2

Part Time Biotech Jobs in Virginia (NOW HIRING)

Parttime | 15 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology ... We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ...

People also search for

Part Time Biotech information

See Virginia salary details

$10.9K

$66.1K

$112.5K

How much do part time biotech jobs pay per year?

As of May 30, 2026, the average yearly pay for part time biotech in Virginia is $66,094.00, according to ZipRecruiter salary data. Most workers in this role earn between $29,700.00 and $89,200.00 per year, depending on experience, location, and employer.

What is a Part Time Biotech job?

A Part-Time Biotech job involves working in the biotechnology field with reduced hours compared to a full-time position. Responsibilities may include lab research, data analysis, regulatory compliance, or assisting in experiments, depending on the specific role. These positions are ideal for students, professionals seeking work-life balance, or those looking to gain industry experience. Part-time roles are available in biotech companies, research institutions, and healthcare organizations.

What are the key skills and qualifications needed to thrive in the Part Time Biotech position, and why are they important?

To thrive as a Part Time Biotech, you typically need a background in biology, chemistry, or a related science, along with hands-on laboratory skills and attention to detail. Familiarity with lab equipment, data analysis software, and safety protocols is often expected, and some positions may require certifications in lab techniques or biosafety. Strong communication, time management, and teamwork skills help you adapt to flexible schedules and collaborate effectively. These qualifications enable you to perform precise experiments, support larger projects, and contribute reliably even in a part-time capacity.

What are some typical responsibilities for a Part Time Biotech employee and how do they fit into the overall research team?

Part Time Biotech employees often assist with routine laboratory procedures such as sample preparation, running experiments, data entry, and maintaining lab equipment. They frequently collaborate with full-time scientists and technicians, providing crucial support that helps keep projects progressing smoothly. Even in a reduced-hour schedule, their work contributes to the efficiency and success of the entire research team. This role is ideal for students, individuals transitioning careers, or professionals who prefer flexible hours, while still allowing for skill development and valuable hands-on experience in the biotech field.
What are the most commonly searched types of Biotech jobs in Virginia? The most popular types of Biotech jobs in Virginia are:
What cities in Virginia are hiring for Part Time Biotech jobs? Cities in Virginia with the most Part Time Biotech job openings:
Medical Records Management Testing & Validation Consultant (Part Time, Remote)

Medical Records Management Testing & Validation Consultant (Part Time, Remote)

TestPros

Sterling, VA • On-site, Remote

Part-time

Posted 5 days ago


Job description

Company Overview:
TestPros is a successful and growing business, established in 1988 to provide Information Technology (IT) technical support services to a wide range of Commercial and U.S. Federal, State, and Local Government customers. Our capabilities include Program Management, Program Oversight, Process Audit, Intelligence Analysis, Cyber Security, NIST 800-53, NIST SP 800-171 / CMMC Consulting/Assessment/Compliance, PCI Compliance, HIPAA, SOC 2, GLBA, Zero Trust, Resiliency, Computer Forensics, Software Supply Chain Assurance, Software Testing, Test Automation, Section 508 and WCAG Accessibility Assessment and Remediation, Localization Testing, Independent Verification and Validation (IV&V), Quality Assurance (QA), Compliance, and Research and Development (R&D) services. TestPros is an Equal Opportunity Employer.
Position: Part time (as needed, 1099 or Corp. to Corp)
Position Summary
We are seeking an experienced Testing & Validation Consultant to support hands-on testing and compliance validation of a medical records management and electronic document management application operating within a regulated healthcare and/or FDA-related environment.
The consultant will perform functional, security, compliance, privacy, and data integrity testing of systems managing sensitive healthcare and electronic records. The ideal candidate will have experience validating applications against regulatory and records management standards including HIPAA, FDA 21 CFR Part 11, ISO 16175-1, and ISO 14641.
This role is focused on practical testing and validation activities rather than high-level IV&V oversight only.
Key Responsibilities
  • Perform hands-on functional testing of medical records management or electronic records applications
  • Execute compliance validation activities related to HIPAA, FDA 21 CFR Part 11, ISO 16175-1, and ISO 14641 requirements
  • Review system functionality related to:
    • Electronic records management
    • Electronic signatures
    • Audit trails and audit logging
    • Access controls and user permissions
    • Encryption and secure transmission
    • Data retention and traceability
    • Privacy and protected health information (PHI/ePHI) handling
  • Develop and execute:
    • Test plans
    • Test cases
    • Validation scripts
    • Traceability matrices
    • Defect reports
    • Compliance validation documentation
  • Validate data integrity, record authenticity, retention, and system security controls
  • Review prior internal validation documentation and enhance or develop updated testing documentation
  • Coordinate with stakeholders to identify testing scope, compliance objectives, and remediation priorities
  • Document findings, risks, gaps, and recommendations
Required Experience
  • Experience testing or validating:
    • Medical records systems
    • Electronic document management systems (EDMS)
    • Electronic health record (EHR/EMR) systems
    • Records archive or controlled electronic records applications
  • Hands-on experience with software testing and validation in regulated healthcare, pharmaceutical, biotech, medical device, laboratory, or records management environments
  • Strong understanding of:
    • HIPAA Privacy Rule
    • HIPAA Security Rule
    • FDA 21 CFR Part 11
  • Experience validating:
    • Electronic records
    • Electronic signatures
    • Audit trails
    • Access controls
    • Security safeguards
    • Data integrity controls
  • Experience developing and executing functional and compliance test cases
  • Ability to analyze regulatory requirements and translate them into testable validation criteria
Preferred Experience
  • Experience with ISO 16175-1:2020 functional requirements for digital records management systems
  • Experience with ISO 14641:2018 electronic document preservation and traceability requirements
  • Experience performing privacy reviews and compliance assessments involving PHI/ePHI
  • Experience supporting FDA-regulated or GxP environments
  • Familiarity with records retention, legal admissibility, and long-term digital preservation requirements
  • Experience supporting validation documentation for audits or regulatory reviews
Testing Areas of Focus
  • Functional testing
  • Security testing
  • Compliance validation
  • Privacy and data integrity review

Performance/load testing is not currently required.
Deliverables
  • Test plans and test cases
  • Validation protocols and scripts
  • Compliance assessment documentation
  • Defect and remediation reports
  • Final validation summary/report

TestPros, Inc. is an Equal Opportunity Employer.
EEO Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, marital status, age, national origin, or protected veteran status.