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Tech Digital Group

Technical Writer

Bothell, WA · On-site

Technical Writer Schedule: M-F, Normal business hours, 100% Onsite Top Skills: • Bachelor's degree in a relevant scientific field (e.g., Biology, Chemistry, Life Sciences) or equivalent combination ...

Air Methods

Technical Writer

Englewood, CO · On-site

$80K/yr

Provide quoted hours for assigned work tasks * Other duties as assigned. Additional Job ... Experience with CAD software (SolidWorks and AutoCAD preferred) and data vault and management ...

CultureFit

Technical Writer

Chicago, IL

A. in English, Creative Writing, Computer Science, or related field 2-5+ years working as a Technical Writer, preferably in the IT/Software industry 1-3+ years providing technical support in the ...

Air Methods

Technical Writer

Englewood, CO

$64K - $80K/yr

Provide quoted hours for assigned work tasks * Other duties as assigned. Additional Job ... Experience with CAD software (SolidWorks and AutoCAD preferred) and data vault and management ...

Sidram Technologies

Technical Writer

Santa Clara, CA · On-site

Bachelor's degree in Technical Communication, Computer Science, or a related field * 2-5 years of experience in technical writing or documentation (experience may vary by role level) * Strong written ...

Astrion

Technical Writer

Warner Robins, GA

Strong organizational skills and ability to multi-task * Strong technical, analytical and ... Technical writers will also apply writing skills and an understanding of the appropriate equipment ...

Astrion

Technical Writer

Warner Robins, GA · On-site

Strong organizational skills and ability to multi-task * Strong technical, analytical and ... Technical writers will also apply writing skills and an understanding of the appropriate equipment ...

Stratolaunch

Technical Writer

Mojave, CA · Hybrid

$65K - $105K/yr

Excellent organization and multi-tasking skills. * First-rate attention to detail. * Ability to ... Experience with XML structured authoring tool REQUIRED COMPUTER SKILLS * MS Office (Word, Excel ...

Tech Digital Group

Technical writer

Libertyville, IL · On-site

MSAT Technical Writer, Cell Therapy Vector Support ,Support, Manufacturing Science and Technology (MSAT) The focus of the MSAT Technical Writer is to investigate and write root cause analyses for non ...

Astrion

Technical Writer

Warner Robins, GA · On-site

Strong organizational skills and ability to multi-task * Strong technical, analytical and ... Technical writers will also apply writing skills and an understanding of the appropriate equipment ...

JMA Solutions

Technical Writer

Oklahoma City, OK · On-site

DESCRIPTION The Technical Writer will provide trained, skilled, and competent technical writing support to the Program Office, to include support for highly visible tasks that require interfacing ...

vTech Solution

Technical Writer

Richmond, VA · On-site

Bachelor's degree in English, Technical Communication, Computer Science, or a related field * 5+ years of experience in technical writing, preferably in a government or technology environment

Kratos Defense

Technical Writer

Crane, IN

We are seeking a highly motivated technical writer to join our Kratos Defense & Rocket Support ... Ability to manage multiple tasks and meet deadlines in a fast-paced environment * Strong ...

ClifyX

Technical Writer

Church Road, PE · On-site

CA$61/hr

The Technical Writer will be provided a desk (work area), computer, and standard office supplies while working for PPL EU. The term of work could be for up to two years, but may be cancelled at any ...

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Technical Writer

Tech Digital Group

Bothell, WA • On-site

Contractor

Re-posted 19 days ago

Job description

Job Title: Technical Writer
Schedule: M-F, Normal business hours, 100% Onsite
Top Skills:
• Bachelor's degree in a relevant scientific field (e.g., Biology, Chemistry, Life Sciences) or equivalent combination of education and experience preferred.
• Proven experience as a technical writer or in a related role within a clinical laboratory or regulated environment.
We are seeking a highly skilled and detail-oriented Technical Writer to join our dynamic clinical laboratory team. The ideal candidate will be responsible for creating, reviewing, and maintaining comprehensive and accurate documentation related to configuration specifications, impact assessments and clinical lab deviations.
This role requires a strong understanding of laboratory practices, regulatory requirements, and the ability to communicate complex information clearly and concisely.
Key Responsibilities:
1. Documentation Development:
o Write, edit, and maintain Standard Operating Procedures (SOPs), Work Instructions (WIs), and guidelines related to clinical lab deviations and impact assessments.
o Prepare deviation reports, impact assessment documents, and corrective and preventive action (CAPA) plans in accordance with regulatory standards and company policies.
2

Deviation Management:
o Collaborate with laboratory staff, quality assurance, and regulatory affairs teams to document and assess deviations in laboratory processes and results.
o Analyze data related to deviations and their impacts, ensuring all relevant information is captured for reviews and audits.
3. Impact Assessment:
o Conduct thorough impact assessments for deviations reported, ensuring that risk is evaluated and documented effectively.
o Facilitate cross-functional meetings to gather insights from relevant stakeholders when assessing the impacts of laboratory deviations.
4. Regulatory Compliance:
o Stay up to date with industry regulations and best practices regarding clinical laboratory operations and ensure all documented processes comply with regulatory requirements.
o Participate in internal audits and inspections, providing necessary documentation and supporting information as needed.
5

Training and Support:
o Collaborate with training departments to develop training materials and conduct training sessions related to deviation reporting and impact assessment processes.
o Provide support and guidance to laboratory personnel regarding documentation requirements and processes.
6. Continuous Improvement:
o Assist in process improvement initiatives by identifying documentation gaps and recommending enhancements to existing processes.
o Monitor trends in deviations and impact assessments to propose strategies for mitigation and risk reduction.
Qualifications:
• Bachelor's degree in a relevant scientific field (e.g., Biology, Chemistry, Life Sciences) or equivalent combination of education and experience preferred.
• Proven experience as a technical writer or in a related role within a clinical laboratory or regulated environment.
• Familiarity with regulatory guidelines (e.g., CLIA, CAP, ISO) and quality management systems.
• Excellent written and verbal communication skills; ability to convey complex information clearly and concisely.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Proficiency in technical writing tools and software (e.g., Microsoft Office Suite, other documentation tools).
Preferred Qualifications:
• Experience in performing root cause analysis and risk assessments related to laboratory deviations.
• Knowledge of laboratory information management systems (LIMS) and related software.
• Certification in technical writing or related fields

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About Techdigital

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TechDigital™ Group is a provider of Total Talent Management Solutions, headquartered in Burnsville, Minnesota. We service the USA, Canada and India geographies with offices in the respective locations. Diversity, Equity and Inclusion is our core part of the hiring process everyday and we strive to fulfill our customers diversity and inclusion goals with our expert teams.

Industry

Recruiting and staffing services

Company size

201 - 500 Employees

Headquarters location

Burnsville, MN, US

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