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Sop Writer Jobs in Raleigh, NC (NOW HIRING)

Alcami Corporation

Sr. Validations Specialist

Morrisville, NC · On-site

$77K - $106K/yr

Specific responsibilities include reviewing SOP's, composing/revising SOP's and validation master ... Strong communication skills (oral and written). * Strong mechanical skills. * Strong working ...

Walmart

(USA) Pharmacy Manager, Store # 04499

Zebulon, NC · On-site

$112K - $197K/yr

... SOP QA policies standards and procedures Ensures adherence to proper policies and procedures for ... patient perceived Writes timely and effective plans of action focused on identification and ...

Aequor Inc

Animal Technician

Durham, NC · On-site

All work assignments will be performed in accordance with SOP's and protocol instructions. Must ... Excellent communication skills both written and oral. Job qualifications: * Education - AA degree ...

Aequor Technologies

Animal Technician

Durham, NC · On-site

All work assignments will be performed accordance with SOP's and protocol instructions. Must ... both written and oral. Job Qualifications • Education - degree required • Experience - Lab ...

AllSTEM Connections

Laboratory Technician

Durham, NC · On-site

$72K/yr

Conduct testing per written SOP. Organize data collection. Ability to carry out tasks through multiple process steps, testing, and data reporting. Work Hours M-F 8 hours/ day ( flex time) Equal ...

Globex IT Solutions INC

Lead Clinician

Raleigh, NC · On-site

Responsible for conducting written, standardized clinical chart reviews on each of the 8 clinical team members on a monthly basis to ensure strict adherence to state, federal, and NCNG SOP ...

Kryosphere

Be Seen First

Biorepository Technician I

Cary, NC · On-site

$18 - $22/hr

Demonstrates compliance with all Kryosphere SOP's, administrative policies & procedures, and ... Demonstrate the ability to communicate written and verbal scientific and clinical information.

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Sop Writer information

See Raleigh, NC salary details

$11

$33

$56

How much do sop writer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for sop writer in Raleigh, NC is $33.44, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $40.48 per hour, depending on experience, location, and employer.

What is an SOP writer?

A SOP (Standard Operating Procedure) Writer is responsible for creating clear, concise, and structured documents that outline procedures and best practices for an organization. They work closely with subject matter experts to ensure accuracy and compliance with industry standards. SOP Writers are commonly employed in industries such as healthcare, pharmaceuticals, manufacturing, and IT to document workflows and improve efficiency. Strong writing skills, attention to detail, and knowledge of regulatory requirements are essential for this role.

How to become a Sop writer?

To become a SOP (Standard Operating Procedure) writer, develop strong writing and technical skills, often through a degree in a related field such as business, engineering, or technical communication. Gaining experience in process documentation, understanding industry standards, and becoming proficient with tools like Microsoft Word or process management software can enhance your qualifications. Building a portfolio of clear, detailed SOPs can help demonstrate your ability to communicate complex procedures effectively.

What are the key skills and qualifications needed to thrive in the SOP writer position, and why are they important?

To thrive as an SOP Writer, you need excellent technical writing skills, strong attention to detail, and an understanding of regulatory or compliance requirements, often supported by a relevant degree such as in English, Technical Communication, or a scientific field. Familiarity with document management systems, process mapping tools, and sometimes quality management software is typically required. Outstanding interpersonal skills, adaptability, and the ability to gather information from diverse subject matter experts help make someone excel in this role. These competencies are crucial for creating clear, accurate, and compliant standard operating procedures that support organizational consistency and efficiency.

What are the typical daily responsibilities of an SOP writer?

As an SOP Writer, your daily responsibilities usually involve working closely with various departments to gather detailed information about processes and translating that information into clear, structured procedure documents. You will review and update existing SOPs, ensure all new documents align with regulatory standards, and coordinate revisions based on stakeholder feedback. Additionally, you'll often participate in process improvement meetings, manage document version control, and may provide guidance or training to employees on following SOPs. This role requires both independent work and regular collaboration to ensure accuracy and compliance in all documentation.

What are the most commonly searched types of Sop Writer jobs in Raleigh, NC? The most popular types of Sop Writer jobs in Raleigh, NC are:
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Sop Writer jobs near you
Infographic showing various Sop Writer job openings in Raleigh, NC as of August 2026, with employment types broken down into 67% Full Time, 11% Part Time, and 22% Contract. Highlights an 100% In-person job distribution, with an average salary of $69,563 per year, or $33.4 per hour.

Sr. Validations Specialist

Alcami Corporation

Morrisville, NC • On-site

$77K - $106K/yr

Full-time

Re-posted 10 hours ago

Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Sr. Validations Specialist is accountable for driving results in a fast-paced environment by supporting general pharmaceutical validation of equipment and GxP computerized systems. Specific responsibilities include reviewing SOP's, composing/revising SOP's and validation master plans; supporting facility, utility, manufacturing equipment, conducting reviews of validation documentation such as validation plans, system/functional requirements, protocols and summary reports; ensuring compliance with 21 CFR Part 11, Data Integrity, and functional requirements; developing documentations as required for projects; serve as the subject matter expert during audits and inspections and consulting on validation and cGMP questions and issues. The ideal candidate will work on extremely complex problems in which analysis of situations or data requires an in-depth evaluation of various factors.
On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:00am - 4:30pm.

Responsibilities
  • Performs the qualification and validation of production equipment, utilities, and computer systems.
  • Assists in equipment selection and specification.
  • Works on complex problems of broad scope in which analysis of situation or data requires a review of identifiable factors.
  • Exercises judgment within defined procedures and practices to determine appropriate action.
  • Maintains all documentation pertaining to qualification and validation.
  • Develops procedures, protocols, and validation project plans.
  • Serves as Validations resource for contractors and vendors.
  • Executes procedures and protocols.
  • Maintain the compliance of validated systems through on-going validation activities (e.g., change control, periodic system reviews, etc.).
  • Composes/revises SOP's and master validation plans.
  • Collaborate with cross-functional teams to assist in the planning, development, installation, operation, validation, and qualification of newly installed or updated equipment and/or computerized systems.
  • Strong knowledge and experience with facility, utility, instrument, and equipment qualifications.
  • Ensures completion & compliance with cGMP and all other relevant company training requirements.
  • Acts as a certified trainer.
  • Provide qualification guidance to IT for infrastructure and computerized system platforms.
  • Other duties as assigned.

Qualifications
  • Bachelor's Degree in Engineering, Chemistry, Biology, or related field required.
  • 5+ years of related experience required.

Knowledge, Skills, and Abilities
  • Excellent knowledge of quality assurance reviews of validations documentation.
  • cGMP training and basic understanding.
  • Excellent knowledge of pharmaceutical GMP environment.
  • Basic knowledge of Kaye AVS.
  • Good understanding of and ability to utilize Pro Cal.
  • Strong communication skills (oral and written).
  • Strong mechanical skills.
  • Strong working knowledge of Microsoft Office applications.
  • Ability to work on multiple projects simultaneously, with strong attention to detail.
  • Ability to train and mentor others.

Travel Expectations
  • Less than 10% travel expected.

Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand; sit and stoop, kneel, crouch, or crawl. The employee is occasionally required to walk. The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
While performing the duties of this Job, the employee is frequently exposed to moving mechanical parts and risk of electrical shock. The employee is occasionally exposed to fumes or airborne particles; toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

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