Lead several moderate projects for multiple products
Independently plans, schedules and leads cross-functional team in detailed phases of the Quality work in a project
Identifies and manages continuous improvement projects with the objective of achieving quality, reliability and/or complaint reduction
Lead audit ready status efforts for assigned areas and assist other areas in understanding FDA, ISO and Baxter quality requirements
Take lead role in NCR/CAPA activities such as investigation, implementation, or verification of effectiveness
Support risk management activities as they relate to product and post market surveillance
Provide product quality support on new product development, risk management, design transfer and sustaining engineering
Work collaboratively with R&D to develop Product Design Requirement and & Test Methods for successful Design Verification and Validation
Defend/support product design history file (DHF) in internal and external audits
What you'll bring
Bachelor’s degree in engineering and minimum three years’ experience in Quality, Manufacturing, and/or Engineering in the Medical Device and/or Biologics/Therapeutics field
Product development experience with medical devices preferred
Proficient in relevant products or process development processes (i.e. NPD and sustaining-life cycle management)
Must have experience with Design History File (DHF) and Risk Management File (RMF)
Demonstrate leadership skills to handle sustaining product support activities involving Complaint investigations, Trigger evaluations and Design Change controls
Good project management skills
Ability to coordinate and present technical and project mgt. overviews without assistance
Solid understanding of FDA Regulations (e.g. 21 CFR Part 820), Application of Good Laboratory Practices, Application of Good Manufacturing Practices, ISO (e.g. ISO13485 and ISO14971) and other applicable standards (e.g. IEC60601 and IEC62304 electromechanical medical device) and regulatory requirements (e.g., EU MDD and MDR)
This role gives you the scope of a global healthcare organisation while keeping your contribution close to the work, customers and products it supports. If the Senior Design Quality Engineer role matches your experience and the kind of responsibility you are looking for, we’d like to hear from you
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The minimum salary for this position is €32.000 annually. Your initial pay could be at the minimum or higher based on skills and expertise, experience, and other relevant factors, all of which are subject to change. This position may also be eligible for competitive benefits, discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
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