Qa Technician

Cytiva

Fajardo, Puerto Rico
Base: $17.00ph; bonus/equity: eligible for bonus/i...
On-site
Create and review official documentation
Process and retain manual documents
Manage documentation organization and retrieval
Cytiva is seeking a QA Technician for their Fajardo, Puerto Rico location. The role focuses on ensuring accurate documentation and compliance with quality assurance standards in the life sciences field while promoting a culture of continuous improvement

Job Summary

  • The QA Technician is responsible for assuring that all official documentation for Cytiva, Puerto Rico site, third parties and any additional applicable site are created, reviewed, and distributed to ensure accuracy, completeness and adherence to policies, procedures, and regulations.
  • Responsible for the process and record retention of manual documents such as but not limited to batch records, validations, engineering studies, risk assessments.
  • At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

Matching Summary

Match Score: 75

Cytiva is seeking a QA Technician for their Fajardo, Puerto Rico location. The role focuses on ensuring accurate documentation and compliance with quality assurance standards in the life sciences field while promoting a culture of continuous improvement.

Salary

Base: $17.00/hr; Bonus/Equity: Eligible for bonus/incentive pay; Benefits: Comprehensive package including paid time off, medical/dental/vision insurance and 401(k)

Skills & Requirements

Must-have

  • Create and review official documentation
  • Process and retain manual documents
  • Manage documentation organization and retrieval
  • Update and retrieve information from Quality System
  • Create and process labels

Nice-to-have

  • Continuous improvement culture
  • Innovate for tangible impact
  • Work with people that care

Key Requirements

  • Bachelor’s degree in business administration, Science or related fields
  • 2-4 years of clerical/secretarial experience in Documentation or manufacturing
  • Ability to interpret and apply rules, regulations, policies, and procedures
  • Knowledge of GMP’S, QSR, ISO and FDA regulations
  • Computer proficiency (ERP, EDM, MS Office, SAP, Veeva)

Work Rights

Not specified

Tailored Resume

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