Technical Writer – Quality | On-site | West Lebanon, NH
Job Summary:
Novo Nordisk is hiring an experienced Technical Writer to support GMP-compliant documentation, change control, and quality systems at their West Lebanon, NH bioproduction site. This on-site role involves collaboration with subject matter experts (SMEs), training teams, and GMP partners to ensure documentation excellence in a regulated pharmaceutical environment. Ideal for professionals with strong writing, compliance, and technical documentation skills in life sciences or related industries.
Key Responsibilities:
Lead document creation and revision for GMP-compliant standards and operational procedures.
Support change control process and ensure documentation flows through proper approvals (DCCs).
Coach and guide document owners on writing style, format, SOP standards, and technical clarity.
Ensure consistency, readability, and compliance across all local Quality Management System (QMS) documents.
Partner with process teams and SMEs to streamline document processing.
Track metrics and timelines for document lifecycle completion.
Contribute to continuous improvement projects related to document processes and quality systems.
Participate in systematic problem-solving and change management initiatives.
Required Skills & Qualifications:
Education:
Associate’s degree in technical, business, or science-related field required; Bachelor’s degree preferred.
Experience:
5+ years of technical writing experience (life sciences, engineering, or pharma preferred) with an associate degree.
3+ years with a bachelor’s degree preferred.
Technical Skills:
Expertise in MS Word, Adobe Acrobat Pro, Excel, PowerPoint, Visio; HTML knowledge is a plus.
Proven experience with change control systems, GMP documentation, and QMS processes.
Familiarity with LEAN or other process improvement methodologies is a plus.
Soft Skills:
Strong planning, organization, and time management.
Excellent communication and collaboration across cross-functional teams.
Detail-oriented with high standards of quality and compliance.
Perks & Benefits:
Leading compensation with annual performance bonus
36 paid days off (vacation, sick leave, and company holidays)
Health, Dental, and Vision insurance (effective Day 1)
14 weeks Paid Parental Leave
401(k) with guaranteed 8% contribution + match option
Free access to Novo Nordisk pharmaceutical products
Career mentorship and growth opportunities
Company Description:
Novo Nordisk, a global leader in diabetes and rare disease care, operates its West Lebanon site as a manufacturing hub for hemophilia and growth hormone therapies. The site supports end-to-end production and quality processes for global supply, driven by innovation and regulatory excellence.
Work Mode: On-site (Monday to Friday)
Location: West Lebanon, New Hampshire, United States
Salary Range: Not specified – includes competitive pay with annual bonus
Call to Action:
If you're a skilled technical communicator passionate about quality, compliance, and healthcare impact—apply now to join Novo Nordisk and help shape documentation standards in global pharma manufacturing.
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