Top 41 Technical writer Jobs in Elizabeth, Nj

Technical Writer
CEDENT —Springfield, NJ
- Microsoft Excel
- Mid-level
- Analysis skills
Technical Docs Writer
LangChain —New York, NY
- $115,000 - $170,000 a year
- Full-time
- Remote
- 5 years
- Mid-level
- Office
- Health insurance
- Dental insurance
On Site Technical Writer - Union, NJ
Adaptation —Union, NJ
- $45 - $50 an hour
- Full-time
- Microsoft Excel
- 5 years
- Research
Quick Apply
Technical Writer
Marotta Controls, Inc. —Parsippany-Troy Hills, NJ
- $75,000 - $100,000 a year
- Engineering
- Mid-level
- Office
- Paid holidays
- Disability insurance
Quick Apply
Technical Writer
Palantir Technologies —New York, NY
- $88,000 - $122,000 a year
- Full-time
- Mid-level
- 3 years
- Children
- Commuter assistance
- Paid parental leave
Technical Writer - API Documentation
Bloomberg —New York, NY
- $130,000 - $160,000 a year
- Research
- Mid-level
- 3 years
- Paid holidays
- Disability insurance
4d
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
Quick Apply
Technical Writer
NMG Technology Services —Brooklyn, NY
- $37.00 - $44.56 an hour
- Contract
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Quick Apply
9d
Documentation Specialist/ Technical Writer
Hill Data Management —New York, NY
- Part-time
- 5 years
- Bachelor's degree
- Senior level
Senior Technical Writer
Contact Government Services, LLC —New York, NY
- $81,120.00 - $117,173.33 a year
- Full-time
- Hybrid work
- Background check
- 3 years
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Technical Writer
T-Mobile USA, Inc. —New York, NY
- $58,700 - $105,800 a year
- Full-time
- 18 years or older
- Mid-level
- Bachelor's degree
- Paid parental leave
- AD&D insurance
10d
Technical Writer
Nexagen Networks, Inc. —Township of Monroe, NJ
- $32,210 a year
- 11+ years
- Research
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Sr. Technical Writer - Hybrid
CEDENT —New York, NY
- Contract
- Organizational skills
- Senior level
- Communication skills
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
1d
Infrastructure Technical Writer
IPolarity LLC —Whippany, NJ
- Full-time
- Microsoft Word
- Computer science
- Microsoft Excel
Quick Apply
9d
Technical Operations Scientist
Lupin Pharmaceuticals Inc. —Somerset, NJ
- $70,000 - $95,000 a year
- Full-time
- Engineering
- Mid-level
- 3 years
Technical Writer & Process Improvement Analyst
Fixity Technologies LLC —Long Island City, NY
- $40 - $45 an hour
- Full-time
- Mid-level
- Office
- Analysis skills
Quick Apply
Technical Courseware Developer
Hewlett Packard Enterprise —New York, NY
- $92,700 - $187,500 a year
- Full-time
- Computer science
- Computer Science
- 5 years
Technical Writer - Berkeley Heights, NJ/Hybrid
Software Technology Inc —Berkeley Heights, NJ
- Computer Science
- Office
- Analysis skills
Quick Apply
UX Writer
Atria Physician Practice New York PC —New York, NY
- $120,000 - $180,000 a year
- 5 years
- Urgent Care
- Mid-level
- Continuing education credits
- Health insurance
Quick Apply

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technical writer jobs near elizabeth, nj

Technical Writer

CEDENT -
Springfield, NJ

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Job Details

Qualifications

Microsoft Excel
Content creation for technical audiences
Document control experience within pharmaceutical industry
Drug regulation
Technical writing experience within manufacturing
Manufacturing standard operating procedures
Bachelor's degree
Pharmaceutical company experience
Managing projects
Productivity software
Cross-functional collaboration
Cross-functional communication
Standard operating procedures drafting
Pharmaceutical manufacturing facility experience

Full Job Description

Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards. This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry.

Responsibilities:

Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines.
Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company’s quality standards, procedures, and policies.
Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained.
Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices.
Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards.
Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected.

Essential Education and Qualifications:

Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree or certification in technical writing is a plus.
Experience:
Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry.
Experience writing technical documentation, including SOPs, validation protocols, and reports.
Knowledge:
Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing.
Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint).
Skills:
Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation.
Detail-oriented with strong organizational and project management skills.
Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.

Apply Now

Refine Your Search

technical writer jobs in elizabeth, nj

Technical Writer

Technical Docs Writer

On Site Technical Writer - Union, NJ

Technical Writer

Technical Writer

Technical Writer - API Documentation

Regulatory CMC Technical Writer

Technical Writer

Documentation Specialist/ Technical Writer

Senior Technical Writer

Technical Writer

Technical Writer

Sr. Technical Writer - Hybrid

Lead Content Writer

Infrastructure Technical Writer

Technical Operations Scientist

Technical Writer & Process Improvement Analyst

Technical Courseware Developer

Technical Writer - Berkeley Heights, NJ/Hybrid

UX Writer

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