Sr Quality Assurance Specialist

Evonik Industries AG

Birmingham, AL, United States
Hybrid
Quality management system documentation
Risk management
Statistical analysis
This position is responsible for providing quality and technical support to the production team providing oversight to manufacturing rooms and laboratories by reviewing and approving data and all other Quality Management System documentation

Job Summary

  • This position is responsible for providing quality and technical support to the production team providing oversight to manufacturing rooms and laboratories by reviewing and approving data and all other Quality Management System documentation.
  • At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues.
  • Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork.

Matching Summary

This position is responsible for providing quality and technical support to the production team providing oversight to manufacturing rooms and laboratories by reviewing and approving data and all other Quality Management System documentation.

Skills & Requirements

Must-have

  • Quality Management System documentation
  • risk management
  • statistical analysis
  • product and process-related documentation
  • Deviation / CAPA investigations
  • root cause analysis
  • product quality and System improvements
  • risk assessment activities
  • cGMP and/or QSR quality system requirements

Nice-to-have

  • hybrid and flexible working environments
  • fresh perspective
  • develop your strengths
  • break out your mold
  • interdisciplinary teams
  • Regulatory Agency inspections
  • aseptic techniques and manufacturing

Key Requirements

  • Bachelor of Science degree in Chemistry, Biology, or Engineering
  • Minimum eight years’ experience in pharmaceutical or medical device manufacturing
  • Minimum five years’ experience in a pharmaceutical or medical device Quality Assurance role
  • Proficient computer skills, Microsoft Word, Excel, Access
  • Applied statistics experience
  • Validation experience, including process validation
  • Advanced analytical and problem-solving skills

Work Rights

Not specified

Tailored Resume

Cover Letter