Join Cytiva as a Senior Quality Engineer and lead quality assurance processes that save lives in life sciences and biotechnology. Collaborate across teams to innovate and ensure compliance while enhancing your career in a culture that values your unique perspective.
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 (e.g. GMP medical device, pharmaceutical)
At least 5 years relevant QMS experience with 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)
Experience with risk management (FMEA)
Analyzing and processing data with statistical tools
Experience working with cross-functional teams
Benefits & Perks
Paid time offMedical, dental, and vision insurance401(k) planBonus/incentive pay