Sr Engr Design Quality
Sr Engr Design Quality
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Job Description
This is where you save and sustain lives
At Baxter we are deeply connected by our mission. No matter your role at Baxter your work makes a positive impact on people around the world. Youll feel a sense of purpose throughout the organization as we know our work improves outcomes for millions of patients.
Baxters products and therapies are found in almost every hospital worldwide in clinics and in the home. For over 85 years we have pioneered significant medical innovations that transform healthcare.
Together we create a place where we are happy successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining liveswhere your purpose accelerates our mission.
Summary:
Lead and support PDLM deliverables review and approval.
Provide process consultancy to the R&D teams.
Essential Duties and Responsibilities:
- Ensures that activities within the Product Development elements are performed in a manner consistent with the Design and Development Plan Change Plan and Quality Planning.
- Responsible for Quality Assurance of the Product Development and Lifecycle Management process.
- Responsible for the compliance and approval of PDLM records to Baxter procedures throughout the product lifecycle.
- Collaborate with regulatory affairs as needed to guide teams in meeting quality/regulatory requirements based on the regulatory plan/strategy or assessment.
- Collaborate with teams to provide guidance for meeting Baxter Requirements and External Quality Standards as appropriate.
- Compliance of the Risk Management File.
Qualifications:
- BS engineering and 6 years in related Quality or Engineering field in the medical products industry. ASQ (e.g. CQE CMQ/OE etc. and/or Six Sigma certification highly preferred
- Strong interpersonal/communication/influencing/negotiation skills.
- Strong analytical and problem solving skills.
- Working knowledge of FDA Regulations and Design Controls requirements.
- Demonstrated ability to lead others within small project or investigational environments.
- Good understanding of 21 CFR Part 820 ISO 13485 EU MDD / EU MDR.
- Broad working knowledge of Medical Device Software Development Lifecycle and IEC 62304.
- Good understanding of medical device manufacturing process.
- Good Understanding of requirements for Calibration and Qualification of Test & Measurement equipment in labs used for Verification and Validation.
Education and/or Experience:
BS engineering and 6 years in related Quality or Engineering field in the medical products industry.
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.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams where fraudulent parties pose as Baxter employees recruiters or other agents and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself review our Recruitment Fraud Notice.
Required Experience:
Senior IC
Employment Type
Full-Time
