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Biolinq Incorporated

Senior Technical Documentation Specialist

San Diego, CA, United States

$90,000 to $120,000 USD / year

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Job details

Pay: $90,000 to $120,000 USD / year
Experience: 3+ years of experience in technical documentation, quality systems, manufacturing, engineering support, project coordination, or a related discipline.
Posting language: English
Posted: Nov 6, 2026

Original job description

Description

WARNING about fake job posting scams. There has been a recent wave of scams whereby third parties post fake job openings using a bogus email address that resembles xxxx@biolinq.com. Under the guise of asking you to fill out an application, the scammers are attempting to gather your personal information. See the Federal Trade Commission’s warning on this topic at: https://consumer.ftc.gov/articles/job-scams

The only official source for actual Biolinq job postings/openings is at www.biolinq.com/careers. While other job sites (such as LinkedIn, Indeed or Glassdoor) may pull from Biolinq’s careers web page, you should visit www.biolinq.com/careers to verify the accuracy of the openings found on third party web sites.

About the Company Biolinq is a venture-backed digital health company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes. This dynamic role is a part of a team of engineers and scientists developing a novel intradermal biosensor technology and the associated software data extraction and rendering SDK that will transform the way people manage their metabolic health.

Job Purpose

Biolinq is seeking a highly organized, detail-oriented, and technically proficient Senior Technical Documentation Specialist to support R&D, Operations, Manufacturing, and Quality teams throughout the product development lifecycle.

This role is responsible for developing, revising, coordinating, and driving technical and quality system documentation while ensuring compliance with company procedures and quality requirements. The Technical Document Specialist serves as a key partner to technical teams by converting technical inputs into clear, accurate, and compliant documentation while leveraging AI-enabled tools and automation to improve quality, consistency, and execution speed.

The ideal candidate possesses strong written communication skills, exceptional attention to detail, and the ability to translate technical concepts for diverse stakeholders. This individual thrives in a fast-paced environment, manages multiple priorities simultaneously, and proactively drives documentation activities to completion.

This position is based on-site at Biolinq's headquarters in San Diego, California.

Duties and Responsibilities:

Documentation Development

Develop, revise, and maintain technical, manufacturing, and quality system documentation.
Prepare documentation from technical discussions, design reviews, test data, stakeholder input, and other sources.
Collaborate with subject matter experts to gather information, resolve ambiguities, and ensure documentation accuracy.
Support documents such as manufacturing instructions and records, test documentation, technical reports, change-control records, quality records, and risk-management documentation.

Documentation Quality and Compliance

Ensure compliance with applicable procedures, templates, and quality-system requirements.
Review documentation for accuracy, completeness, consistency, traceability, and clarity.
Verify that documents accurately reflect approved technical content and processes.

Coordination and Execution

Coordinate and drive documentation through review, approval, and release workflows.
Track documentation status and proactively follow up with stakeholders as needed.
Identify and resolve documentation bottlenecks and administrative obstacles.
Partner with cross-functional teams to support timely document review, approval, and release.
Manage multiple documentation activities simultaneously while maintaining quality and responsiveness.

Systems and Process Support

Translate technical information into clear, audience-appropriate documentation.
Effectively leverage AI-enabled tools and automation to research, draft, review, improve, and streamline documentation and related business processes.
Build effective working relationships across functions.
Identify documentation gaps and partner with accountable owners to resolve them.

Key Success Factors

Success in this role is measured by:

High-quality, compliant documentation with minimal review findings or rework.
Timely completion of review, approval, and release activities.
Effective coordination across multiple assignments and stakeholder groups.
Ability to independently gather information and drive activities to completion.
Effective application of AI-enabled tools and emerging technologies to improve documentation quality, consistency, efficiency, and stakeholder productivity.

Requirements

Qualifications

Bachelor's degree or equivalent professional experience.
3+ years of experience in technical documentation, quality systems, manufacturing, engineering support, project coordination, or a related discipline.
Outstanding written, verbal, and interpersonal communication skills.
Exceptional attention to detail and organizational skills.
Advanced proficiency with AI-enabled productivity tools and a demonstrated ability to apply them effectively to technical documentation, process improvement, and workflow automation.
Proven ability to manage multiple concurrent projects and priorities.
Strong analytical and problem-solving abilities.
Ability to quickly learn technical concepts and processes.
Proficiency with Microsoft Office applications and document management systems.

Preferred:

Experience within a medical device, biotechnology, pharmaceutical, aerospace, or other highly regulated industry.
Experience supporting product development teams (e.g., engineering, manufacturing, quality, regulatory, etc.)
Demonstrated ability to adopt new technologies and drive process improvements in a fast-paced product development environment.
Familiarity with Quality Management Systems and design control requirements.
Experience with eQMS and document control systems.
Experience with manufacturing, quality, test, documentation (e.g., DHRs, MPIs, BRs, NCMRs, and COs).
Familiarity with FDA Quality System Regulation, ISO 13485, and related quality frameworks.

Working Conditions

Primarily based on-site, in an office and laboratory environment
Occasional travel (up to 10%) may be required to development activities

Physical Requirements

While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands and fingers; manipulate office equipment, including a personal computer; handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office and/or manufacturing environment. Employee may occasionally lift/or move up to 50 pounds.

BENEFITS

Medical, dental, vision, health savings account, flexible spending account, life and long-term disability insurance, 401(k) plan, holidays, and PTO.

At Biolinq we fully subscribe to the principles of Equal Employment Opportunity. It is our policy to provide employment, compensation, and other benefits related to employment based on qualifications, without regard to race, color, religion, national origin, age, sex, veteran status, genetic information, disability, or any other basis prohibited by federal, state or local law. In accordance with requirements of the Americans with Disabilities Act and applicable federal, state and/or local laws, it is our policy to provide reasonable accommodation upon request during the application process to applicants in order that they may be given a full and fair opportunity to be considered for employment. As an Equal

Opportunity Employer, we intend to comply fully with applicable federal, state and/or local employment laws and the information requested on this application will only be used for purposes consistent with those laws. To the extent required by applicable law, The Company maintains a smoke- free workplace.

As part of our efforts to ensure fair and equal pay based on merit, Biolinq supports pay transparency internally and during the recruitment process. The U.S. base salary range reasonably expected to be paid for this role is: $90,000 to $120,000 per year. We may ultimately pay more or less than the posted range. Actual compensation packages are commensurate with experience and based on a variety of factors that are unique to each candidate including, but not limited to: skill set, depth of experience, education, certifications, and specific work location. The range displayed reflects the minimum and maximum target for new hire salaries for the job across the U.S. The total compensation package for this position may also include an annual performance bonus and/or other applicable incentive compensation plans. Biolinq also offers a comprehensive package of benefits including paid time off (vacation, holidays, sick time, parental leave), medical/dental/vision insurance, and 401(k) to eligible employees, subject to the terms and conditions of the applicable plans and any written agreement between the parties. Your recruiter can share more about the total compensation package during the hiring process.

Please note: The information contained herein is not intended to be an all-inclusive list of duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Biolinq Talent Acquisition at Careers@biolinq.com

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