As a Senior Quality Engineer at Cytiva, you will lead quality management processes and collaborate with cross-functional teams to ensure compliance and excellence in life sciences and biotechnology. This role offers the chance to make a meaningful impact by supporting critical projects that save lives.
Key Responsibilities
Act as a subject matter expert for Change Management/Change Control
Establish and maintain processes and procedures within the Quality System
Collaborate with stakeholders across 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) planBonus/incentive pay