Inteldot has over 11 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.

Description:

Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, checklists, guide, and related technical and business process documentation.

Responsibilities:

  • Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, checklists, guide, and related technical and business process documentation.
  • When creating, updating and enhancing the documentation, adhere to format, content and style guidelines, giving consideration to usability and ensuring accuracy, consistency and quality.
  • Administer the processing of documents via the established Document Processing Review process.
  • May require communication through a variety of media (e.g., CD, intranet, on-line training, etc.).


Competencies / Skills:

  • Previous experience in GMP environment Practical Knowledge revision document such as SOP.
  • Basic knowledge in Electronic system such as Veeva for document revision.
  • Basic knowledge in Project Management (need to know how to manage multiple document in different workflow at the same time).
  • MS Office expertise; previous technical writing experience; regulated environment experience; document version control experience.

Education:

Doctorate degree or Master’s degree and 3 years of experience; or Bachelor’s degree and 5 years of experience.

Compensation and Benefits:

  • Employment (W2) and Professional Services Contract (480) available.
  • Administrative, per project needs. Support during extended hours including weekends, as per business needs, in a flex commuter work setting with the flexibility to be onsite if it is needed.
  • Competitive Pay Rate