Qa Documentation Specialist I

Kite

Frederick, MD, US
$80,325.00 - $103,950.00; discretionary annual bon...
Onsite (sunday to wednesday, 7:00 am to 5:30 pm)
Electronic document management system (dms)
Document archival
Gmp record support
Kite is seeking a QA Documentation Specialist I to support GMP documentation lifecycle activities within a regulated manufacturing environment in Frederick, MD. The ideal candidate will have relevant industry experience and be responsible for ensuring compliance, accuracy, and inspection readiness of documentation processes

Job Summary

  • The role is responsible for document control, training document readiness, and GMP record support to ensure compliance, accuracy, and inspection readiness at our Frederick, MD facility.
  • This position supports GMP documentation lifecycle activities within a regulated manufacturing environment, reporting to the Sr. Manager, Document Control.
  • The company is dedicated to developing treatments and making advances in cancer therapies, aiming to cure cancer.

Matching Summary

Match Score: 75

Kite is seeking a QA Documentation Specialist I to support GMP documentation lifecycle activities within a regulated manufacturing environment in Frederick, MD. The ideal candidate will have relevant industry experience and be responsible for ensuring compliance, accuracy, and inspection readiness of documentation processes.

Salary

$80,325.00 - $103,950.00; Discretionary annual bonus, discretionary stock-based long-term incentives; Company-sponsored medical, dental, vision, and life insurance plans

Skills & Requirements

Must-have

  • electronic Document Management System (DMS)
  • document archival
  • GMP record support
  • document change control
  • label printing

Nice-to-have

  • evolve culture
  • employee development
  • inclusive environment
  • scientific breakthroughs

Key Requirements

  • Master’s Degree and OR Bachelor’s Degree and 2+ years relevant industry experience
  • AA Degree and 4+ years relevant industry experience
  • High School Degree and 5+ years relevant industry experience
  • Current Good Manufacturing Practices (cGMP) experience
  • Pharma Industry experience

Work Rights

Not specified

Tailored Resume

Cover Letter