Job Title: Technical Writer - II
Location: Andover, MA 01810
Duration: 12 Months (Possibility of extension depending upon business requirements and performance)

 
Job Summary:

• This role will provide non-testing support to the QC Product Technical Support department.
• This scope includes coordination of generating validation documents to support product validation at the client Andover site.
• The technical skills within scope will require understanding of the scientific principles of test methods, data analysis and cGMP requirement.
• The candidate will be responsible for facilitating lifecycle management through collaboration with laboratory subject matter experts (SMEs) and analysts at organization.

 
The key responsibilities of the candidate are as follows:

• Authoring method validation documents using organization document workflow, through collaboration with SMEs Use of the Laboratory Management System (LIMS) Supporting assay improvement activities and generating supporting documents.
• Participating in across site meetings and tracking the project timeline.

 
Successful candidate requires:

• Knowledge of QC microbial support and technical writing Strong interpersonal and written communication skills.
• A detail-oriented approach to deliverables as the main job responsibility is data review and generation of GMP documentation.
• A degree in science, preferably in microbiology or related technical discipline.
• Past experience supporting GMP writing in the biopharmaceutical field.

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 50.00/hr.