ZipRecruiter

Log In

1

Pharmaceutical Technical Writer Jobs (NOW HIRING)

CEDENT

Technical Writer

Springfield, NJ

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 ...

Digital Prospectors

Technical Writer

Houston, TX

Support documentation activities related to fill/finish manufacturing processes Qualifications: * 5-8 years of Technical Writing experience within the pharmaceutical or biotech industry * Strong ...

AST

Technical Writer

Tacoma, WA · On-site

$30.83 - $43.27/hr

The Technical Writer will play an active role in developing, maintaining, and standardizing technical documentation that supports AST's pharmaceutical equipment, systems, and internal processes. This ...

AST

Technical Writer

Tacoma, WA · On-site

$30.83 - $43.27/hr

The Technical Writer will play an active role in developing, maintaining, and standardizing technical documentation that supports AST's pharmaceutical equipment, systems, and internal processes. This ...

ProSidian Consulting

Technical Writer

Charlotte, NC · Remote

... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... ProSidian Seeks a Technical Writer (Contract Contingent) in Charlotte, NC / Remote to support an ...

Aequor

Technical Writer

Swiftwater, PA · On-site

... pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred Proficiency in ... technical writer is responsible for supporting on-time implementation of OneLIMS EM global system ...

ICONMA

Technical writer

Lake Forest, IL

Specialist/Technical Writer Location: Lake Forest, IL Duration: 4 months Description: Primary ... writing pharmaceutical/medical documentation (e.g. batch records, specifications, procedures ...

ZERO ZONE INC

Technical Writer

North Prairie, WI

We also make powerful industrial refrigeration systems for food warehousing, pharmaceuticals, and ... Under the direction of the Director of Marketing & National Accounts, the Technical Writer will be ...

Zero Zone, Inc

Technical Writer

North Prairie, WI · On-site

$55K - $65K/yr

We also make powerful industrial refrigeration systems for food warehousing, pharmaceuticals, and ... Under the direction of the Director of Marketing & National Accounts, the Technical Writer will be ...

next page

Showing results 1-20

People also search for

All JobsPharmaceutical Technical Writer Jobs

Pharmaceutical Technical Writer information

See salary details

$13

$38

$66

How much do pharmaceutical technical writer jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for pharmaceutical technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

How much does a technical writer make at Pfizer?

A pharmaceutical technical writer at Pfizer typically earns between $70,000 and $100,000 annually, depending on experience, education, and location. The role often requires knowledge of regulatory documentation, scientific writing skills, and familiarity with pharmaceutical industry standards.

Is technical writer a high paying job?

A pharmaceutical technical writer can earn a competitive salary, often higher than other technical writing roles due to industry specialization and regulatory knowledge. Salaries vary based on experience, education, and location, with advanced skills in drug development, regulatory compliance, and scientific writing increasing earning potential.

How much does a Sanofi technical writer make?

A pharmaceutical technical writer at Sanofi typically earns between $70,000 and $110,000 annually, depending on experience, location, and education. The role requires strong writing skills, knowledge of regulatory standards, and familiarity with pharmaceutical documentation processes.

How does a Pharmaceutical Technical Writer typically collaborate with scientists and regulatory teams during document preparation?

Pharmaceutical Technical Writers work closely with scientists, researchers, and regulatory affairs teams to ensure that all documentation—such as clinical study reports, regulatory submissions, and standard operating procedures—is accurate, clear, and compliant with industry standards. Collaboration often involves attending meetings to discuss project requirements, clarifying scientific data with subject matter experts, and incorporating feedback from multiple stakeholders. This cross-functional teamwork is essential for producing high-quality documents that meet both scientific rigor and regulatory expectations.

What is the difference between Pharmaceutical Technical Writer vs Pharmaceutical Regulatory Affairs Specialist?

AspectPharmaceutical Technical WriterPharmaceutical Regulatory Affairs Specialist
CredentialsBachelor's in life sciences or related field; writing certifications helpfulBachelor's in life sciences, law, or related; regulatory certifications preferred
Work EnvironmentPharmaceutical companies, CROs, biotech firmsRegulatory agencies, pharmaceutical companies, consulting firms
Industry UsageCreating SOPs, clinical trial documents, product labelsPreparing submissions, ensuring compliance, liaising with authorities
Search/Comparison IntentUnderstanding roles, career paths, required skillsRegulatory processes, compliance, documentation requirements

The Pharmaceutical Technical Writer focuses on creating clear, accurate documentation such as SOPs and clinical reports, while the Pharmaceutical Regulatory Affairs Specialist handles regulatory submissions and compliance. Both roles require strong knowledge of pharmaceutical processes, but their primary responsibilities and work environments differ.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Technical Writer, and why are they important?

To thrive as a Pharmaceutical Technical Writer, a background in life sciences, strong writing skills, and knowledge of regulatory requirements are essential, often supported by a relevant degree. Familiarity with document management systems, regulatory submission tools, and industry-specific style guides like ICH or EMA guidelines is typically required. Attention to detail, ability to synthesize complex information, and strong collaboration skills help individuals excel in this role. These skills ensure accuracy, compliance, and clarity in documentation critical for regulatory approval and safe pharmaceutical development.

What is technical writing in pharma?

Technical writing in pharma involves creating clear, accurate documentation such as standard operating procedures, regulatory submissions, and clinical trial reports to ensure compliance and effective communication within the pharmaceutical industry. Pharmaceutical technical writers must understand scientific concepts and often use tools like document management systems and style guides to produce precise content. Strong attention to detail and knowledge of regulatory requirements are essential for this role.

What does a Pharmaceutical Technical Writer do?

A Pharmaceutical Technical Writer creates clear, accurate, and compliant documentation related to pharmaceutical products and processes. This includes writing and editing regulatory submissions, standard operating procedures (SOPs), clinical study reports, manufacturing instructions, and other technical documents. Their work ensures that complex scientific information is communicated effectively to regulatory authorities, healthcare professionals, and internal stakeholders. They must have a strong understanding of scientific concepts, regulatory guidelines, and industry standards to produce high-quality documentation.
More about Pharmaceutical Technical Writer jobs
What cities are hiring for Pharmaceutical Technical Writer jobs? Cities with the most Pharmaceutical Technical Writer job openings:
What states have the most Pharmaceutical Technical Writer jobs? States with the most job openings for Pharmaceutical Technical Writer jobs include:
What job categories do people searching Pharmaceutical Technical Writer jobs look for? The top searched job categories for Pharmaceutical Technical Writer jobs are:
Pharmaceutical Technical Writer jobs near you
Infographic showing various Pharmaceutical Technical Writer job openings in the United States as of June 2026, with employment types broken down into 23% As Needed, 34% Full Time, 28% Part Time, 11% Temporary, and 4% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.
Pharmaceutical Technical Writer

Pharmaceutical Technical Writer

ProStaff Solutions Inc

New Brunswick, NJ • On-site

Other

Posted 5 days ago

Job description

Are you looking to be a part of a growing pharmaceutical company? One of our largest clients is currently seeking a Pharmaceutical Technical Writer to join their New Brunswick, New Jersey 08901 team. Our client is one of the leading pharmaceutical companies specializing in developing and manufacturing solid dosage products. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Full-time Onsite
Direct Hire
Pay Rate: DoE
Job summary:
Perform investigation's and assist manufacturing and packaging operations on investigations, Product quality complaints. Assist in cross functional investigations for out of specification (OOS), out of trend (OOT), Laboratory Events, CAPAs, and change controls.

Areas of responsibility:
  • Ensure timely closure of all manufacturing/packaging and Quality Management System records.
  • Organize and participate in and reviews of cross functional investigation's
  • Represents Operations at cross-functional meetings.
  • Work with process owners and SMEs to implement agreed upon procedural documentation and to develop cross-functional process models
  • Collect input from stakeholders and consolidate comments for conflict resolution
  • Drive the improvement in established KPI's / metrics for manufacturing and packaging departments
  • Assist operations in responses to any internal audit, corporate audit, or regulatory audit observations involving manufacturing or packaging Control.

Travel Estimate: Up to 5%
Required Qualifications:
  • Associate degree in Life Sciences, Pharmacy, or equivalent required.
  • Minimum of three (3)years working in a pharmaceutical environment with at least two (2) years of experience within manufacturing area.
  • Demonstrated excellent communication: verbal, written and presentation skills.
  • A self-starter with a hands-on approach and a can-do attitude.
  • A team building champion driving innovative cross functional synergies.
  • Excellent project management and problem solving skills.
  • Excellent computer skills; MS Office (Word, Excel, PowerPoint), Track wise, EDMS, Outlook.
  • Knowledge of GDP, GMP, QA Documentation, QA Batch records, Quality Systems, Archiving, Retrieval, EDMS workflow, Document Life Cycle and Audit Compliance.
  • The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).

Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.
About ProStaff Workforce Solutions
We are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaff Workforce Solutions is a group of industry experts-many hailing from larger agencies-who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates.
Our Values
Integrity
Commitment
Quality
Diversity
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.
#IND1


Apply