Qa Technician

Danaher Corp

Fajardo, Puerto Rico, US
Base: $17.00ph; bonus/equity: eligible for bonus/i...
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Bachelor's degree in business or science
2-4 years clerical documentation experience
Knowledge of gmp, qsr, iso, fda regulations
** Cytiva, part of Danaher Corporation, is seeking a QA Technician for their Fajardo, Puerto Rico site, focusing on documentation accuracy and compliance within the life sciences sector. The role involves managing official documentation and ensuring adherence to regulatory standards while fostering a culture of continuous improvement. **

Job Summary

  • The QA Technician is responsible for creating, reviewing, and distributing official documentation to ensure adherence to policies, procedures, and regulations.
  • This role involves managing the process and record retention of manual documents such as batch records, validations, engineering studies, and risk assessments.
  • Cytiva offers a broad array of comprehensive benefits including paid time off, medical/dental/vision insurance, and a 401(k) plan.

Matching Summary

Match Score: 75

** Cytiva, part of Danaher Corporation, is seeking a QA Technician for their Fajardo, Puerto Rico site, focusing on documentation accuracy and compliance within the life sciences sector. The role involves managing official documentation and ensuring adherence to regulatory standards while fostering a culture of continuous improvement. **

Salary

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

Skills & Requirements

Must-have

  • Bachelor's degree in business or science
  • 2-4 years clerical documentation experience
  • Knowledge of GMP, QSR, ISO, FDA regulations
  • Proficiency with MS Office applications
  • Experience with ERP and EDM systems

Nice-to-have

  • Regulatory Affairs knowledge and experience
  • Certified Quality Auditor certification
  • Audit experience
  • Bilingual English and Spanish skills
  • Veeva System knowledge

Key Requirements

  • Bachelor's degree required
  • 2-4 years work-related significant clerical functions
  • General knowledge of GMPs, QSR, ISO, FDA
  • Computer oriented with ERP/EDM knowledge

Work Rights

Not specified

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