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Document Review Associate Jobs in Colorado (NOW HIRING)

Accuserve

Technical Review Specialist I

Denver, CO · On-site

$19/hr

Receive, enter, and manage insured-hired claims including handling follow-up for documentation ... An associate or bachelor degree is preferable or the equivalent combination of education, training ...

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Document Review Associate information

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 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 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 Colorado? The most popular types of Document Review jobs in Colorado are:
What cities in Colorado are hiring for Document Review Associate jobs? Cities in Colorado with the most Document Review Associate job openings:
Document Review Associate jobs near you

Quality Systems Associate I

UHY Farrelly Dawe White Limited

Centennial, CO • On-site

$25 - $30/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Quality Systems Associate I
Department: Quality
Location: Centennial, CO 80112
Employment Type: Full-Time, PRN
Compensation: $25-30 DOE
Join Our Team as a Quality Systems Associate at VPI Compounding Pharmacy!
VPI Compounding Pharmacy is at the forefront of pharmaceutical excellence and is seeking a detail-oriented, ambitious Quality Systems Associate to join our Quality team. You'll work across departments to support quality systems, compliance, and documentation, gaining hands-on experience in a role critical to patient safety and product quality. If you're curious, detail-oriented, and ready to make an impact, this is your opportunity to grow with a company shaping the future of pharmaceutical care!
Key Responsibilities
Regulatory Compliance
  • Support adherence to USP <795>, <797>, <800>, and FDA compounding regulations.
  • Help prepare for audits and inspections

Quality System Support
  • Assist with maintaining SOPs, change controls, deviations, and CAPAs.
  • Help track and organize training documentation.

Training & Documentation
  • Support technician training and competency checks.
  • Ensure accurate and up-to-date quality records.

Data & Reporting
  • Collect and report basic quality metrics and trends.
  • Participate in improvement initiatives and cross-team projects

Qualifications
Required:
  • Associate's or Bachelor's degree in a STEM field (science, technology, engineering, mathematics).
  • Strong attention to detail and organizational skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Excellent written and verbal communication skills.
  • Proficiency in Microsoft Office (Word, Excel, Outlook).

Preferred:
  • Experience in quality assurance or a related field in pharmaceuticals or healthcare.
  • Familiarity with compounding pharmacy standards and quality documentation.
  • 2+ years of experience in biotechnology, microbiology, biochemistry, or other scientific disciplines.
  • Experience supporting audits or working within regulated environments.

Physical Demands:
  • Must be able to walk, stand, and move between departments for extended periods throughout the workday.
  • Requires extended periods of computer work and document review.
  • Occasional lifting (up to 25 lbs) may be required.
  • Ability to wear appropriate personal protective equipment (PPE) including lab coats, gloves, and masks when in cleanroom or sterile areas.

Benefits:
  • Company-paid health, dental, and vision insurance
  • 401(k) plan with employer match
  • Paid holidays, Floating holidays, and PTO
  • Tuition and Certification Reimbursement Programs
  • RTD EcoPass
  • Opportunities for growth and advancement in a supportive and professional environment

Equal Opportunity Employer:
VPI Compounding Pharmacy is an Equal Employment Opportunity (EEO) employer. We are committed to providing equal opportunity for all qualified persons employed by or seeking employment with VPI, regardless of race, color, creed, religion, sex, sexual preference, national origin, age, marital status, veteran status, or non-job-related handicaps. This policy extends to all areas of employment, including recruitment, job assignment, promotion, and other terms of employment.

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