Technical Writer
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports ...
San Jose, CA · On-site
... manufacturing teams and internal product management to capture the essential ideas, intent, stated ... Technical Writer/project manager: 5 - 8 years of experience in creating, writing, editing and ...
San Jose, CA · On-site
... manufacturing teams and internal product management to capture the essential ideas, intent, stated ... Technical Writer/project manager: 5 - 8 years of experience in creating, writing, editing and ...
Be Seen First
San Diego, CA · On-site
$55 - $75/hr
We have an opening for a Principal Technical Editor / Writer to join our team of qualified ... manufacturing. To learn more, please visit www.acrocorp.com.
New
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Be Seen First
San Diego, CA · On-site
$55 - $75/hr
We have an opening for a Principal Technical Editor / Writer to join our team of qualified ... manufacturing. To learn more, please visit www.acrocorp.com.
New
Morgan Hill, CA · On-site
$85K - $130K/hr
... solutions for R&D, manufacturing, installation, and maintenance applications, as well as ... As a Technical Writer based in Morgan Hill, CA, you will have responsibility for creating and ...
Morgan Hill, CA · On-site
$85K - $130K/hr
... solutions for R&D, manufacturing, installation, and maintenance applications, as well as ... As a Technical Writer based in Morgan Hill, CA, you will have responsibility for creating and ...
Irvine, CA · On-site
$85K - $110K/yr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85K - $110K/yr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85K - $110K/yr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85K - $110K/yr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85 - $110/hr
Collaborate with a team to create technical documentation, specification writing, technical ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85 - $110/hr
Collaborate with a team to create technical documentation, specification writing, technical ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Morgan Hill, CA · On-site
$85K - $130K/yr
... solutions for R&D, manufacturing, installation, and maintenance applications, as well as ... As a Technical Writer based in Morgan Hill, CA, you will have responsibility for creating and ...
Morgan Hill, CA · On-site
$85K - $130K/yr
... solutions for R&D, manufacturing, installation, and maintenance applications, as well as ... As a Technical Writer based in Morgan Hill, CA, you will have responsibility for creating and ...
Irvine, CA · On-site
$85 - $110/hr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85 - $110/hr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
CA · On-site
$36 - $41/hr
We are currently looking for a Contract Technical Writer to work for a leading Greater Orange County area contract development and manufacturing organization. Pay Rate: $36-41+/hr ($75-85k) depending ...
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CA · On-site
$36 - $41/hr
We are currently looking for a Contract Technical Writer to work for a leading Greater Orange County area contract development and manufacturing organization. Pay Rate: $36-41+/hr ($75-85k) depending ...
Irvine, CA · On-site
$85 - $110/hr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Irvine, CA · On-site
$85 - $110/hr
Keep technical documentation on projects according to ISO 9001/13485 quality management system ... Manufacturing Instruction Writing * Familiarity with equipment testing (Verification & Validation ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ...
Must have Pharma/Manufacturing Tech Writing experience. * Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and Quality Systems, with the ability to assess ...
Must have Pharma/Manufacturing Tech Writing experience. * Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and Quality Systems, with the ability to assess ...
You will work closely with senior writers, engineers, technical program managers, manufacturing team members, and other stakeholders to ensure that documentation complies with industry standards and ...
You will work closely with senior writers, engineers, technical program managers, manufacturing team members, and other stakeholders to ensure that documentation complies with industry standards and ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. * Demonstrates ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. * Demonstrates ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ...
Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and ... Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ...
Port Hueneme, CA · On-site
$70 - $90/hr
They access technical data such as drawings, specifications, parts lists, and manufacturer ... Ability to write, revise, and organize technical material for manuals, procedures, reports, and ...
Port Hueneme, CA · On-site
$70 - $90/hr
They access technical data such as drawings, specifications, parts lists, and manufacturer ... Ability to write, revise, and organize technical material for manuals, procedures, reports, and ...
They access technical data such as drawings, specifications, parts lists, and manufacturer ... Ability to write, revise, and organize technical material for manuals, procedures, reports, and ...
They access technical data such as drawings, specifications, parts lists, and manufacturer ... Ability to write, revise, and organize technical material for manuals, procedures, reports, and ...
Sacramento, CA · On-site
... or manufacturing similar organizations. * Experience mapping and analyzing complex business ... Technical writing projects experience Developing detailed business process documentation and ...
Quick apply
Sacramento, CA · On-site
... or manufacturing similar organizations. * Experience mapping and analyzing complex business ... Technical writing projects experience Developing detailed business process documentation and ...
San Luis Obispo, CA · On-site
$80K - $97K/yr
You will work closely with senior writers, engineers, technical program managers, manufacturing team members, and other stakeholders to ensure that documentation complies with industry standards and ...
San Luis Obispo, CA · On-site
$80K - $97K/yr
You will work closely with senior writers, engineers, technical program managers, manufacturing team members, and other stakeholders to ensure that documentation complies with industry standards and ...
$13.52 - $18.22
2% of jobs
$18.22 - $22.93
7% of jobs
$22.93 - $27.63
12% of jobs
$28.72 is the 25th percentile. Wages below this are outliers.
$27.63 - $32.33
16% of jobs
The median wage is $35.86 / hr.
$32.33 - $37.03
17% of jobs
$37.03 - $41.73
14% of jobs
$44.79 is the 75th percentile. Wages above this are outliers.
$41.73 - $46.43
11% of jobs
$46.43 - $51.14
10% of jobs
$51.14 - $55.84
5% of jobs
$55.84 - $60.54
3% of jobs
$60.54 - $65.24
3% of jobs
$13
$38
$65
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.
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.
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.
The most popular types of Manufacturing Technical Writer jobs in California are:
For Manufacturing Technical Writer jobs in California, the most frequently searched job titles are:
The top searched job categories for Manufacturing Technical Writer jobs in California are:
Cities in California with the most Manufacturing Technical Writer job openings:

$68K - $96K/yr
Full-time
Re-posted 4 days ago
8.2
Based on 31 frontline employees who took The Breakroom Quiz
86th of 545 rated manufacturers
Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team, part of the AI, Product and Platforms organization, is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It is our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
At Edwards Lifesciences, the IHFM AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated software traceable and audit ready. You produce and maintain design control artifacts and user-facing documentation with limited guidance, partnering with engineering, quality, and product.
Based in Irvine, CA, you'll join a high-impact medtech innovation hub in the heart of Orange County, collaborating in person with cross-functional teams to shape patient-focused technology.
How You'll Make an ImpactCreate and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports, technical summaries, and test procedures.
Develop well-scoped controlled documentation that supports regulated software traceability and audit readiness.
Maintain documentation in a standard format and follow established guidelines for content quality, organization, and consistency.
Partner with production employees, technicians, engineers, project teams, regulatory partners, and management to understand product, component, or device changes.
Review documents for style, clarity, grammar, punctuation, and overall usability.
Identify and resolve inconsistencies in content, structure, or document development, and work with authors to recommend appropriate updates.
Respond to requests for clarification or explanation of reference materials and technical documentation.
Support additional documentation-related needs as assigned by leadership.
Bachelor's degree in a related field and 3 years of technical writing experience, or equivalent work experience based on Edwards criteria.
This is an onsite role based in Irvine, CA. Relocation assistance is not provided, and candidates must reside within a 50-mile radius of Irvine to be considered.
Biotechnology, medical device, or regulated industry experience, or equivalent work experience based on Edwards criteria.
Experience creating or maintaining documentation types such as procedures, routers, process sheets, technical summaries, protocols, and test reports.
Solid understanding of policies, procedures, and guidelines relevant to technical documentation development.
Strong editing, proofreading, and technical writing skills, with careful attention to style, clarity, grammar, and punctuation.
Proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, and Publisher; Adobe and Photoshop experience preferred.
Good written and verbal communication skills in English, with strong interpersonal skills.
Good problem-solving, critical thinking, organization, and prioritization skills in a fast-paced environment.
Ability to work independently on more complex projects or lines of work, with work reviewed for accuracy and soundness.
Ability to collaborate across interdepartmental teams, build productive internal and external working relationships, and represent the organization on specific projects.
Strict attention to detail and commitment to following all company rules and requirements, including Environmental Health & Safety expectations and applicable protocols.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $68,000 to $96,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
Get the full story on Breakroom
Sourced by ZipRecruiter
Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.
Medical equipment and supplies manufacturing
10,000+ Employees
Irvine, CA, US
1958