Top 17 Technical writer Jobs in Edison, Nj

Manufacturing Technical Writer
Celltrion Branchburg, LLC —Branchburg, NJ
- $71,250 - $116,000 a year
- Full-time
- Mid-level
- Continuous improvement
- Travel
- Paid holidays
- Disability insurance
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5d
Technical Writer - Operations
Experic LLC —Cranbury, NJ
- $80,000 - $110,000 a year
- Mid-level
- Office
- 3 years
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Technical Writer
CEDENT —Springfield, NJ
- Microsoft Excel
- Mid-level
- Analysis skills
Documentation and Training Specialist
Princeton Plasma Physics Laboratory —Princeton, NJ
- $93,400 - $149,200 a year
- Full-time
- Mentoring
- Senior level
- Associate's degree
- On-the-job training
Lead Content Writer
Cognizant —Somerset, NJ
- $95,000 - $115,000 a year
- Full-time
- Hybrid work
- Writing skills
- Mentoring
- Senior level
- Paid parental leave
- Employee stock purchase plan
2d
Technical Writer
Marotta Controls, Inc. —Parsippany-Troy Hills, NJ
- $75,000 - $100,000 a year
- Engineering
- Mid-level
- Office
- Paid holidays
- Disability insurance
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Regulatory CMC Technical Writer
SOKOL GxP Services —New Brunswick, NJ
- $68,702 - $87,256 a year
- Contract
- Hybrid work
- Microsoft Excel
- Mid-level
- Bachelor's degree
- Paid holidays
- Health insurance
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Technical Operations Scientist
Lupin Pharmaceuticals Inc. —Somerset, NJ
- $70,000 - $95,000 a year
- Full-time
- Engineering
- Mid-level
- 3 years
Technical Writer
Nexagen —Township of Monroe, NJ
- $32,210 a year
- 11+ years
- Research
- Mid-level
- Health insurance
- Dental insurance
On Site Technical Writer - Union, NJ
Adaptation —Union, NJ
- $45 - $50 an hour
- Full-time
- Microsoft Excel
- 5 years
- Research
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Technical Writer
Nexagen Networks, Inc. —Township of Monroe, NJ
- $32,210 a year
- 11+ years
- Research
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Infrastructure Technical Writer
IPolarity LLC —Whippany, NJ
- Full-time
- Microsoft Word
- Computer science
- Microsoft Excel
Quick Apply
11d
Technical Writer - Berkeley Heights, NJ/Hybrid
Software Technology Inc —Berkeley Heights, NJ
- Computer Science
- Office
- Analysis skills
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Senior Medical Writer
BOLDSCIENCE —New Brunswick, NJ
- Remote
- Medicine
- Doctor of Philosophy
- Organizational skills
Engineering Technical/Tech Writer
Genesis Technical Staffing —United States
- Overtime
- Microsoft Outlook
- Military
- Mid-level
Quick Apply

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Manufacturing Technical Writer

Celltrion Branchburg, LLC
Branchburg, NJ

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Job Details

Full-time
$71,250 - $116,000 a year
5 days ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance
Retirement plan

Qualifications

Document control experience within pharmaceutical industry
Technical writing experience within manufacturing
TrackWise
Manufacturing standard operating procedures
Manufacturing facility experience
Cleanroom experience
Managing projects
Production batch record review
Standard operating procedures (SOPs)
Technical Proficiency
Cross-functional communication
Standard operating procedures drafting

Full Job Description

Celltrion is a leading biopharmaceutical company that specializes in research, development and manufacturing of innovative therapeutics. We are committed to delivering innovative and affordable medications to promote patients’ access to advanced therapies. We have been at the forefront of biotherapeutic development uncovering new ways of targeting the drivers of disease by creating next-generation biologics and small molecule products.

Celltrion Branchburg, LLC is a subsidiary of Celltrion USA, established in 2025 following Celltrion USA’s acquisition of Eli Lilly’s drug substance (DS) manufacturing facility located in Branchburg. By linking robust local manufacturing capabilities with an existing direct sales network, we aim to generate greater synergies across our operations. Looking ahead, we also anticipate expanding into the global contract manufacturing organization (CMO) sector.

Position Brand Description:

The Manufacturing Technical Writer supports the Manufacturing Process team (s) in authoring, reviewing, and approving of GMP documentation, i.e. Process Batch Records, Standard Operating Procedures (including procedures that support the execution of Electronic Batch Records) and Forms, to support the manufacture of commercial and clinical products in the BB50 Manufacturing Facility. This position plays a key role in the success of product re-introductions as well as new product introductions. This position will routinely interact

with Operators, Process Engineering, TS/MS, Quality Assurance, Quality Control and Logistics departments. Working knowledge of cGMPs, manufacturing operations and documentation support systems, such as Regulus and Trackwise is essential.

Key Objectives/Deliverables:

Manage for Results /Strategic Planning:

1. Responsible for ensuring production documentation, such as Process Batch Records, Standard Operating Procedures (including procedures that support the execution of Electronic Batch Records) and Forms, are accurate as compared to relevant Technology Transfer Documents and available for use, i.e. authored, reviewed, approved, and released, in a timely manner to support manufacturing operations.

Facilitate PmatchesP exercise as needed.

2. Ownership of the Manufacturing Document Revision Tracking Spreadsheet(s) and responsible for ensuring modifications to batch records that apply to multiple products are integrated into each applicable production process as each product is introduced/re-introduced into the facility.

3. Provide visibility of documentation review/approval schedule to Process Team and drive Process Team to meet documentation review/approval timelines.

4. Support continuous improvement efforts both from a quality and efficiency perspective by streamlining batch records and standard operating procedures as well as review and approval process.

5. Responsible for owning document related change control implementation summaries for manufacturing department as required.

6. Author, review and approve technical reports as required.

7. Subject matter expertise and execution of routing and managing documents in the controlled quality documentation system.

8. Contribute and adhere to safety, environmental, quality standards of the Corporation.

9. Provide guidance on the document revision process for the local Document Management System.

Basic Requirements:

1. Must have a technical proficiency of operations within an area and be willing to acquire technical proficiency of operations within all areas of manufacturing.

2. Must be able to write effectively as demonstrated through authorship of batch records, standard operating procedures, and observations / deviations.

3. Must exhibit a team first attitude.

4. Must possess excellent organizational, communication, interpersonal, and written skills.

5. Must be able to prioritize work, drive projects to completion and collaborate with cross functional groups to drive decisions to support documentation completion.

6. Must meet the physical requirements of the job; must have the ability to:

a. Wear appropriate clean room attire.

b. Walk down systems when writing documents to ensure completeness.

This role is exempt and the anticipated compensation for this role is $71,250 - $116,000.

This is a banded role, and candidates will be placed within the range based on experience, skills, internal equity, and market considerations.

Celltrion Branchburg, LLC offers a comprehensive benefits package that includes paid time off (holidays, vacation, and additional leave), medical, dental, and vision insurance, life insurance, a company-matched retirement savings plan, wellness programs, and short- and long-term disability benefits. This role requires up to 10% travel, on-call availability, and may involve shift work. Hybrid work flexibility may be available based on business needs; relocation assistance is not provided.

Celltrion Branchburg, LLC is proud to be Equal Opportunity Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, protected veteran status, disability, or any other legally protected status.

Quick Apply

Refine Your Search

technical writer jobs in edison, nj

Manufacturing Technical Writer

Technical Writer - Operations

Technical Writer

Documentation and Training Specialist

Lead Content Writer

Technical Writer

Regulatory CMC Technical Writer

Technical Operations Scientist

Technical Writer

On Site Technical Writer - Union, NJ

Technical Writer

Infrastructure Technical Writer

Technical Writer - Berkeley Heights, NJ/Hybrid

Senior Medical Writer

Engineering Technical/Tech Writer

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