Blackfield Associates are supporting a Global pharmaceutical manufacturer in their search for a Technical Writer to join their project based in North Carolina on an initial 12-month contract.
Key Responsibilities:
- Assist document owners with drafting, revising, and managing the change control process.
- Write and handle deviations, ensuring proper documentation management and clarity in local QMS documents.
- Convert production tasks into job instructions (JIs) and troubleshoot iDoc-related issues.
- Collaborate with Learning & Development, Quality, and other cross-functional teams.
- Offer expertise in document structure, style, and language usage to improve operational documents.
- Support standardization projects and assist with revisions of IFP Framework level documents.
- Build and maintain relationships with internal and external stakeholders to ensure project deadlines and metrics are met.
Required Skills/Qualifications:
- Associate’s degree in a technical field or equivalent experience, with sufficient experience in technical writing.
- Proficient in MS Word, Adobe Acrobat, Excel, PowerPoint, Visio, and experienced with change control.
- Familiarity with GMP concepts and process improvement methodologies like LEAN is preferred.
- Strong organizational skills and expertise in managing multiple change requests (CRs).
- Preferred experience in engineering, life sciences, or software industries.