Specialist Technical Writing (Smartsheet, GMP, GDP, SOP) Pharma/Biotech

Aequor; Holly Springs (NC); On-site; USD 65,000 - 85,000; Full time

Job summary

A pharmaceutical company based in Holly Springs, NC, is seeking a Specialist Technical Writer with expertise in GMP, cGMP, GDP, and Smartsheet. The ideal candidate will have over 2 years of relevant experience in the Pharma/BioPharma/Biotech industry and strong skills in MS Word. Responsibilities include developing, writing, and editing various technical documents such as SOPs and manuals. This is a hybrid role offering a contract position with a mid-senior level title.

Qualifications

• 2+ years of relevant experience in technical writing.
• Experience in the pharmaceutical industry is a plus.

Responsibilities

• Develops, writes, edits, and formats materials such as SOPs, business practices, forms, and manuals.

Skills

GMP experience

cGMP experience

GDP experience

Smartsheet experience

Strong MS Word program experience

Pharma/BioPharma/Biotech industry experience

Education

Bachelor of Science

Job description

Specialist Technical Writing (Smartsheet, GMP, GDP, SOP) Pharma/Biotech

Direct message the job poster from Aequor.

Role: Specialist Technical Writing

Location: Holly Springs, NC (Hybrid)

• Bachelor of Science with 2+ years of relevant experience.
• GMP, cGMP, GDP and Smartsheet experience.
• Strong MS Word program experience.
• Pharma/BioPharma/Biotech industry experience.

Responsibilities:

• Develops, writes, edits, and formats materials such as Standard Operating Procedures (SOPs), business practices, forms, checklists, technical manuals, installation guides, user manuals, and related technical and business process documentation.

Seniority Level: Mid-Senior level

Employment Type: Contract

Job Function: Writing/Editing, Art/Creative, and Advertising

Industries: Pharmaceutical Manufacturing, Chemical Manufacturing, and Chemical Raw Materials Manufacturing