QA Technician: QC & Documentation in Pharma/Tech

Cryopak-Industries

Roanoke (VA)

On-site

USD 55,000 - 70,000

Full time

7 days ago
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Benefits offered by this job

Medical Insurance
Vision Insurance
Health Savings Account (HSA)
Flexible Spending Account (FSA)
Voluntary Accident, Critical Illness,

Job summary

Cryopak Digital (CVT) in Roanoke, VA is seeking a QA/QC / Quality Assurance Specialist to perform in-production inspections, final QC checks, and support mapping validation activities. You will help maintain the QMS, write protocols, and collaborate with cross-functional teams to ensure compliance with CVT and regulatory requirements.

Your role includes CAPA logging, audit support, and ongoing quality improvements, with up to 50% travel as needed.

Qualifications

  • College diploma in science, industrial pharmaceutical or related discipline (or equivalent experience).
  • 1-3 years’ experience in pharmaceutical/biotechnology/QMS/quality roles (entry to intermediate).
  • ISO 9001 basics: document control, non-conformity & CAPA basics, internal audits.
  • ISO 17025 basics: calibration & traceability, sample handling, QC samples, test reports.
  • QMS maintenance: document control, records, SOPs at basic to intermediate level.
  • Quality mindset: attention to detail, proactive attitude.
  • Experience writing technical protocols and reports.
  • Proficient in Word and Excel; CS monitoring systems.
  • Excellent organizational and prioritization skills; attention to detail.
  • Valid driver’s license; travel up to 50% as needed.

Responsibilities

  • QA/QC inspection: perform quality inspections at Roanoke location to meet internal quality standards.
  • Mapping services: support mapping projects remotely with Montreal team and CVT roadmap.
  • Inspect during production and prior to shipment; document results and deviations.
  • Maintain the QMS with document control, SOP updates, and change control guidance.
  • Assist in continuous improvement of QA/QC processes; suggest template and checklist updates.
  • Record CAPA, track actions, and verify closure with QA Director and teams.
  • Write, review protocols for mapping, validation, and quality activities.
  • Coordinate mapping expectations with MTl site and clients; trend data for projects.
  • Support customer communication and training on mapping activities; assist audits.

Skills

Quality mindset
Technical writing
Organization
Prioritization
Teamwork

Education

Science-related college diploma

Tools

Microsoft Word
Microsoft Excel
Computerized Monitoring System

Job description

Cryopak Digital (CVT) in Roanoke, VA is seeking a QA/QC / Quality Assurance Specialist to perform in-production inspections, final QC checks, and support mapping validation activities. You will help maintain the QMS, write protocols, and collaborate with cross-functional teams to ensure compliance with CVT and regulatory requirements.

Your role includes CAPA logging, audit support, and ongoing quality improvements, with up to 50% travel as needed.

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