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Home Based Manufacturing Technical Writer Jobs in Rochester, NH

Scismic Inc

Manufacturing Supervisor

Portsmouth, NH · On-site

$100K - $115K/yr

Strong decision-making, communication, and technical writing skills * Hands-on knowledge of batch records and quality documentation * Familiarity with cleanroom or biologics manufacturing preferred

Scismic Inc

Manufacturing Supervisor

Portsmouth, NH · On-site

$100K - $115K/yr

Strong decision-making, communication, and technical writing skills * Hands-on knowledge of batch records and quality documentation * Familiarity with cleanroom or biologics manufacturing preferred

Lonza

Manufacturing Project Associate

Portsmouth, NH · On-site

This role is based onsite, where working in person supports collaboration and effective execution ... Strong written and verbal communication skills, including technical writing * Ability to manage ...

Lonza

Manufacturing Project Associate

Portsmouth, NH

This role is based onsite, where working in person supports collaboration and effective execution ... Strong written and verbal communication skills, including technical writing * Ability to manage ...

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All JobsHome Based Manufacturing Technical Writer JobsHome Based Manufacturing Technical Writer Jobs in Rochester, NH

Home Based Manufacturing Technical Writer information

See Rochester, NH salary details

$13

$38

$64

How much do home based manufacturing technical writer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for home based manufacturing technical writer in Rochester, NH is $38.11, according to ZipRecruiter salary data. Most workers in this role earn between $28.22 and $46.11 per hour, depending on experience, location, and employer.

How does a Home Based Manufacturing Technical Writer typically collaborate with remote engineering and production teams?

As a Home Based Manufacturing Technical Writer, you’ll frequently communicate with engineers, product managers, and production staff through virtual meetings, email, and collaboration platforms. You’ll review technical documents, clarify complex processes, and request additional information to ensure accuracy in manuals and SOPs. Building strong remote relationships is critical, as you’ll often rely on detailed descriptions, annotated diagrams, and screen-sharing sessions to gather the information needed for clear, compliant documentation.

What are the key skills and qualifications needed to thrive as a Home Based Manufacturing Technical Writer, and why are they important?

To thrive as a Home Based Manufacturing Technical Writer, you need strong technical writing ability, knowledge of manufacturing processes, and often a degree in engineering, technical communication, or a related field. Familiarity with documentation tools like Adobe FrameMaker, Microsoft Word, and content management systems, as well as experience with CAD or product lifecycle management software, is common. Exceptional attention to detail, the ability to explain complex concepts clearly, and strong self-motivation are standout soft skills for this remote role. These skills ensure you can produce accurate, user-friendly documentation that supports safe and efficient manufacturing operations from a home office.

What are Home Based Manufacturing Technical Writers?

Home Based Manufacturing Technical Writers are professionals who create technical documents, manuals, and guides related to manufacturing processes, equipment, and products, all while working remotely from their homes. They translate complex technical information into clear, user-friendly documentation for engineers, production teams, and end users. These writers often collaborate with subject matter experts remotely to ensure accuracy and clarity in their materials. Their work helps improve safety, efficiency, and understanding within manufacturing environments. The flexibility of working from home allows them to serve clients or employers across various regions and industries.
What are the most commonly searched types of Manufacturing Technical Writer jobs in Rochester, NH? The most popular types of Manufacturing Technical Writer jobs in Rochester, NH are:
Home Based Manufacturing Technical Writer jobs near you

MSAT - Process Lead Technical Writer

Lonza

Portsmouth, NH • On-site

Full-time

Posted 5 days ago

Lonza rating

8.2

Company rating: 8.2 out of 10

Based on 41 frontline employees who took The Breakroom Quiz

26th of 71 rated pharmaceutical

Job description

MSAT - Process Lead Technical Writer
Location: On-site, Portsmouth, NH.
The MSAT Process Lead Technical Writer is responsible for the development, revision, and delivery of high-quality manufacturing Batch Records and process documentation that support the production of life-changing therapies. The successful candidate will combine strong technical writing expertise with project management and cross-functional collaboration skills to ensure documentation is accurate, compliant, and delivered on schedule. This position plays a vital role in maintaining operational excellence, regulatory compliance, product quality, and ultimately patient safety.
What you will get:
  • Competitive salary and comprehensive benefits package.
  • Opportunities for career development and advancement.
  • Supportive and collaborative team environment.
  • Access to cutting-edge technology and tools.
  • Commitment to employee well-being and safety.
  • Inclusive workplace culture.
  • Recognition and reward for your contributions.

Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:
  • Authoring of Batch Records, coordination of the delivery of timelines for SOPs and other support documents for approval of batch record, participate in Project Team Meetings to coordinate project schedules and alignment of groups in regards to the writing, review, and approval of process of batch records.
  • Ensure Batch Records are consistently generated and delivered to Manufacturing in a timely manner, to a high level of quality, and with a high level of inter-departmental collaboration that ensures the promotion of Right-First-Time operations on the manufacturing floor.
  • Adhere to established departmental practices and protocols and independently create new cGMP documents. Participates in editing documents and managing document comments. Maintains and reviews schedules.
  • Perform daily work to support technical writing functions, including interacting with internal and external stakeholders/customers, hosting/attending ad hoc meetings and interceding on behalf of the team to resolve obstacles.
  • Support other tasks as required, including Regulatory and Customer Audits, and participation in required reoccurring meetings.
  • Oversee day-to-day activities, including assignment of work, to ensure compliant, timely completion of tasks including support the issuing of batch records, editing and peer reviews as required.

What we are looking for:
  • Bachelor's Degree required, Life Sciences area is preferred.
  • Working experience of pharma/biotech (or equivalent) preferred.
  • 5-10 years in a production environment.
  • Working knowledge of GMP / Biotechnology manufacturing background referred, some experience in QA and/or Documentation creation preferred. Ability to manage multiple priorities.
  • Technical writing in the biotech industry preferred.
  • Project management skills required.
  • Strong MS Word experience required.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life science

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