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Actalent
Quality Documentation Specialist
Career Insights for Document Control / Management Specialist
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Based on Connecticut data
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What they do
A Document Control or Management Specialist manages written and electronic documents for an office or company. Develops or maintains systems for keeping track of documents, including labeling, retrieving, distributing, recovering and destroying documents as needed.
$45,071 / year median in Connecticut
+2% projected growth
Job Description
Quality Documentation Specialist Actalent - 3.5 Middlebury, CT Job Details Temporary | Temp-to-hire $33 - $41 an hour 1 day ago Benefits Commuter assistance Health savings account AD&D insurance Disability insurance Health insurance Dental insurance 401(k) Paid time off Employee assistance program Vision insurance Life insurance Qualifications Technical editing Content creation for technical audiences Regulatory compliance Technical writing experience within manufacturing Manufacturing facility experience Technical writing quality assurance Quality systems Manufacturing Manufacturing company experience
Full Job Description Job Title:
Quality Documentation Specialist Job Description In this role, you will review, edit, and process document revisions, update procedures and work instructions, and ensure all controlled documents comply with quality system requirements. You will collaborate closely with Quality, Regulatory, and Engineering teams to support audits, document control activities, and ongoing compliance initiatives. The ideal candidate will possess experience in a manufacturing environment, strong technical writing skills, and familiarity with quality documentation and regulated industries. Responsibilities Update, revise, and maintain controlled quality and regulatory documents. Manage document changes and revision control. Work with regulatory-driven documents, audits, and compliance requirements impacting documentation. Support Quality, Regulatory, and Engineering teams in compliance initiatives. Essential Skills Experience in a manufacturing environment. Understanding of quality systems, including controlled documentation, procedures, and compliance requirements. Strong technical writing and editing skills. Familiarity with quality documentation and regulatory compliance. Additional Skills & Qualifications ISO / Medical Device Experience is preferred but not required. MDR/MDD Experience is beneficial but not mandatory. Experience with engineering documentation is advantageous. Candidates from aerospace or other highly regulated industries would also be considered. Work Environment This position is onsite from 8 AM to 5 PM. You will work closely with Quality, Regulatory, and Engineering teams in a collaborative environment where employees contribute across multiple functions. Enjoy a supportive culture that values work-life balance, career growth, and employee appreciation, including company-provided lunch every day. Job Type & Location This is a Contract to Hire position based out of Middlebury, CT. Pay and Benefits The pay range for this position is $33.00 - $41.00/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 Middlebury,CT.