Expert Technical Content Creator

3 weeks ago

Shirley, New York, United States Actalent Full time

Key Responsibilities:

  • Review and Enhance Documentation: Adapt and customize 17 existing procedures/SOPs for implementation at the site.
  • Collaborate with Experts: Work closely with the project management team and subject matter experts (SMEs) to ensure accurate information is captured and conveyed.
  • Utilize Documentation Systems: Use Veeva electronic documentation systems for writing, editing, and managing documentation.
  • Maintain Industry Standards: Ensure that all documentation adheres to industry standards and regulatory requirements, including FDA guidelines as applicable.
  • Coordinate with Cross-Functional Teams: Gather information, clarify technical content, and validate procedural accuracy.

Qualifications:

  • Education: Bachelor's degree in English, Technical Communication, Life Sciences, or a related field.
  • Experience: Previous experience in technical writing, preferably within the pharmaceutical or biotechnology industries.
  • Skills: Familiarity with Veeva or similar electronic documentation systems, strong understanding of Good Manufacturing Practice (GMP) and regulatory requirements in pharmaceutical manufacturing.
  • Personal Qualities: Excellent written and verbal communication skills with a strong attention to detail, ability to work independently and collaboratively in a fast-paced environment.

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