We're looking for a Quality Assurance Specialist III, working in the Pharmaceuticals & Medical Products industry in New Haven, Connecticut, United States.
Support daily activities related to processing and maintenance of controlled GMP documents associated with quality system management records (complaints, deviations, CAPA and procedures).
Assist with improvements to applicable standard operating procedures and electronic systems related to the complaint management system.
Assist with reviews and asses deviations; participate in investigating root cause, tracking, following up and reporting/trending.
Assist with analyzing quality system data to measure key performance indicators, identify areas for continuous process improvements and risk mitigation, comply and present analyses at Quarterly Management Review meetings, propose appropriate CAPA.
Assist in creating documents including Standard Operating Procedures.
Provide support for day to day complaint management and reconciliation activities.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelor of Science in a related field
6 - 9 Years of experience
Prior complaint handling experience preferred.
Medical Device experience desired.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.