Technical Writer
Raritan, NJ · On-site
They are seeking a Technical Writer to curate and write content for key AS PMO programs and ... with Pharmaceutical and Application Services preferred Company : Mindlance is a Staffing and ...
Technical Writer
Raritan, NJ · On-site
They are seeking a Technical Writer to curate and write content for key AS PMO programs and ... with Pharmaceutical and Application Services preferred Company : Mindlance is a Staffing and ...
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Contract Technical Writer
Anaheim, CA · On-site
$36 - $41/hr
We are currently looking for a Contract Technical Writer to work for a leading Greater Orange ... Experience in manufacturing/product development environment in medical/pharmaceutical industries ...
Quick apply
Contract Technical Writer
Anaheim, CA · On-site
$36 - $41/hr
We are currently looking for a Contract Technical Writer to work for a leading Greater Orange ... Experience in manufacturing/product development environment in medical/pharmaceutical industries ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... Writes a variety of technical documents; design specifications, diagrams, manuals (system and end ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... Writes a variety of technical documents; design specifications, diagrams, manuals (system and end ...
... pharmaceutical industry Direct experience in GXP-compliant quality systems is preferred ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
... pharmaceutical industry Direct experience in GXP-compliant quality systems is preferred ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
... pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad range of technical ... Exceptional written and oral communication skills. -Proven ability to create strong working ...
... pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad range of technical ... Exceptional written and oral communication skills. -Proven ability to create strong working ...
Technical Writer II
San Diego, CA · On-site
Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...
Technical Writer II
San Diego, CA · On-site
Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and regulatory requirements * Three years of experience working as a technical writer. * Project ...
Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
Quick apply
Significant working experience (>6 years) in pharmaceutical/biotech CMC and analytical development ... Strong organization and technical writing skills * High attention to detail and scientific rigor
Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treatOpioidUseDisorder (OUD). Our ...
Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treatOpioidUseDisorder (OUD). Our ...
Job Summary The Junior Technical Writer supports the Senior Scientific Technical Writer with the ... pharmaceutical manufacturing facility. * Strong organizing and writing skills. * Proficiency in ...
Job Summary The Junior Technical Writer supports the Senior Scientific Technical Writer with the ... pharmaceutical manufacturing facility. * Strong organizing and writing skills. * Proficiency in ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... ProSidian Seeks a Technical Writer | Mapping Support [DOEOP075080] - DPLH Est.: 665.6 Hrs. ST | 0 ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... ProSidian Seeks a Technical Writer | Mapping Support [DOEOP075080] - DPLH Est.: 665.6 Hrs. ST | 0 ...
Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... Prior work experience in a good manufacturing practices (GMP) environment ( pharmaceutical ...
Quick apply
Technical Writer SwiftWater, PA - Onsite 9+ Months Role will work with a team on a new digital ... Prior work experience in a good manufacturing practices (GMP) environment ( pharmaceutical ...
Bachelor s degree in Science, Communications, or English, with at least 2 years related experience in technical writing, preferably in a pharmaceutical or related environment AS in Communications or ...
Bachelor s degree in Science, Communications, or English, with at least 2 years related experience in technical writing, preferably in a pharmaceutical or related environment AS in Communications or ...
Background: BS or MS degree in arts or sciences 4+ years of technical writing experience Experience in change management Experience in medical, pharmaceutical, or other FDA regulated environment ...
Background: BS or MS degree in arts or sciences 4+ years of technical writing experience Experience in change management Experience in medical, pharmaceutical, or other FDA regulated environment ...
Technical Writer II
Swiftwater, PA · On-site
Job Summary : eTeam is seeking a Technical Writer II to support the implementation of the OneLIMS ... pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred • Proficiency in ...
New
Technical Writer II
Swiftwater, PA · On-site
Job Summary : eTeam is seeking a Technical Writer II to support the implementation of the OneLIMS ... pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred • Proficiency in ...
New
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... The Technical Writer - Level III plays an integral role by effectively participating in day to day ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... The Technical Writer - Level III plays an integral role by effectively participating in day to day ...
Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our ...
Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our ...
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
The Junior Technical Writer supports the Senior Scientific Technical Writer with the preparation of ... in a pharmaceutical manufacturing facility. • Strong organizing and writing skills. • ...
The Junior Technical Writer supports the Senior Scientific Technical Writer with the preparation of ... in a pharmaceutical manufacturing facility. • Strong organizing and writing skills. • ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... Seeking Technical Writer candidates with relevant Environmental Management Sector Experience ...
... Pharmaceuticals, Banking & Financial Services, Transportation, Federal and State Government ... Seeking Technical Writer candidates with relevant Environmental Management Sector Experience ...
Pharmaceutical Technical Writer information
See salary details
$13.70 - $18.47
2% of jobs
$18.47 - $23.23
7% of jobs
$23.23 - $27.99
12% of jobs
$29.11 is the 25th percentile. Wages below this are outliers.
$27.99 - $32.76
16% of jobs
The median wage is $36.33 / hr.
$32.76 - $37.52
17% of jobs
$37.52 - $42.29
14% of jobs
$45.38 is the 75th percentile. Wages above this are outliers.
$42.29 - $47.05
11% of jobs
$47.05 - $51.81
10% of jobs
$51.81 - $56.58
5% of jobs
$56.58 - $61.34
3% of jobs
$61.34 - $66.11
3% of jobs
$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?
| Aspect | Pharmaceutical Technical Writer | Pharmaceutical Regulatory Affairs Specialist |
|---|---|---|
| Credentials | Bachelor's in life sciences or related field; writing certifications helpful | Bachelor's in life sciences, law, or related; regulatory certifications preferred |
| Work Environment | Pharmaceutical companies, CROs, biotech firms | Regulatory agencies, pharmaceutical companies, consulting firms |
| Industry Usage | Creating SOPs, clinical trial documents, product labels | Preparing submissions, ensuring compliance, liaising with authorities |
| Search/Comparison Intent | Understanding roles, career paths, required skills | Regulatory 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:
Job description
Job Summary:
Mindlance is a national recruiting company specializing in the Life Sciences, IT, and Financial Services sectors. They are seeking a Technical Writer to curate and write content for key AS PMO programs and initiatives, including the AS Portfolio Playbook and AS Service Catalog, while collaborating with various stakeholders to create customer-friendly content.
Responsibilities:
• Lead the development of the AS Portfolio Playbook, which will educate AS employees regarding key AS Portfolio Processes.
• Lead the development of content within the AS Service Catalog content, which enables AS customers to review examples of successful AS service engagements and read service descriptions.
• In addition to writing content, partnering with Service Owners to create customer-friendly service descriptions may provide opportunities to influence the strategy and design of services.
• The candidate will organize additional content and communications for the AS PMO.
• This includes the PMO Newsletter, Best Practice Documentation, and Process Reference Guides.
• The candidate will need to collaborate with team members and stakeholders to collect, organize, curate, and publish content.
Qualifications:
Required:
• College degree in journalism, communications, or related discipline, or equivalent combination of education and experience required
• Strong verbal communication and writing skills required
• Ability to conduct independent research required
• Excellent attention to detail and proofreading skills to ensure accurate, error-free work
• High level of computer literacy and knowledge, including Microsoft Office products
• Ability to work under pressure, meet deadlines, and take critiques as needed
• Ability to understand the IT operational model and PMO processes of demand, financial, resource, benefit and service management.
• Excellent oral communications and interpersonal skills
Preferred:
• Prior experience with Pharmaceutical and Application Services preferred
Company:
Mindlance is a Staffing and Recruiting company which provides multi-vertical staffing services Founded in 1999, the company is headquartered in Union, USA, with a team of 1001-5000 employees. The company is currently Late Stage.
Mindlance is a national recruiting company specializing in the Life Sciences, IT, and Financial Services sectors. They are seeking a Technical Writer to curate and write content for key AS PMO programs and initiatives, including the AS Portfolio Playbook and AS Service Catalog, while collaborating with various stakeholders to create customer-friendly content.
Responsibilities:
• Lead the development of the AS Portfolio Playbook, which will educate AS employees regarding key AS Portfolio Processes.
• Lead the development of content within the AS Service Catalog content, which enables AS customers to review examples of successful AS service engagements and read service descriptions.
• In addition to writing content, partnering with Service Owners to create customer-friendly service descriptions may provide opportunities to influence the strategy and design of services.
• The candidate will organize additional content and communications for the AS PMO.
• This includes the PMO Newsletter, Best Practice Documentation, and Process Reference Guides.
• The candidate will need to collaborate with team members and stakeholders to collect, organize, curate, and publish content.
Qualifications:
Required:
• College degree in journalism, communications, or related discipline, or equivalent combination of education and experience required
• Strong verbal communication and writing skills required
• Ability to conduct independent research required
• Excellent attention to detail and proofreading skills to ensure accurate, error-free work
• High level of computer literacy and knowledge, including Microsoft Office products
• Ability to work under pressure, meet deadlines, and take critiques as needed
• Ability to understand the IT operational model and PMO processes of demand, financial, resource, benefit and service management.
• Excellent oral communications and interpersonal skills
Preferred:
• Prior experience with Pharmaceutical and Application Services preferred
Company:
Mindlance is a Staffing and Recruiting company which provides multi-vertical staffing services Founded in 1999, the company is headquartered in Union, USA, with a team of 1001-5000 employees. The company is currently Late Stage.
About Mindlance
Sourced by ZipRecruiter
Mindlance is a multinational staffing and services firm based in the Greater NYC area. We have 14 offices across the United States, Canada, and India. We match talented people to Fortune 500 and Fortune 1000 companies across industries. We have been in business since 1999 and are recognized by Staffing Industry Analysts (SIA) as one of the fastest-growing U.S. staffing firms. Our rapid growth means more jobs, more projects, and more opportunities for you. Our core philosophy means that you work with an organization that truly values and recognizes you.
Industry
Recruiting and staffing services
Company size
1,001 - 5,000 Employees
Headquarters location
Union, NJ, US
Year founded
1999