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Part Time Weekend Document Review Jobs (NOW HIRING)

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Part Time Weekend Document Review information

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$13

$23

$33

How much do part time weekend document review jobs pay per hour?

As of Jul 11, 2026, the average hourly pay for part time weekend document review in the United States is $23.33, according to ZipRecruiter salary data. Most workers in this role earn between $19.71 and $26.92 per hour, depending on experience, location, and employer.

What is the difference between Part Time Weekend Document Review vs Part Time Weekend Data Entry?

AspectPart Time Weekend Document ReviewPart Time Weekend Data Entry
Required SkillsAttention to detail, legal or medical knowledge, document analysisTyping speed, accuracy, basic computer skills
Work EnvironmentHome-based or office, focused on reviewing documentsHome-based or office, focused on entering data into systems
Industry UsageLegal, healthcare, insuranceVarious industries including healthcare, finance, retail
Common Search IntentPart Time Weekend Document Review vs Part Time Weekend Data Entry

Part Time Weekend Document Review involves analyzing and verifying documents, often requiring specific industry knowledge, while Part Time Weekend Data Entry focuses on inputting data accurately into systems. Both roles are flexible, home-based, and suitable for part-time weekend work, but they differ in skills and industry focus.

What cities are hiring for Part Time Weekend Document Review jobs? Cities with the most Part Time Weekend Document Review job openings:
What are the most commonly searched types of Weekend Document Review jobs? The most popular types of Weekend Document Review jobs are:
What states have the most Part Time Weekend Document Review jobs? States with the most job openings for Part Time Weekend Document Review jobs include:

Document Specialist (Part-TIme)

Ursitti Enterprises LLC

Portage, IN

$19 - $20/hr

Part-time

Re-posted 29 days ago


Job description

Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their Portage Facility! If you meet the qualifications below, APPLY NOW!

$20.00/Hour


Job Description:

We seek a meticulous and organized Document Specialist to join our client's team in Portage. As a Document Specialist, you will be crucial in managing and maintaining various documents critical to their operations, including regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other essential records.

Responsibilities:

  • Document Management: Ensure the accurate and timely creation, revision, and maintenance of documents, adhering to established guidelines and regulatory requirements.
  • Quality Control: Perform thorough quality checks on documents to ensure accuracy, consistency, and compliance with internal standards and regulatory guidelines.
  • Document Review: Review documents for completeness, correctness, and clarity, collaborating with relevant stakeholders to address discrepancies or issues.
  • Version Control: Manage document versions effectively, maintaining a clear and organized version history to facilitate tracking and retrieval.
  • Documentation Support: Support various departments by assisting in preparing, formatting, and distributing documents as needed.
  • Training and Compliance: Assist in training employees on document management processes and procedures to ensure compliance with company policies and regulatory standards.
  • Continuous Improvement: Identify opportunities for process improvements and efficiency enhancements within the document management system.

Qualifications:

  • Bachelor's degree or equivalent experience in a relevant field of life sciences, business administration, or related discipline).
  • Previous experience in document management, preferably within the pharmaceutical or healthcare industry.
  • Strong attention to detail and excellent organizational skills, with the ability to effectively manage multiple tasks and priorities.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and document management software.
  • Familiarity with regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GCP, GMP) preferred.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.