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Associate Technical Writing

Holly Springs, NC
Description:
Note:
  • Fully Onsite in Holly Springs, NC - Schedule will be determined once site is operational. Possible weekend shifts. Likely Monday - Friday working 8-5. Rare opportunity for overtime.

Job Details: 
  • Develops, writes, edits, and formats materials such as Standard Operating Procedures, forms, methods and related technical and business process documentation for the Quality Control organization.
  • When creating, updating and enhancing the documentation, adhere to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality.
  • Additionally, this position will be required to administer the processing of documents in the controlled document system.

Skills:
  • MS Office expertise
  • Technical writing experience
  • Excellent communication/writing skills
  • Knowledge of Good Documentation Practices preferred
  • General laboratory/quality control knowledge preferred

Basic Qualifications
  • Associate Quality Assurance

Top 3 Must Have Skill Sets:       
  • Technical writing experience required.
  • Strong attention to detail and the ability to self manage work/projects
  • 1+ year of previous pharma experience with a understanding of the GMP process.

Day to Day Responsibilities:
  • Assist with writing laboratory documentation (standard operating procedures, guidance documents, forms, etc) for the QC Laboratory group. Manage the review/approval process in the controlled document system.
  • Assist other lab staff with formatting/editing of documents. Update/help manage master document tracker for new lab startup project.

PAY RATE : $30/Hr on W2.

"This posting is for Contingent Worker, not an FTE"

 

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