Technical Writer

Actalent Inc

Minneapolis, MN(remote)

JOB DETAILS
SALARY
SKILLS
Artificial Intelligence (AI), Biology, Candidate Screening, Communication Skills, Continuous Improvement, Cross-Functional, Design Services, Design Verification, Detail Oriented, Document Management, Documentation, Documentation Format, Documentation Review, Documentation Standards, English Language, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Genetics, Healthcare, ISO (International Organization for Standardization), Manufacturing, Medical Equipment, Medical Products, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Multitasking, Organizational Skills, Presentation/Verbal Skills, Product Development, Product Documentation, Product Packaging, Product Support, Product Testing, Project/Program Management, Proofreading, Quality Assurance Methodology, Regulations, Technical Editing, Technical Support, Technical Writing, Technical/Engineering Design, Test Data, Testing, Validation Documentation, Validation Testing, Work From Home, Writing Skills
LOCATION
Minneapolis, MN
POSTED
2 days ago

Job Title: Technical Writer

This Technical Writer role supports design verification, packaging validation, and product testing activities for medical device development programs. You will create, revise, and maintain technical documentation that underpins product development and verification efforts, ensuring all materials are accurate, compliant, traceable, and audit-ready. The position is ideal for a detail-oriented professional with experience developing technical documentation in a regulated environment, particularly within medical device product development, design verification, validation, packaging, and testing.

Responsibilities

  • Develop, edit, format, and maintain technical documents that support design verification and product testing activities.
  • Collaborate closely with engineering, quality, regulatory, packaging, and test teams to gather technical information and accurately document results.
  • Create and update protocols, reports, test methods, work instructions, procedures, technical summaries, and other supporting documentation.
  • Review engineering and testing data to ensure accuracy, completeness, and consistency within packaging validation and verification documentation.
  • Ensure all documentation complies with applicable quality system requirements and established document control processes.
  • Maintain document traceability and revision history in accordance with internal procedures and standards.
  • Participate in document reviews and incorporate feedback from stakeholders to improve clarity and compliance.
  • Support audit and regulatory readiness by ensuring documentation sets are complete, organized, and compliant.
  • Assist with continuous improvement initiatives focused on enhancing technical documentation processes and standards.

Essential Skills

  • Minimum of 2 years of professional technical writing experience.
  • Experience creating technical documentation in an engineering, manufacturing, life sciences, healthcare, or other regulated environment.
  • Strong technical writing, editing, proofreading, and document formatting skills.
  • Ability to interpret engineering, testing, and technical information and translate it into clear, concise documentation.
  • Experience working cross-functionally with engineers and technical subject matter experts.
  • Proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint.
  • Strong attention to detail and excellent organizational skills.
  • Excellent verbal and written communication skills.
  • Ability to manage multiple projects and priorities effectively in a remote work environment.

Additional Skills & Qualifications

  • Experience within the medical device industry is strongly preferred.
  • Knowledge of design control, design verification, validation, and product development documentation.
  • Experience supporting packaging validation and testing activities.
  • Familiarity with FDA, ISO, GMP, or other regulated quality systems and standards.
  • Experience working with document management systems and controlled documentation processes.
  • Bachelor"s degree in Technical Communication, Engineering, Life Sciences, English, or a related field.
  • Motivation to support critical product development and verification activities within a highly regulated environment.

Work Environment

This role operates within standard business hours of 8:00 AM to 5:00 PM EST and is structured for a remote work environment, requiring effective self-management and virtual collaboration. No travel is expected. You will work in a professional setting focused on highly regulated product development, leveraging common office technologies such as Microsoft Office and document management systems to create and maintain controlled documentation.

Job Type & Location

This is a Contract position based out of Minneapolis, MN.

Pay and Benefits

The pay range for this position is $48.00 - $48.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Jul 31, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

About the Company

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Actalent Inc