Medtronic
Principal Supplier Quality Engineer
Medtronic, Los Angeles, California, United States, 90079
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the LifeThis position will be onsite in Northridge, CA at Medtronic's Diabetes OU.
In this exciting role as a Principal Supplier Quality, you will be working with a team of Supplier Quality Engineers in the West / Mexico region, located at the Northridge, CA manufacturing site as well as team members from other functions such as Process Engineers, Quality Engineers, Production Leads, among others.
You will primarily support the on-going manufacturing operations, sourcing and quality operations, particularly the Receiving Inspection area; work in close collaboration with Suppliers on all Quality related activities such as Root Cause investigations, Corrective Actions, NCMR’s, improvement initiatives such as Kaizen events, Gemba walks, onsite audits, etc. Additionally, you will be the main point of contact and SME for any internal and external audits from the Purchasing Controls standpoint.
You will be accountable for meeting the Supplier Quality Key Performance Indicators (KPI’s) from assigned suppliers such as timely evaluation and closure of Supplier Change Requests (SCR’s), Supplier CAPA’s (SCAPAs), disposition and closure of NCMR’s, as well as maintenance of the Approved Suppliers List (ASL).
Responsibilities may include the following and other duties may be assigned.
Be the main Supplier Quality representative and point of contact at the Northridge site for related meetings and events (Tier 3, Tier 4 meetings, Staff meetings, Management Reviews, Audits etc.)
Lead supplier improvement initiatives such as First Time Quality, Kaizen events, Supplier Owned Quality (SOQ) and Programmatic Saving projects.
Lead on all purchasing controls activities such as the following:
ASL Maintenance
Production Part Approval process (PPAP)
Supplier Performance Monitoring.
Supplier Change Requests (SCR) evaluation.
Plan and execute supplier audits as required.
Supplier CAPAs.
Development of Receiving Inspection plans
Implement, review and update as required local Purchasing Controls procedures and work instructions and assure they are aligned to global Policies.
Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
Selects, develops and evaluates personnel to ensure the efficient operation of the department.
An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies.
Formulates, delivers, and/or manages projects assigned and works with other stakeholders to achieve desired results.
Typically provides guidance, coaching and training to other employees within job area.
Typically manages major / moderately complex projects, involving delegation of work and review of work products, at times acting as a team leader.
Travel up to 25% may be required.
Must Have: Minimum RequirementsTo be considered for this role, please ensure the minimum requirements are evident on your resume.
Bachelor’s Degree required.
Minimum 7 years of relevant Manufacturing (internal & external) Supplier Quality Engineering experience, OR Advanced degree with a minimum of 5 years of relevant Manufacturing (internal & external) Supplier Quality Engineering experience.
Ability to travel up to 25%.
Nice to Have:Preference will be given to applicants who possess the following skills, experiences, and certifications.
Experience in Medical, Pharmaceutical or highly regulated product industry.
DMAIC Lean / Six Sigma Certification and demonstrated experience leading DMAIC Projects.
ISO 13485 / ISO 9001 Lead Auditor certification.
Experience in multiple Quality related functions (Receiving Inspection, Quality Control, etc.).
Highly results oriented and focused on business priorities.
Strong leadership and influencing skills to drive results.
Strong Business and Quality perspective.
Excellent Communication/Presentation Skills.
Excellent Interpersonal and Talent Management skills.
Flexible, able to adapt quickly to change in priorities.
Program Management skills.
Physical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $114,400.00 - $171,600.00. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
About MedtronicWe lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
At Medtronic, most positions are posted on our career site for 3-7 days.
#J-18808-Ljbffr
A Day in the LifeThis position will be onsite in Northridge, CA at Medtronic's Diabetes OU.
In this exciting role as a Principal Supplier Quality, you will be working with a team of Supplier Quality Engineers in the West / Mexico region, located at the Northridge, CA manufacturing site as well as team members from other functions such as Process Engineers, Quality Engineers, Production Leads, among others.
You will primarily support the on-going manufacturing operations, sourcing and quality operations, particularly the Receiving Inspection area; work in close collaboration with Suppliers on all Quality related activities such as Root Cause investigations, Corrective Actions, NCMR’s, improvement initiatives such as Kaizen events, Gemba walks, onsite audits, etc. Additionally, you will be the main point of contact and SME for any internal and external audits from the Purchasing Controls standpoint.
You will be accountable for meeting the Supplier Quality Key Performance Indicators (KPI’s) from assigned suppliers such as timely evaluation and closure of Supplier Change Requests (SCR’s), Supplier CAPA’s (SCAPAs), disposition and closure of NCMR’s, as well as maintenance of the Approved Suppliers List (ASL).
Responsibilities may include the following and other duties may be assigned.
Be the main Supplier Quality representative and point of contact at the Northridge site for related meetings and events (Tier 3, Tier 4 meetings, Staff meetings, Management Reviews, Audits etc.)
Lead supplier improvement initiatives such as First Time Quality, Kaizen events, Supplier Owned Quality (SOQ) and Programmatic Saving projects.
Lead on all purchasing controls activities such as the following:
ASL Maintenance
Production Part Approval process (PPAP)
Supplier Performance Monitoring.
Supplier Change Requests (SCR) evaluation.
Plan and execute supplier audits as required.
Supplier CAPAs.
Development of Receiving Inspection plans
Implement, review and update as required local Purchasing Controls procedures and work instructions and assure they are aligned to global Policies.
Organizes the coordination of activities with outside suppliers and consultants to ensure timely delivery.
Selects, develops and evaluates personnel to ensure the efficient operation of the department.
An individual contributor with responsibility in our technical functions to advance existing technology or introduce new technology and therapies.
Formulates, delivers, and/or manages projects assigned and works with other stakeholders to achieve desired results.
Typically provides guidance, coaching and training to other employees within job area.
Typically manages major / moderately complex projects, involving delegation of work and review of work products, at times acting as a team leader.
Travel up to 25% may be required.
Must Have: Minimum RequirementsTo be considered for this role, please ensure the minimum requirements are evident on your resume.
Bachelor’s Degree required.
Minimum 7 years of relevant Manufacturing (internal & external) Supplier Quality Engineering experience, OR Advanced degree with a minimum of 5 years of relevant Manufacturing (internal & external) Supplier Quality Engineering experience.
Ability to travel up to 25%.
Nice to Have:Preference will be given to applicants who possess the following skills, experiences, and certifications.
Experience in Medical, Pharmaceutical or highly regulated product industry.
DMAIC Lean / Six Sigma Certification and demonstrated experience leading DMAIC Projects.
ISO 13485 / ISO 9001 Lead Auditor certification.
Experience in multiple Quality related functions (Receiving Inspection, Quality Control, etc.).
Highly results oriented and focused on business priorities.
Strong leadership and influencing skills to drive results.
Strong Business and Quality perspective.
Excellent Communication/Presentation Skills.
Excellent Interpersonal and Talent Management skills.
Flexible, able to adapt quickly to change in priorities.
Program Management skills.
Physical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits Package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $114,400.00 - $171,600.00. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
About MedtronicWe lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 90,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
At Medtronic, most positions are posted on our career site for 3-7 days.
#J-18808-Ljbffr