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Job Description
Join Cytiva as a Senior Quality Engineer and play a pivotal role in ensuring quality in life sciences and biotechnology. You'll lead initiatives in quality management systems, collaborate with cross-functional teams, and contribute to projects that impact 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 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)
Analyzing and processing data with statistical tools
Working with cross-functional teams
Benefits & Perks
Paid time offMedical/dental/vision insurance401(k) plan