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Document Review Associate Jobs in Wisconsin (NOW HIRING)

Tax Senior Associate

Madison, WI · On-site

$82K - $101K/yr

... returns Review associates' and interns' tax returns, providing constructive feedback to ensure ... document reviews Strong verbal and written communication skills to effectively interact with ...

Tax Senior Associate

Madison, WI · On-site

$75 - $110/hr

... returns Review associates' and interns' tax returns, providing constructive feedback to ensure ... document reviews Strong verbal and written communication skills to effectively interact with ...

Tax Senior Associate

Madison, WI · On-site

$82K - $101K/yr

... returns Review associates' and interns' tax returns, providing constructive feedback to ensure ... document reviews Strong verbal and written communication skills to effectively interact with ...

Experience with batch record reviews and audits. * Ability to manage document control and change ... Associate degree from an accredited institution is required. * Bachelor's degree in Biology ...

WI · On-site

$65 - $95/hr

Clinical Research Associate - Full-Service Updated: Yesterday Location: Remote, VT, United States ... Conducts Source Document Review of appropriate site source documents and medical records. Verifies ...

WI · On-site

$70 - $110/hr

Clinical Research Associate - Full-Service Updated: Yesterday Location: Remote, TX, United States ... Conducts Source Document Review of appropriate site source documents and medical records. Verifies ...

Produce Department Manager

Portage, WI · On-site

$38K - $38K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Portage, WI · On-site

$38K - $38K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Portage, WI · On-site

$38K - $38K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Eau Claire, WI

$35K - $36K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Eau Claire, WI · On-site

$35K - $36K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Eau Claire, WI · On-site

$35K - $36K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

Eau Claire, WI · On-site

$35K - $36K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Produce Department Manager

West Allis, WI · On-site

$35K - $35K/yr

Maintain proper food safety documentation, verify temperature and sanitation logs, and enforce company safety policies. * Maintain timekeeping accuracy: Review associate schedules and time records ...

Showing results 21-40

Document Review Associate information

What is a document review associate?

A Document Review Associate is a legal professional responsible for examining and analyzing documents relevant to legal cases, investigations, or regulatory matters. They typically review emails, contracts, and other records to determine their relevance, confidentiality, or privilege in the context of litigation or compliance. Document Review Associates often work for law firms, corporations, or third-party vendors and may use specialized software to organize and tag documents for legal teams. This role requires strong attention to detail, understanding of legal concepts, and the ability to handle large volumes of information efficiently.

What are the key skills and qualifications needed to thrive as a document review associate?

To thrive as a Document Review Associate, you need strong analytical skills, attention to detail, and a legal background—often with a JD or paralegal certification. Familiarity with e-discovery platforms like Relativity, Concordance, or Everlaw is commonly required. Excellent organizational abilities, time management, and clear written communication are standout soft skills in this role. These skills ensure accurate, efficient document analysis and compliance with legal standards in high-volume, deadline-driven environments.

What are some common challenges faced by document review associates, and how can they be managed effectively?

Document Review Associates often encounter challenges such as managing large volumes of data, meeting tight deadlines, and maintaining accuracy under pressure. It is essential to develop strong organizational skills, attention to detail, and familiarity with review platforms. Regular communication with team leads and colleagues can help clarify expectations and address any uncertainties, while staying updated on best practices ensures efficiency and quality in the review process.

What are the most commonly searched types of Document Review jobs in Wisconsin?

The most popular types of Document Review jobs in Wisconsin are:

What cities in Wisconsin are hiring for Document Review Associate jobs?

Cities in Wisconsin with the most Document Review Associate job openings:

Associate Manager, Document Control

Merz North America

Franksville, WI • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

About Us

Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history. As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine. Our purpose is to fuel confidence by helping people look better, feel better, and live better. We believe you do not have to choose between living life and making a living. Live your best life with Merz Aesthetics.

A Brief Overview

The Associate Manager, Document Control is responsible for providing tactical and strategic leadership for the Document Control Specialists and the process for the review and approval for Merz QMS Documents. Day-to-day activities include coordination, management and review of the document control team and their activities. Perform and/or assist with tasks required to oversee the proper creation, revision, approval and release of documents in accordance with the Merz QMS, regulations and standards. Oversee and/or assist with tasks related to the activities associated with operation of Merz North America Inc. Quality System and as directed. Provide direct support to Quality Management/Quality Assurance personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed.

What You Will Do

  • Management Manage Document Control department and personnel. Leverage the Document Control team to ensure that business goals, deadlines and performance standards are met.
  • Document Control Ensure all aspects of the Document Control Function effectively and efficiently meet global standards and regulations.
  • Adherence to Regulations and Standards Maintain awareness of changes to global regulatory requirements and relevant standards related to Quality Systems and support the appropriate requirement or standard owner to ensure effective implementation. Support Training activities. Support Training activities including: maintaining training records, supporting Department Training Coordinator (DTC) program, conducting organization wide training (as needed), assists with on-time training goals, conducts orientation for new personnel (iMERZion), and reviewing DCN training plans.
  • Process Improvement Initiatives Drive continuous improvement initiatives / projects for the Quality Systems Department
  • Supports Internal, External and Vendor Audit Functions Supports Internal, External and Vendor Audit Functions as needed

Minimum Requirements

  • Bachelor's Degree
  • 3-5 years Quality experience in Medical Device, Pharmaceutical and/or equivalent regulated industry
  • 2+ years Supervisor or Lead Experience

Preferred Qualifications

  • ASQ CQA or CMQ/OE

Technical & Functional Skills

  • Knowledge of regulatory requirements for medical device / pharmaceutical organization required.
  • Strong technical and general problem-solving skills; experience with NCR/CAPA processes
  • Medical and/or scientific terminology
  • Professional phone etiquette plus careful handling of sensitive information
  • Computer skills in Microsoft Word, Excel, PowerPoint, Visio and Access; Adobe; and Quality System Management Software.
  • Familiar with ISO 13485 Quality System Standards, FDA Quality System Regulations, GMPs, and/or other international medical device regulations
  • Organized, attention to detail
  • Highly effective communication skills. Ability to work with company staff and communicate effectively throughout the organization.
  • Manage multiple priorities and work with interruptions.

Benefits

  • Comprehensive Medical, Dental, and Vision plans
  • 20 days of Paid Time Off
  • 15 paid holidays
  • Paid Sick Leave
  • Paid Parental Leave
  • 401(k)
  • Employee bonuses
  • And more!

Your benefits and PTO start the date you're hired with no waiting period!

This position is not eligible for employer-sponsored work authorization. Applicants must be legally authorized to work in the United States without the need for current or future employer-sponsored work authorization.