Join Cytiva as a Senior Quality Engineer and make a direct impact on life sciences and biotechnology. You will enhance quality management systems and ensure compliance, while collaborating with diverse teams to drive innovation and improve human health.
Key Responsibilities
Act as a subject matter expert for Change Management/Change Control process
Establish and maintain site/business unit level processes and procedures
Collaborate with stakeholders across several business functions
Lead or support quality and compliance projects
Required Qualifications
Bachelor’s degree
At least 8 years relevant industry experience (e.g. GMP medical device, pharmaceutical)
At least 5 years relevant QMS experience dealing with investigations, CAPA, change control, risk management
Extensive experience with cGMP and/or ISO 13485
Excellent verbal, written, and presentation skills in English
Preferred Qualifications
Experience with supporting change control systems (ECR / ECO) and risk management (FMEA)
Analyzing and processing data with various statistical tools
Working with cross-functional teams to identify and implement solutions
Benefits & Perks
Paid time offMedical/dental/vision insurance401(k)