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Manufacturing Technical Writer Jobs in Raleigh, NC

... 7/365 technical assistance for our clients. We provide a comprehensive and certified level of ... Ability to follow written and verbal instructions independently with minimal supervision. * Good ...

... 7/365 technical assistance for our clients. We provide a comprehensive and certified level of ... Ability to follow written and verbal instructions independently with minimal supervision. * Good ...

... 7/365 technical assistance for our clients. We provide a comprehensive and certified level of ... Ability to follow written and verbal instructions independently with minimal supervision. * Good ...

Today our industry leading products are proudly manufactured at facilities throughout the world and ... Conveys technical ideas in written or verbal reports at a suitable level for the audience. * Be a ...

Today our industry leading products are proudly manufactured at facilities throughout the world and ... Conveys technical ideas in written or verbal reports at a suitable level for the audience. * Be a ...

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Manufacturing Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do manufacturing technical writer jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for manufacturing technical writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Manufacturing Technical Writer position, and why are they important?

A Manufacturing Technical Writer should possess strong writing, editing, and document management skills, often supported by a degree in technical communication, engineering, or a related field. Familiarity with authoring tools such as Adobe FrameMaker, MadCap Flare, and knowledge of Document Control Systems (DCS) or Product Lifecycle Management (PLM) are commonly required, along with certifications like CPTC. Excellent communication, attention to detail, and the ability to quickly grasp complex manufacturing processes make candidates stand out. These competencies ensure technical documentation is accurate, clear, and effectively supports safe and efficient manufacturing operations.

What are the typical daily responsibilities of a Manufacturing Technical Writer?

As a Manufacturing Technical Writer, your daily responsibilities typically include researching complex machinery or production processes, creating and updating instruction manuals, standard operating procedures, and safety documentation. You will frequently collaborate with engineers, production managers, and quality assurance teams to gather accurate information and ensure documentation reflects current practices. Reviewing and testing documents for clarity and usability, maintaining version control, and complying with industry or regulatory standards are also central to the role. This position requires a proactive approach to communication and a commitment to continuous improvement in documentation practices.

What is a Manufacturing Technical Writer job?

A Manufacturing Technical Writer creates clear and concise documentation for manufacturing processes, equipment, and standards. They develop user manuals, work instructions, and technical guides to ensure accurate production and compliance. Their role involves collaborating with engineers, operators, and quality teams to translate complex technical details into understandable content. Strong writing, technical expertise, and attention to detail are essential for success in this role.

What are the most commonly searched types of Manufacturing Technical Writer jobs in Raleigh, NC? The most popular types of Manufacturing Technical Writer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Manufacturing Technical Writer jobs? Cities near Raleigh, NC with the most Manufacturing Technical Writer job openings:
Infographic showing various Manufacturing Technical Writer job openings in Raleigh, NC as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $78,739 per year, or $37.9 per hour.

Senior Associate Manufacturing - Continuous Improvement Lead

Amgen, Inc.

Holly Springs, NC โ€ข On-site

Full-time

Posted 5 days ago


Job description

Career Category
Manufacturing
Job Description
Job Description
Join Amgen's Mission of Serving Patients
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Senior Associate Manufacturing - Continuous Improvement Lead
What you will do
Let's do this. Let's change the world. In this vital role you will have the outstanding opportunity to support the start-up of the Amgen North Carolina (ANC) manufacturing facility.
During start up, the Manufacturing Senior Associate Continuous Improvement (CI) Leads will have ownership and oversight of operational readiness activities in manufacturing areas such as: Dispensing, Buffer/Media Preparation, Upstream Cell Culture, Harvest, Downstream Purification, Analytical Testing, or Column Packing. CI leads will support Standard Operating Procedure (SOP) creation, review, and approval; specification and purchasing of required equipment and supplies, design of job aids and work instructions, advancement of digital tools to support manufacturing operations, and training of staff. When the plant transitions to operations in 2025 this position will manage and lead the CI program for MFG.
  • Provide technical support and subject matter expertise for manufacturing area.
  • Oversee support and ongoing development of all the manufacturing systems including SOP, TRNQ, MES, QMS records, among others.
  • Train staff (associates, operators, technical/QA/support) on assigned manufacturing systems.
  • Support troubleshooting needs during commissioning/qualification, start-up, engineering run, and process performance qualification of the ANC manufacturing facility
  • Facilitate process, area, and equipment quality risk assessments as needed to identify risks, failure modes, and mitigating actions.
  • When the plant is in production, manage the CI program; this includes conducting time studies to identify process inefficiencies, leading improvement projects in designated MFG area (i.e. upstream, downstream, solution prep), implementing proper change management, and tracking sustainment of implemented changes.
  • Lead cross-functional CAPAs and EVs as required.
  • Serve as a CI and Human and Organizational Performance champion. Provide training to others on CI and lean principles.
  • Lead learning team meetings and kaizen events.

What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The professional we seek will possess strong project management and innovative thinking as well as these qualifications.
Basic Qualifications:
  • High school diploma / GED and 4 years of Manufacturing or Operations experience OR
  • Associate's degree and 2 years of Manufacturing or Operations experience OR
  • Bachelor's degree and 6 months of Manufacturing or Operations experience
  • Masters degree

Preferred Qualifications:
  • Educational background in Life Sciences, Chemistry, Biochemistry, Industrial Biotechnology, and/or Engineering
  • Strong technical knowledge of drug substance processing (cell culture, harvest, chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing
  • Proficient technical writing and presentation skills so as to communicate complex information effectively with technical and senior management staff
  • Ability to lead small and large cross-functional meetings efficiently.
  • Knowledge of process improvement or lean fundamentals.
  • Collaborate with staff at all levels in the organization, including technical and management staff within manufacturing, process development, engineering, supply chain, and quality

What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Salary Range
92,002.00 USD - 108,605.00 USD