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Form of workAt Getinge we have the passion to perform
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our passion is to secure that every person and community have access to the best possible care, offering hospitals and life science institutions products and solutions that aim to improve clinical results and optimize workflows. Every day we collaborate to make a true difference for our customers - and to save more lives.
Are you looking for an inspiring career? You just found it.
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Manager, Supplier Quality Control (MAQUET Cardiovascular, LLC; Wayne, New Jersey): Reports to Director Supply Chain;; responsible for managing the Quality Control of suppliers who provide raw material for our product manufacturing; plan, direct and coordinate the quality of our suppliers' program including formulating company Quality Control policies and procedures; leads the CS/VI Supplier Quality program and executes associated systems, processes, programs/initiatives, practices, and metrics for ensuring and improving overall Supplier Quality performance; partners with quality leaders as well as representatives from Sourcing/Supply Chain, R & D, Operations, and other functions to lead and collaborate on Supplier Quality Management improvements. Duties include: developing and managing the department to assess and ensure compliance to the FDA Quality System Regulations CFR Part 820, ISO 13485 Quality System Standard, MDD, CMDR, WHLW, ANVISA, JPAL and other applicable regulations; leading the Supplier Quality team and coordinating efforts to evaluate, select, qualify, rate, monitor and improve Supplier Quality; ensuring that Supplier Quality personnel maintain the required skill level to address compliance issues and to understand the technical aspects of compliance; developing risk based programs for supplier qualifications and supplier performance and productivity improvement; creating benchmark/reports that measure and track Supplier Quality performance to identify opportunities for improvements; overseeing validations and qualifications of supplier facility to qualify manufacturing processes and overall quality of part/component manufacturing; and responsible for supporting the Incoming Inspection Process.
Telecommuting permitted up to 3 days a week. During any internal or FDA audits, the employee may be requested to be on site 5 days a week.
Minimum requirements: Bachelor's degree or foreign equivalent in Chemistry, Biochemistry, or related Life Sciences field or equivalent, plus two (2) years of experience in a Supplier Quality engineering role.
Must have: Must have a strong background in administering Supplier Corrective Action Programs, supplier audit process, and PPAP (Production Part Approval Process).
Send resume to: Lesa Vazquez, Manager, Human Resources, MAQUET Cardiovascular, LLC., 45 Barbour Pond Drive, Wayne, New Jersey, 07470. Ref: 00052027. An EOE.
About us
Getinge is on an exciting transformation journey constantly looking for new ways to innovate together with our customers to meet the healthcare challenges of the future. Our passionate people hold our brand promise 'Passion for Life' close to heart.
If you share our passion and believe that saving lives is the greatest job in the world, then we look forward to receiving your application and resume. We hope you will join us on our journey to become the world's most respected and trusted MedTec company.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our passion is to secure that every person and community have access to the best possible care, offering hospitals and life science institutions products and solutions that aim to improve clinical results and optimize workflows. Every day we collaborate to make a true difference for our customers - and to save more lives.
Are you looking for an inspiring career? You just found it.
Online Advertisements
Manager, Supplier Quality Control (MAQUET Cardiovascular, LLC; Wayne, New Jersey): Reports to Director Supply Chain;; responsible for managing the Quality Control of suppliers who provide raw material for our product manufacturing; plan, direct and coordinate the quality of our suppliers' program including formulating company Quality Control policies and procedures; leads the CS/VI Supplier Quality program and executes associated systems, processes, programs/initiatives, practices, and metrics for ensuring and improving overall Supplier Quality performance; partners with quality leaders as well as representatives from Sourcing/Supply Chain, R & D, Operations, and other functions to lead and collaborate on Supplier Quality Management improvements. Duties include: developing and managing the department to assess and ensure compliance to the FDA Quality System Regulations CFR Part 820, ISO 13485 Quality System Standard, MDD, CMDR, WHLW, ANVISA, JPAL and other applicable regulations; leading the Supplier Quality team and coordinating efforts to evaluate, select, qualify, rate, monitor and improve Supplier Quality; ensuring that Supplier Quality personnel maintain the required skill level to address compliance issues and to understand the technical aspects of compliance; developing risk based programs for supplier qualifications and supplier performance and productivity improvement; creating benchmark/reports that measure and track Supplier Quality performance to identify opportunities for improvements; overseeing validations and qualifications of supplier facility to qualify manufacturing processes and overall quality of part/component manufacturing; and responsible for supporting the Incoming Inspection Process.
Telecommuting permitted up to 3 days a week. During any internal or FDA audits, the employee may be requested to be on site 5 days a week.
Minimum requirements: Bachelor's degree or foreign equivalent in Chemistry, Biochemistry, or related Life Sciences field or equivalent, plus two (2) years of experience in a Supplier Quality engineering role.
Must have: Must have a strong background in administering Supplier Corrective Action Programs, supplier audit process, and PPAP (Production Part Approval Process).
Send resume to: Lesa Vazquez, Manager, Human Resources, MAQUET Cardiovascular, LLC., 45 Barbour Pond Drive, Wayne, New Jersey, 07470. Ref: 00052027. An EOE.
About us
Getinge is on an exciting transformation journey constantly looking for new ways to innovate together with our customers to meet the healthcare challenges of the future. Our passionate people hold our brand promise 'Passion for Life' close to heart.
If you share our passion and believe that saving lives is the greatest job in the world, then we look forward to receiving your application and resume. We hope you will join us on our journey to become the world's most respected and trusted MedTec company.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
- Health, Dental, and Vision insurance benefits
- 401k plan with company match
- Paid Time Off
- Wellness initiative & Health Assistance Resources
- Life Insurance
- Short and Long Term Disability Benefits
- Health and Dependent Care Flexible Spending Accounts
- Commuter Benefits
- Parental and Caregiver Leave
- Tuition Reimbursement
Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law.
