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Pharmaceutical Technical Writer Jobs in Delaware

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

... technical writing skills with experience authoring specifications, SOPs, protocols, and investigation reports. Preferred Qualifications * Experience supporting raw material programs in pharmaceutical ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

... technical writing skills with experience authoring specifications, SOPs, protocols, and investigation reports. Preferred Qualifications * Experience supporting raw material programs in pharmaceutical ...

WuXi AppTec

QC Raw Material Scientist

Middletown, DE · On-site

... technical writing skills with experience authoring specifications, SOPs, protocols, and investigation reports. Preferred Qualifications * Experience supporting raw material programs in pharmaceutical ...

Oak St. Health

Staff Pharmacist Full Time

Dover, DE · On-site

$47.25 - $55.50/hr

Staff Pharmacist We're building a world of health around every individual -- shaping a more ... by writing the pharmacy schedule if/as directed * Maintaining relevant clinical and technical ...

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Pharmaceutical Technical Writer information

See Delaware salary details

$13

$38

$66

How much do pharmaceutical technical writer jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for pharmaceutical technical writer in Delaware is $38.98, according to ZipRecruiter salary data. Most workers in this role earn between $28.89 and $47.16 per hour, depending on experience, location, and employer.

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.

What skills and qualifications are needed to be a pharmaceutical technical writer?

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.

How does a pharmaceutical technical writer 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 popular job titles related to Pharmaceutical Technical Writer jobs in Delaware?

For Pharmaceutical Technical Writer jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Technical Writer jobs in Delaware look for?

The top searched job categories for Pharmaceutical Technical Writer jobs in Delaware are:

Pharmaceutical Technical Writer jobs near you
Infographic showing various Pharmaceutical Technical Writer job openings in Delaware as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $81,071 per year, or $39 per hour.

Chemist (Pharmaceutical Manufacturing)

Synerfac Technical Staffing

Middletown, DE

$50K - $100K/yr

Full-time

Re-posted 22 hours ago

Job description

Job Summary
The Chemist is responsible for performing chemical analyses, testing raw materials, in-process samples, finished products, and stability samples to ensure compliance with company specifications, Good Manufacturing Practices (GMP), and regulatory requirements. The role supports manufacturing operations by maintaining product quality, investigating laboratory results, and ensuring accurate documentation.
Key Responsibilities
Perform chemical analysis of raw materials, intermediates, finished products, and stability samples using approved analytical methods.
Operate, calibrate, and maintain laboratory instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, pH meters, and analytical balances.
Prepare reagents, standards, and sample solutions according to established procedures.
Review and interpret analytical data, ensuring accuracy and compliance with specifications.
Document laboratory activities in accordance with Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and company Standard Operating Procedures (SOPs).
Investigate out-of-specification (OOS), out-of-trend (OOT), and laboratory deviations as required.
Assist in method validation, method transfer, verification, and analytical troubleshooting.
Participate in laboratory investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives.
Ensure compliance with health, safety, environmental, and quality regulations.
Support internal and external audits by providing laboratory documentation and technical information.
Collaborate with Production, Quality Assurance, Validation, and Regulatory Affairs teams to resolve quality-related issues.
Maintain laboratory cleanliness, organization, and inventory of chemicals and laboratory supplies.
Qualifications:
Bachelor's degree in Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, or a related scientific discipline.
Previous experience in a pharmaceutical manufacturing or quality control laboratory is preferred.
Knowledge of GMP, GLP, FDA, ICH, and other applicable regulatory guidelines.
Experience with chromatographic and spectroscopic analytical techniques is an advantage.
Strong analytical, problem-solving, and organizational skills.
Proficiency in Microsoft Office and laboratory data management systems.
Excellent written and verbal communication skills.
Preferred Skills
Experience with HPLC, GC, FTIR, UV-Vis spectroscopy, and dissolution testing.
Familiarity with Laboratory Information Management Systems (LIMS).
Knowledge of analytical method validation and stability testing.
Ability to work independently and collaboratively in a cross-functional team.
Strong attention to detail and commitment to data integrity.
Working Conditions
Laboratory-based position within a pharmaceutical manufacturing facility.
May require shift work, overtime, or weekend work based on production requirements.
Requires the use of appropriate personal protective equipment (PPE) and adherence to laboratory safety protocols.
Key Performance Indicators (KPIs)
Timely completion of laboratory testing.
Accuracy and reliability of analytical results.
Compliance with GMP, SOPs, and regulatory requirements.
On-time completion of documentation and reports.
Successful participation in audits and quality improvement initiatives.
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About Synerfac Technical Staffing

Sourced by ZipRecruiter

Since 1987, Synerfac has served three groups, Our Clients, Our Candidates and Our Staff. We treat all three with equal importance because we recognize the synergy of success when one group succeeds, We all succeed. Synerfac is in the business of providing opportunities and adding value. We strive to create extraordinary experiences. For our clients we provide staffing services that enable them to focus on their core competencies which will add value to their businesses. For our employees we provide permanent and temporary assignments that complement their job skills and experience while providing professional and financial rewards. For our staff –we provide careers that are balanced, uplifting and carry the highest rewards by continually improving our business process. Our goal is to enhance the lives and enterprises of all those we touch to make them better off for having known us.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Cherry Hill, NJ, US

Social media

Twitter

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