Onsite QA Specialist – GLP & Compliance

Zachary Piper Solutions

Rockville (MD)

On-site

USD 39,000 - 43,000

Full time

14 days+
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Benefits offered by this job

Medical
Dental
Vision
401K
PTO
Sick Leave
Holidays

Job summary

Piper Companies in Rockville, MD is seeking a Quality Assurance Specialist for a fully onsite role with a CRO partner. The position focuses on reviewing processes, data records, and documentation to ensure adherence to internal standards and regulatory requirements.

The ideal candidate holds an Associate’s or Bachelor’s degree in Biological or Regulatory Sciences, with 1+ year of quality experience and strong teamwork. GLP experience is preferred; comprehensive benefits are included.

Qualifications

  • Associate’s or Bachelor’s degree in Biological or Regulatory Sciences.
  • 1+ years of quality experience.
  • Efficiently works well with a team environment.
  • GLP experience preferred.

Responsibilities

  • Conduct reviews of operational processes, documentation, data records, and project-related materials to ensure adherence to internal standards and organizational requirements.
  • Support quality, compliance, and continuous improvement initiatives across the organization.
  • Analyze and interpret data from various systems to identify trends, inconsistencies, and opportunities for improvement.
  • Utilize electronic systems and databases to access, validate, and evaluate business records and information.
  • Monitor updates to industry practices, regulations, and guidance to support ongoing compliance efforts.

Skills

Quality Assurance
Teamwork
Data analysis
Documentation review

Education

Associate’s or Bachelor’s degree in Biological or Regulatory Sciences

Job description

Piper Companies in Rockville, MD is seeking a Quality Assurance Specialist for a fully onsite role with a CRO partner. The position focuses on reviewing processes, data records, and documentation to ensure adherence to internal standards and regulatory requirements.

The ideal candidate holds an Associate’s or Bachelor’s degree in Biological or Regulatory Sciences, with 1+ year of quality experience and strong teamwork. GLP experience is preferred; comprehensive benefits are included.

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