Technical Writer
Actalent
Lexington, KY (In Person)
$57,963 Salary, Full-Time
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Job Description
Lexington, KY Location:
Lexington, KY Employment Type:
6 month Contract, First shiftIndustry:
Manufacturing & Life Sciences Overview Our client, a leading manufacturing and life sciences organization, is seeking a Technical Writer to develop, revise, and maintain high‑quality technical documentation within a regulated environment. This role collaborates closely with Engineering, Quality, Regulatory, R D, and Operations teams to ensure documents are accurate, compliant, and easy for end users to understand. If you are detail‑oriented, skilled at translating complex technical information, and experienced with controlled documentation, this opportunity may be an excellent fit. Key Responsibilities Develop, write, edit, and maintain technical documentation including: SOPs Work instructions Manuals Validation documents Training materials Translate complex technical, scientific, and manufacturing concepts into clear, concise, user‑friendly documents. Collaborate cross‑functionally with Engineering, Quality, Regulatory, Manufacturing, and R D teams to gather information and validate accuracy. Ensure all documentation meets applicable regulatory, quality, and internal standards. Manage document revisions, version control, and change documentation within controlled document systems. Support internal and external audits by ensuring documentation is accurate, current, and properly organized. Maintain templates, formatting standards, and writing guidelines to ensure consistency across all technical documentation. Required Qualifications Bachelor's degree in Technical Writing, English, Communications, Engineering, Science, or a related field. 2+ years of technical writing experience in a manufacturing, regulated, or technical environment. Demonstrated ability to produce clear, well‑organized, and user‑focused technical documentation. Experience creating and maintaining SOPs, work instructions, and other controlled documents. Proficiency with Microsoft Word and document management systems. Exceptional attention to detail and the ability to manage multiple documentation projects simultaneously. Preferred Qualifications Experience working in regulated environments (e.g., FDA, GMP, ISO ). Exposure to life sciences, food safety, diagnostics, laboratory operations, or manufacturing processes. Familiarity with electronic document management systems (EDMS) or quality management systems (QMS) . Strong collaborative skills with both technical and non‑technical stakeholders.Key Skills Technical Writing SOP Development Regulatory Documentation Document Control Editing & Proofreading Work Instructions Technical Communication Engineering/Scientific Documentation Top Skills:
Technical writing, SOPs, Regulatory, Document control, Editing Job Type & Location This is a Contract position based out of Lexington, KY. Pay and Benefits The pay range for this position is $20.00 - $30.00/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 onsite position in Lexington,KY.
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