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Sop Technical Writer Jobs (NOW HIRING)

Linchpin Solutions Inc

Technical Writer IV

Quantico, VA · On-site

Documentation development aligns with the MSTP Quarterly Work Plan and Doctrine SOP, ensuring synchronization with Marine Corps training and doctrine development cycles. The Senior Technical Writer ...

Linchpin Solutions Inc

Technical Writer IV

Quantico, VA · On-site

Documentation development aligns with the MSTP Quarterly Work Plan and Doctrine SOP, ensuring synchronization with Marine Corps training and doctrine development cycles. The Senior Technical Writer ...

Bowhead

Technical Writer II

King George, VA · On-site

Overview Technical Writer II (H40-2026-25276) Bowhead seeks a Technical Writer II to support a ... SOP), countdown checklists and problem reports. * Ability to work independently and interface ...

Bowhead

Technical Writer III

King George, VA · On-site

Overview Technical Writer III (H40-2026-25277) Bowhead seeks a Technical Writer III to support a ... SOP), countdown checklists and problem reports. * Ability to work independently and interface ...

Cayuse Holdings

Technical Writer IV

Blackstone, VA · On-site

$68K - $93K/yr

The Work The Technical Writer IV is responsible for writing, editing, reviewing and maintaining ... SOP) and Client's standards. This position aligns with Cayuse's core values of Innovation ...

Ilitch

Technical Writer, Training

Detroit, MI · On-site

The Technical Writer partners closely with R&D, operations, and cross-functional teams to translate ... Familiarity with process documentation, SOP development, or training enablement. Working Conditions:

Cayuse Holdings

Technical Writer IV

Blackstone, VA · On-site

$68K - $93K/yr

The Work The Technical Writer IV is responsible for writing, editing, reviewing and maintaining ... SOP) and Client's standards. This position aligns with Cayuse's core values of Innovation ...

Cayuse Holdings

Technical Writer IV

Blackstone, VA · On-site

$68K - $93K/yr

The Work The Technical Writer IV is responsible for writing, editing, reviewing and maintaining ... SOP) and Client's standards. This position aligns with Cayuse's core values of Innovation ...

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All JobsSop Technical Writer Jobs

Sop Technical Writer information

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$13

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$66

How much do sop technical writer jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for sop 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.

What is the difference between Sop Technical Writer vs Standard Technical Writer?

AspectSop Technical WriterStandard Technical Writer
CertificationsOften requires knowledge of SOP development and industry standardsFocuses on general technical writing certifications (e.g., CPT, CCST)
Work EnvironmentRegulated industries like pharmaceuticals, manufacturing, or aerospaceVarious industries including IT, engineering, and software
Employer UsageCompanies needing detailed SOP documentation for complianceOrganizations requiring user manuals, guides, and technical documentation

The main difference is that Sop Technical Writers specialize in creating Standard Operating Procedures for regulated industries, emphasizing compliance and industry standards. Standard Technical Writers have a broader scope, producing various technical documents across multiple sectors. Both roles require strong writing skills, but Sop Technical Writers often need industry-specific knowledge of SOPs and regulatory requirements.

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

To excel as an SOP Technical Writer, you need strong writing, editing, and documentation skills along with a background in technical subjects or industry-specific knowledge. Familiarity with documentation tools like Microsoft Word, Adobe FrameMaker, or specialized SOP management software, as well as experience with version control systems, is typical. Attention to detail, organizational skills, and the ability to communicate complex information clearly are crucial soft skills in this role. These capabilities ensure SOPs are clear, accurate, and accessible, which enhances operational efficiency and regulatory compliance.

What are SOP Technical Writers?

SOP Technical Writers are professionals who specialize in creating, updating, and maintaining Standard Operating Procedures (SOPs) for organizations. They ensure that complex processes are documented clearly and accurately so that employees can follow them consistently. SOP Technical Writers collaborate with subject matter experts to gather information and translate it into user-friendly documentation. Their work is essential for ensuring compliance, quality control, and efficiency within various industries, including healthcare, manufacturing, and pharmaceuticals.

How do SOP Technical Writers typically collaborate with subject matter experts (SMEs) during the documentation process?

SOP Technical Writers frequently work closely with subject matter experts to gather detailed process information and ensure that standard operating procedures are accurate and comprehensive. This collaboration often involves conducting interviews, attending process walkthroughs, and reviewing draft documents together to clarify technical details. Open communication and strong interpersonal skills are essential, as writers must translate complex procedures into clear, user-friendly documentation while accommodating feedback from SMEs. Successfully managing these relationships is key to producing effective SOPs that meet regulatory and operational requirements.
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Sop Technical Writer jobs near you
Infographic showing various Sop Technical Writer job openings in the United States as of June 2026, with employment types broken down into 20% Full Time, 71% Part Time, 4% Temporary, and 5% Nights. Highlights an 61% Physical, 2% Hybrid, and 37% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Technical Writer / Manufacturing SOP Specialist (Biotech Drug Substance Operations)

Inteldot

Barceloneta, PR • On-site

Full-time

Posted 20 days ago

Job description

Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Position Overview
We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta, Puerto Rico. The selected resources will be responsible for the review, revision, optimization, and standardization of manufacturing Standard Operating Procedures (SOPs) and related controlled documentation to support operational excellence, compliance, and process efficiency initiatives at the client site. This is a fully onsite role requiring hands-on collaboration with Manufacturing, Process Engineering, Quality, Validation, and Operations personnel.
Key Responsibilities
  • Review existing manufacturing SOPs, batch records, and operational documentation for accuracy, clarity, compliance, and efficiency
  • Update and optimize procedural documentation in alignment with current manufacturing practices and regulatory requirements
  • Collaborate with Subject Matter Experts (SMEs) across Manufacturing, Quality, Engineering, and Compliance departments
  • Identify opportunities for process simplification and procedural improvements
  • Ensure documentation complies with GMP, FDA, and internal quality standards
  • Support document lifecycle activities including routing, review coordination, version control, and approvals
  • Participate in onsite meetings, walkthroughs, and process observations to capture operational requirements accurately
  • Maintain consistency in formatting, terminology, and technical writing standards across documentation packages

Required Qualifications:
  • Bachelor's degree in science, Engineering, Technical Writing, or related field preferred
  • Minimum of 3-5 years of experience in biotech, pharmaceutical, or regulated manufacturing environments
  • Strong experience reviewing and authoring manufacturing SOPs and controlled GMP documentation
  • Experience supporting Drug Substance manufacturing operations highly preferred
  • Strong technical writing, editing, and document management skills
  • Familiarity with GMP regulations, FDA compliance expectations, and documentation practices
  • Ability to interact effectively with cross-functional teams and manufacturing personnel
  • Strong attention to detail and organizational skills
  • Ability to work independently in a fast-paced manufacturing environment

Preferred Experience
  • Biologics or biotech manufacturing experience
  • Experience with document management systems (Veeva, TrackWise, MasterControl, etc.)
  • Previous experience supporting remediation, optimization, or continuous improvement initiatives
  • Bilingual (English/Spanish) preferred

Work Environment
  • Fully onsite position in Barceloneta, Puerto Rico
  • Manufacturing and operational support environment

Additional Information
  • Candidates must have prior experience supporting similar manufacturing operations and demonstrated expertise in technical writing within regulated biotech or pharmaceutical environments.

Apply