Quality Specialist

JLL

New Albany, Ohio, United States
Base: $67,000 to $97,000; bonus/equity: 7.5% bonus...
Onsite
Bachelor's degree in scientific or engineering field
3 years experience in pharmaceutical gmp environments
1-2 years experience in quality assurance or regulatory compliance
The Quality Specialist provides comprehensive quality assurance support for facility maintenance operations in a regulated pharmaceutical environment while ensuring compliance with FDA regulations

Job Summary

  • The Quality Specialist provides comprehensive quality assurance support for facility maintenance operations in a regulated pharmaceutical environment while ensuring compliance with FDA regulations.
  • This role requires strong collaboration with JLL leadership and client Quality Assurance to maintain inspection readiness and drive continuous improvement initiatives.
  • JLL offers a supportive culture with comprehensive benefits including a 401(k) plan, paid parental leave at 100% of salary, and early access to earned wages.

Matching Summary

The Quality Specialist provides comprehensive quality assurance support for facility maintenance operations in a regulated pharmaceutical environment while ensuring compliance with FDA regulations.

Salary

Base: $67,000 to $97,000; Bonus/Equity: 7.5% bonus; Benefits: 401(k) matching, medical/dental/vision, paid parental leave

Skills & Requirements

Must-have

  • Bachelor's degree in scientific or engineering field
  • 3 years experience in pharmaceutical GMP environments
  • 1-2 years experience in quality assurance or regulatory compliance
  • Strong documentation discipline and GDP knowledge
  • Ability to conduct self-inspections and audit readiness

Nice-to-have

  • Auditing experience in pharmaceutical manufacturing
  • Experience with documentation control systems
  • Background in facilities maintenance operations
  • Knowledge of Quality Management Systems (QMS)
  • Professional certifications such as ASQ or RAC

Key Requirements

  • Bachelor's degree in scientific, engineering, or technical field
  • Minimum 3 years pharmaceutical/biotech GMP experience
  • 1-2 years QA or regulatory compliance experience
  • Authorized to work in the United States without sponsorship

Work Rights

Must be authorized to work in the US without sponsorship

Tailored Resume

Cover Letter