Senior QC Technical Writer & Doc Process Lead

Novo Nordisk A/S

Clayton, Northern (NC, KY)

Hybrid

USD 85,000 - 115,000

Full time

6 days ago

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Benefits offered by this job

Leading pay & annual bonus

14 paid holidays

Health, Dental, Vision insurance (day

401K with company match

Job summary

Novo Nordisk in Clayton, NC is seeking a Senior Technical Writer to design, improve, and maintain the document creation and revision process for QC documents at site Clayton. You will serve as the English language technical writing expert for QC documents and lead, train, and mentor other QC technical writers and SMEs.

You will collaborate with Process Responsible personnel on-site and report to the Manager, QC Support.

Qualifications

Bachelor's degree or equivalent in a relevant field.
Minimum five years of technical writing experience, preferably in engineering, life sciences, software, or related fields.
Ability to read, write and understand complex product documentation and SOPs with high-level concepts.
Knowledge of GMP concepts and process improvement methodologies (LEAN preferred).
Experience with change management and cross-functional collaboration.

Responsibilities

Design and own the process for implementing new QC documents (API, IFP, OFP) and the related change control.
Improve local change process for QC document revisions for ease of use by owners, users and approvers.
Collaborate cross-functionally and maintain stakeholder relationships.
Support authors with language usage, document control processes and tools.
Review local QC documents for clarity and reader-friendliness language.
Participate in SOP Expert Network, Process Workshops, and document governance groups.