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Director Biotech Technical Writer Jobs (NOW HIRING)

The ideal candidate will be a critical thinker with experience in biotechnology or pharmaceuticals, excellent writing skills, and ready to apply specialized skills in technical writing, compliance ...

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Technical Writer - Manufacturing Sciences Location: Carlsbad, CA Pay Rate: $33.00 per hour Position ... Experience working in a pharmaceutical, biotechnology, medical device, or other regulated ...

Technical Writer Location: Santa Clara, CA Customer: J&J JD: Key Responsibilities * Bachelor ... com Direct: 4705239688 Led by 25+ Years of Industry Experience E-Verify ® is a registered ...

Company Description Direct Client Title: Technical Writer Location: Columbia, SC Duration: 12 months Description: SCOPE OF THE PROJECT: Client, as the state Medicaid Agency, is required to develop ...

Direct Hire Whats in it for you: Direct Opportunity Benefits offered through client Opportunity to shine at an awesome company See below and apply now! The Technical Writer is responsible for ...

Technical Writer

Hackensack, NJ · On-site

$48K - $58K/hr

Additionally, the Technical Writer will collaborate closely with the Compliance Director to update and enhance compliance documents as necessary. Responsibilities: * Develop comprehensive department ...

Technical Writer

Minneapolis, MN · On-site

$75K - $100K/yr

Technical Writer - Industrial Equipment Brooklyn Park, MN | Direct Hire | $75,000-$100,000 Konik is partnering with an innovative manufacturer of advanced laser-processing equipment to add a ...

Technical Writer direct client Duration: 6 Months Location: Pittsburgh, PA or Irving, TX Immediate Interview Job responsibilities: Assists in researching, writing, editing, and proofreading technical ...

TECHNICAL WRITER

Hollywood, MD · On-site

$66K - $86K/yr

Director of Quality Assurance CLASSIFICATION: Exempt Primary Function The Technical Writer plays a critical role in ensuring clear, accurate, and concise documentation across multiple departments ...

$66K - $86K/yr

Director of Quality Assurance CLASSIFICATION: Exempt Primary Function The Technical Writer plays a critical role in ensuring clear, accurate, and concise documentation across multiple departments ...

GMP Technical Writer

Madison, WI · On-site

$50 - $70/hr

Requirements Required Qualifications & Experience * 4+ years of GMP technical writing experiencewithin pharmaceutical, biotechnology, medical device, or other regulatedmanufacturing environments.

... directed style guides • Ability to work with technical cyber analysts to evaluate material and ... years technical writing and editing experience with a high school diploma Preferred : • ...

Establish and maintain files and documentation, both hard copy (when directed by the COR) and ... of technical writing tasks, including presentations and reports * Ability to support high ...

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Director Biotech Technical Writer information

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How much do director biotech technical writer jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for director biotech technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

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QA Technical Writer

Memphis, TN • On-site

RADgov Inc.
IT Services • 51 - 200 employees

Other

Posted 2 days ago

New


Job description

Reporting to the Manager Compliance, the Compliance Specialist is responsible for creating, managing, and maintaining technical documentation for our cell and gene therapy manufacturing site. This includes writing, editing, and reviewing documents such as quality systems (deviations, change controls and capas). The ideal candidate will be a critical thinker with experience in biotechnology or pharmaceuticals, excellent writing skills, and ready to apply specialized skills in technical writing, compliance, data analysis…etc..in a regulated environment.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Generate and leading the facilitation in the completion of quality system documents for the manufacturing site (Deviations, CAPAs, Change Controls, etc)
  • Ensure all documentation is clear, concise, and adheres to company standards and regulatory guidelines
  • Complete routine and some non-routine documentation assignments within prescribed timeline under general supervision
  • Work closely with stakeholders to gather information and ensure accuracy and completeness of documentation
  • Facilitate document reviews and approvals, incorporating feedback from cross-functional teams and clients
  • Collaborate in writing and editing technical documents including standard operating procedures (SOPs), batch records, technical reports, etc
  • Communicate results and/or concerns verbally and in writing
  • Develop and maintain relationships with internal stakeholders as well as begin building relationships with clients
  • Provides solutions of moderate to complex scope to continuously improve documentation processes and templates to enhance clarity, efficiency, and compliance
  • Leads in performing trainings for internal team and functional departments as applicable
  • Perform other duties as assigned
EDUCATION AND/OR WORK EXPERIENCE REQUIREMENTS:
  • Associate’s degree or higher in Life Sciences, Biotechnology, Biochemistry, or related field preferred
  • Minimum of 2-6 years of technical writing experience in the biotechnology or pharmaceutical industry, preferably in cell and gene therapy
  • Exceptional writing, editing, and proofreading skills with attention to detail
  • Ability to interpret and present complex scientific data in a clear and concise manner
  • Proficient in Microsoft Office Suite and document management systems
  • Strong organizational and project management skills
  • Excellent communication and interpersonal skills
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