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"