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Are you looking for a career that matters?We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. We’re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.https://www.youtube.com/watch?v=X0h0ih8MgQEssential Duties and Responsibilities
Manage supplier quality program activities including supplier qualification/evaluation, SCAR investigations, assessment of supplier Notifications of Change, and supplier audits.
Support qualification of new suppliers and materials/services for product launches and processes/projects to ensure completion of project milestones
Lead/Assist with investigations related to raw materials/components. Work with suppliers to ensure thorough investigations and root cause analysis and monitor effectiveness of corrective actions
With minimal guidance, schedules and leads team through the planning and execution of projects
Work with suppliers to apply process capability studies and understand and evaluate material manufacturing processes
Employ appropriate techniques and methods to successfully and independently execute/support material qualification projects. Make technical recommendations regarding material qualification projects.
Identify opportunities for improving existing raw material quality and impact on the manufacturing processes. Develop appropriate raw material specifications with critical to quality characteristics
May be assigned other duties, as needed
Travel to supplier sites may be required
Develops and administers budgets, schedules and performance requirements. Coordinates activities of personnel in other departments and contractors as well as providing day to day guidance to the supplier and incoming staff. Acts as advisor to subordinates to meet schedules and/or resolve technical problems.
Qualifications
Strong interpersonal skills and great attention to details are necessary.
Must have strong technical understanding of medical device and pharma regulatory requirements
Must be a strong team player with good problem solving, and good verbal and written communication skills.
Must be able to handle multiple projects concurrently and work effectively and efficiently with a cross-functional team
Display a solid understanding of theories/practices utilized by other disciplines outside of primary area of expertise
Must be able to provide solutions that reflect understanding business objectives and cost implications. Demonstrated success in delivering results on technical challenges
Ability to develop and present a course of action with minimal assistance using both written and verbal methods
Ability to prioritize multiple tasks and work in a fast-paced environment with accountability for deadlines
Knowledge of statistical analysis tools
Education and/or Experience
BS in Science or Engineering.
6 to 8 years of experience in Quality related function and Supplier Quality with a Medical Device/Pharma company or other similarly regulated industry.
2 years supervision experience
Physical Demand:
Regular attendance is required to perform the essential functions of the job.
Light work, may require lifting; frequent sitting/standing.
Working Environment:
Minimal to moderate travel required.
Normal office working conditions: computer, phone, files, fax, copier.
Personal Protective Equipment: safety glasses as required
Equal Employment OpportunityBaxter 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.EEO is the Law at http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdfEEO is the law - Poster Supplement at http://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCPEEOSupplementFinalJRFQA508c.pdfPay Transparency Policy at https://www.dol.gov/ofccp/pdf/pay-transp%20EnglishformattedESQA508c.pdfReasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to AmericasTTA@baxter.com and let us know the nature of your request along with your contact information.Our products and therapies touch the lives of millions of people around the world every day, which is why we are focused on transformative innovations that bring smarter, more personalized care to all of us. For 87 years and counting, we have been at the critical intersection where the ideas that save and sustain lives meet the providers who make it all happen. And now, we are determined to realize our boldest opportunities to transform global healthcare for years to come.
Vacancy expired!