Technical Writer
About the Site
Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end-to-end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit-for-scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.
About the Role
We have an opportunity for a Technical Writer to join our team. In this role, you will work closely with subject matter experts to create and update essential documentation, ensuring accuracy and compliance. You will support manufacturing and packaging activities by maintaining documentation systems and coordinating approvals. This position offers the chance to contribute to cross-functional projects and play a key role in supporting audits and regulatory requirements.
Shift: Monday - Friday, 8am - 5pm. Location: Greenville, NC. 100% onsite.
Responsibilities
- Collaborate with subject matter experts to gather information for creating or updating documents such as Master Batch Records and protocols, and coordinate related change control documents
- Review documents with subject matter experts and Operations personnel to ensure accuracy, executability, and consistent formatting
- Maintain accuracy of the documentation database and ensure inputs meet company standards
- Assist in making inputs to the Manufacturing Resource Planning system in preparation for manufacturing events
- Close out help desk tickets related to document corrections and updates
- Provide requested information during client and FDA audits
- Participate in cross-functional project development team activities
- Support the continued implementation of electronic document software systems
- Coordinate document approvals across the organization
- Respond quickly and effectively to changing priorities for multiple business units in packaging and manufacturing
Requirements
- Bachelor’s degree in a STEM-related field; OR
- Associate degree in a STEM-related field with at least 2 years of relevant experience; OR
- High school diploma or equivalent with at least 3 years of relevant industry experience
- At least one year of technical writing experience strongly preferred
- Ability to administer quality system programs and resources
- Familiarity with Good Manufacturing Practice documentation requirements
- Proficiency with computer systems such as Microsoft Word, Excel, Adobe Professional, and database management software
- Effective presentation and communication skills, as well as project and resource management skills
Benefits
- Competitive Paid Time Off plus 8 paid holidays
- Medical, dental, and vision benefits effective day one of employment
- Tuition reimbursement to help you complete or earn a new degree
- Engaging site-based activities such as Music Bingo, donation programs, and seasonal events
- Employee Resource Groups promoting diversity and inclusion
- Green initiatives and community engagement programs
- Defined career path with annual performance reviews and growth opportunities
- WellHub program supporting physical and mental wellness, including an onsite fitness center
- Exclusive discounts through Perkspot from over 900 merchants