Technical Writer

Position Summary Work Schedule: Monday-Friday, Days. 100% based on-site in Greenville, NC. Catalent’s Greenville, N.C. facility specializes in end-to-end turn‑key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state‑of‑the‑art facility features fit‑for‑scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. Responsibilities Work with Subject Matter Expert (SME) to gather information needed to create new documents or update existing documents (e.g., Master Batch Records and protocols) and coordinate associated change control documents. Review documents with SME and Operations personnel to ensure they are accurate, executable, and formatting is consistent and harmonized. Ensure the documentation database is accurate and inputs conform to company standards; assist in making inputs to the Manufacturing Resource Planning system in preparation for manufacturing events. Close out help desk tickets regarding document corrections and updates. Provide requested information during client and FDA audits. Participate and contribute to the activities of cross‑functional project development teams and to the continued implementation of electronic document software systems. Coordinate document approval across the organization; provide lean and agile response to changing priorities in service of multiple business units for both packaging and manufacturing activities. Other duties as assigned. The Candidate Requires a Bachelor’s degree in a science‑related field, Engineering, or Industrial Technology, with at least one year of relevant technical writing experience; or Associate degree in a science‑related field, Engineering, or Industrial Technology, with at least two years of relevant technical writing experience; or High school diploma or equivalent with at least three years of relevant technical writing experience. Ability to administer quality system programs and resources. Familiar with GMP documentation requirements. Proficient with Microsoft Office Word and Excel and Adobe Professional. Experience with database management software. Must be able to sit, stand, walk regularly and occasionally lift up to 40 pounds. Benefits Day one benefits: medical, dental, vision, and 401(k) effective on your first day. 152 hours of PTO plus 8 paid holidays. Dynamic, fast‑paced work environment. Opportunity to work on continuous improvement processes. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by emailing View email address on click.appcast.io. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and routed to a local recruiter. #J-18808-Ljbffr