Quality Assurance Manager
- Location: Chicago, Illinois
- Working Situation: Onsite
- Level: Mid-Senior level
Our client, a leading CRO with over 30 years of experience, skilled researchers provide cutting-edge expertise in small and large molecule bioanalysis to optimize drug development for pharmaceutical companies. We offer bioanalysis for non-clinical and clinical projects, both GLP and non-GLP, to meet critical drug development milestones. With a GLP-compliant state-of-the-art facility has the capacity to accommodate quick turnaround and high-volume projects from around the country.
Quality Assurance Manager
The Quality Assurance Manager is responsible for providing leadership in the development and implementation of an independent quality system to support bioanalytical lab operations. Identify areas of regulatory risk and bring these to the attention of lab management and senior management. Responsible for developing and executing training for all employees on quality assurance policies, programs, initiatives and GLP regulatory requirements.
The Quality Assurance Manager will:
- Lead an effective QA team to ensure lab operations are in compliance with GLP requirements
- Responsible for Quality aspects of Sponsor visits/audits and preparation/ issue of report of such visits/audits ensuring completion of any actions.
- Responsible for document control and quality improvements
- Provide training in GLP for the Bioanalytical department and support departments (where applicable)
The Quality Assurance Manager has the following qualifications:
- 3 years of people management experience (required).
- 3 years of working in a GLP environment and 2+ years working in QA related role
- Bachelor's Degree with relevant fields and experience in pharmaceutical or bio laboratory
Company Benefits:
- A competitive salary
- PTO, company health care plan, medical, dental, and vision insurance
- Short and long-term disability insurance, life insurance policy
- 401k
- opportunities for continuing education.
