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Technical Writer

3-5 years
Not Disclosed
10 July 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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.