

Experience in global regulatory submissions (IND, CTA, NDA, MAA)
Experience working with external manufacturing or testing partners

Key Skills

Strong organization and technical writing skills
High attention to detail and scientific rigor
Effective communication and stakeholder collaboration
Ability to manage multiple priorities in a fast-paced environment

Education:

Advanced degree (e.g., PhD) is preferred, or Master's and Bachelor's degree in Analytical Chemistry, Pharmaceutical Sciences, or related discipline

Pay: $65.00 - $75.00 per hour

Work Location: In person

Quick Apply

Refine Your Search

editing jobs in stamford, ct

CMC Technical Writer

Document Specialist

Analytical SME & CMC Technical Writer

Medical Writing QC Editor

Copy Editor

Editorial Supervisor, Market Access

Senior Consultant, Writer, Reporting Team

Manager, Writer, Reporting Team

Part-Time Freelance Social Media Producer/Editor

Senior Editor

Senior Manager 1, Program Manager and Managing Editor, Reporting Team

Freelance Digital Writer - Editor

[URGENTLY HIRING] Experienced Writing Contest Tutors

Producer-Editor, Branded Video & Graphics

Content & Editorial Strategy Director

Certified Professional Coder, Charge Review and Coding Edits Specialist III

Senior Content Developer

Social Media Content Creator

Editors

Analytical SME & CMC Technical Writer

I want to receive the latest job alert for editing in stamford, ct

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