Join Cytiva as a Senior Quality Engineer and play a pivotal role in enhancing life sciences and biotechnology solutions. You will be responsible for quality management systems and lead change control processes while collaborating across teams to ensure compliance and innovation.
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 required
At least 8 years relevant industry experience (GMP medical device, pharmaceutical)
At least 5 years relevant QMS experience (investigations, CAPA, change control, risk management)
Extensive experience with cGMP and/or ISO 13485
Excellent verbal, written, and presentation skills
Preferred Qualifications
Experience with supporting change control systems (ECR / ECO) and risk management (FMEA)
Analyzing and processing data with statistical tools
Working with cross-functional teams to implement solutions
Benefits & Perks
Paid time offMedical/dental/vision insurance401(k)