Quality Control Deviation Writer (3-6 Month Contract)

Rentschler

Milford, MA, United States
Base: $40ph - $55ph; bonus/equity: not specified; ...
Gmp deviation investigation
Corrective and preventive actions
Root cause analysis expertise
Rentschler Biopharma is a leading CDMO focused exclusively on client projects and advancing medicine to save lives

Job Summary

  • Rentschler Biopharma is a leading CDMO focused exclusively on client projects and advancing medicine to save lives.
  • The QC Deviation Writer is responsible for investigating, writing, and resolving GMP deviations while ensuring compliance with regulatory requirements and maintaining high quality standards.
  • The team culture is built on trust, respect, integrity, and a quality mindset emphasizing reliability, efficiency, and honest feedback.

Matching Summary

Rentschler Biopharma is a leading CDMO focused exclusively on client projects and advancing medicine to save lives.

Salary

Base: $40/hr - $55/hr; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • GMP deviation investigation
  • Corrective and preventive actions
  • Root cause analysis expertise
  • Technical writing in GMP environment
  • Regulatory compliance adherence
  • Cross-functional collaboration
  • Quality management system metrics

Nice-to-have

  • Self-motivated and accountable
  • Excellent organizational skills
  • Effective communication skills
  • Ability to multi-task
  • Quality mindset
  • Fast paced CDMO environment
  • Team-oriented work ethic

Key Requirements

  • Bachelor's degree in scientific discipline
  • Minimum 3 years technical writing experience
  • Experience in regulated GMP environment
  • Strong knowledge of FDA, EMA, ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter