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Evening Manufacturing Technical Writer Jobs in Rochester, NH

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

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

Manufacturing Project Associate Location: Portsmouth, NH, (On-site) As a Manufacturing Project ... Strong written and verbal communication skills, including technical writing * Ability to manage ...

Job Title: Manufacturing Associate III Location: Portsmouth, NH, (On-site) As a Manufacturing ... Strong communication skills, including technical writing * Attention to detail with strong problem ...

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Manufacturing Engineer

Dover, NH · On-site

$74K - $96K/yr

Provide technical support and training to manufacturing staff and operators. * Manage projects ... Qualifications * Strong written and verbal communication skills; able to create and deliver ...

Manufacturing Engineer

Dover, NH · On-site

$74K - $96K/yr

Provide technical support and training to manufacturing staff and operators. * Manage projects ... Qualifications * Strong written and verbal communication skills; able to create and deliver ...

Manufacturing Engineer

Dover, NH · On-site

$74K - $96K/yr

Provide technical support and training to manufacturing staff and operators. * Manage projects ... Qualifications * Strong written and verbal communication skills; able to create and deliver ...

Manufacturing Engineer I

Portsmouth, NH · On-site

$74K - $95K/yr

Manufacturing Engineers are a core component of the engineering team, serving as the technical ... Strong verbal and written communication skills. * Proficient in the use of SolidWorks to design ...

Manufacturing Engineer I

Newington, NH · On-site

$74K - $95K/yr

Manufacturing Engineers are a core component of the engineering team, serving as the technical ... Strong verbal and written communication skills. * Proficient in the use of SolidWorks to design ...

Manufacturing Engineer III

Exeter, NH · On-site

$74K - $95K/yr

You'll also find real opportunities to learn, grow, and advance, whether you're building technical ... Writing justification for capital projects * New equipment implementation/validation (IQ, OQ, PQ)

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Evening Manufacturing Technical Writer information

See Rochester, NH salary details

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How much do evening manufacturing technical writer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for evening 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.

What does an Evening Manufacturing Technical Writer do?

An Evening Manufacturing Technical Writer creates and updates technical documents, such as manuals, work instructions, and process guides, specifically for manufacturing operations that occur during evening shifts. They collaborate with engineers, production staff, and quality teams to ensure documentation is accurate, clear, and compliant with industry standards. Their work helps support smooth shift transitions, consistent training, and regulatory compliance in a manufacturing environment. The evening schedule enables them to provide real-time support and capture details unique to the evening shift.

What are some common challenges faced by Evening Manufacturing Technical Writers, and how can they be addressed?

Evening Manufacturing Technical Writers often face challenges such as limited access to subject matter experts during off-hours and tight production deadlines. To overcome these, it's helpful to proactively schedule interviews or gather necessary information from day-shift staff ahead of time and make use of detailed process documentation. Additionally, effective communication with cross-functional teams and maintaining organized notes can help ensure accuracy and efficiency when developing technical documents.

What are the key skills and qualifications needed to thrive as an Evening Manufacturing Technical Writer, and why are they important?

To thrive as an Evening Manufacturing Technical Writer, you need strong writing, editing, and document management skills, often backed by a degree in English, technical communication, or engineering. Familiarity with document control systems, content management software, and manufacturing-specific standards (like ISO or GMP) is typically required. Excellent attention to detail, time management, and the ability to communicate complex information clearly are crucial soft skills for this role. These abilities ensure accurate and effective technical documentation that supports manufacturing processes, compliance, and operational efficiency during evening shifts.
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:

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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