Pharma Technical Writer: SOP & Document Control

Integrated Resources Inc.; Sanford (NC); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in workforce solutions is seeking a Technical Writer in North Carolina. The successful applicant will be responsible for creating and reviewing essential documents while adhering to regulatory standards. Ideal candidates will have extensive experience in technical writing, particularly within the pharmaceutical industry, and must demonstrate superior editing skills and attention to detail. This role emphasizes collaboration with various departments and requires a proven track record in managing documents in compliance with cGMP guidelines.

Qualifications

• At least 5 years of technical writing experience.
• Experience in regulated environments preferred.
• Familiarity with cGMP and safety regulations.

Responsibilities

• Assist in creating and revising documents for the manufacturing department.
• Edit and format incoming document requests and maintain document control.
• Collaborate with departments to ensure content accuracy and compliance.

Skills

Editing

Technical Writing

Document Control

Proofreading

Communication Skills

Education

Bachelor's in Science, Communications, or English

AS in Communications or related field

Job description

A leading company in workforce solutions is seeking a Technical Writer in North Carolina. The successful applicant will be responsible for creating and reviewing essential documents while adhering to regulatory standards. Ideal candidates will have extensive experience in technical writing, particularly within the pharmaceutical industry, and must demonstrate superior editing skills and attention to detail. This role emphasizes collaboration with various departments and requires a proven track record in managing documents in compliance with cGMP guidelines.