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Catalent

Global contract drug formulation, manufacturing, packaging

Technical Writer

Technical WritingConfirmed live in the last 24 hours
Full-timeGreenville, NC, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a STEM-related field and at least 1 year of relevant experience, or an associate degree in a STEM-related field and at least 2 years of relevant experience, or a high school diploma or equivalent and at least 3 years of relevant industry experience.
  • Ability to administer quality system programs and resources.
  • Familiarity with Good Manufacturing Practice (GMP) documentation requirements.
  • Proficiency with Microsoft Office Word, Excel, Adobe Professional, and database management software.
  • Ability to occasionally lift 40 pounds unassisted and occasionally push and pull a maximum of 100 pounds.
  • Ability to perform work involving sitting, standing, walking, simple grasping, fine manipulation, climbing, bending, stooping, twisting, and full range of motion in the upper and lower extremities.
  • Occasional exposure to dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid, and wet environments.

Responsibilities

  • Collect, organize, format, and author documents, and make inputs into the site inventory management system for manufacturing activities.
  • Work with subject matter experts to gather information for new or updated documents, including Master Batch Records and protocols, and coordinate associated change control documents.
  • Review documents with subject matter experts and Operations personnel to ensure accuracy, executability, consistent formatting, and harmonization.
  • Ensure the documentation database is accurate and its inputs conform to company standards.
  • Make or assist with inputs to Manufacturing Resource Planning 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 cross-functional project development teams.
  • Participate and contribute to continued implementation of electronic document software systems.
  • Coordinate document approval across the organization.
  • Respond to changing priorities across multiple business units for packaging and manufacturing activities.
  • Perform other duties as assigned.

Desired Qualifications

  • At least one year of technical writing experience is strongly preferred.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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