Join Cytiva as a Senior Quality Engineer and be at the forefront of life sciences innovation. You'll enhance quality systems, lead change management processes, and collaborate with diverse teams to drive real-world impact in health solutions.
Key Responsibilities
Act as a subject matter expert for Change Management/Change Control
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 (e.g. GMP medical device, pharmaceutical)
At least 5 years relevant QMS experience
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 various statistical tools
Working with cross-functional teams to implement solutions
Benefits & Perks
Paid time offMedical/Dental/Vision insurance401(k) planBonus/incentive pay