Medical Technical Writer, Elizabeth

Roles & Responsibilities:

3+ years of experience in the Pharma and/or Consumer Health industry.

Strong understanding of regulatory requirements and industry standards.

Previous experience in Document Management systems (e.g., Veeva, Documentum, Enovia) to create, store, and manage documents is preferred.

Previous experience with Document Management, GxP Records and Learning Management (Training Management) processes in regulated business is preferred.

3+ years of experience in technical writing, with a focus on procedure development and revision.

Proven ability to write clear, concise, and accurate technical documents.

Strong knowledge of Microsoft Office Suite (Word, Excel, PowerPoint).

High proficiency in English, both written and verbal.

Excellent communication and interpersonal skills.

Structured and well-organized Strong attention to detail and ability to manage multiple projects simultaneously.

Ability to work independently and as part of a team.