Technical Writer – LIMS / GMP Documentation (Pharma)

Job Title - OneLIMS EM project technical writer

Location: Swiftwater, PA 18370

Duration: Contractual till Mar 2027 with the possibility of extension

Checklist & relevant keywords:

Experience working with a team on a new digital system to convert information into training materials.

QC (quality control) activities, editing of quality documents (SOP's, guidelines, validation master plans, etc.)

LIMS systems (e.g., LabVantage, iLMS, Sequel, or related systems)

Experience deploying digital systems (e.g., LabWare, LIMS)

pharmaceutical, or biotech environments (e.g., Veeva, GMP)

Description The OneLIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS EM global system for the Swiftwater, PA site. The candidate must perform tasks in an efficient, cGMP compliant, and safe manner. Success...