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Sr Director Manufacturing Quality – Northridge

 

Sr Director Manufacturing Quality – Northridge

 Northridge, California, United States          ·         Full time

 

Locations: Northridge, California, United States • United States

Job ID: 2300005I

 

Job Description

Careers that Change Lives

The Sr Director of Quality – Site Lead has responsibility for leading operations quality and the deployment of quality systems at the Diabetes plant in Northridge, CA.

This position acts as liaison with OU’s, and other sister manufacturing facilities within the Platform to drive quality management strategies and activities resulting in the highest level of product quality and compliance. Emphasis will be on first time quality and continuous improvement of processes and systems and the execution of site quality strategies through direct accountability and influence within the operations organization.  This position provides leadership and resources to ensure compliance with all elements of the quality management system throughout the organization and ensuring quality system performance is measured and routinely reported/ escalated to executive management

 

A Day in the Life

Responsibilities may include the following and other duties may be assigned.

  • Develops and deploys Quality and Compliance strategies that are aligned with Medtronic’s strategy across areas of responsibility.
  • Reviews, directs and manages manufacturing QA strategies, organization, and execution for results. Ensures that approaches are innovative, industry leading, and meeting the needs of customers and OU business strategies.
  • Collaborates with the operations teams as well as other internal and external partners to ensure the strategy is executed to achieve significant and measurable results.
  • Develops and maintains appropriate communications between OU’s to deliver on Medtronic’s overall quality and operations needs worldwide, collaborating as appropriate to ensure synergies with and between organizations to leverage a harmonized approach whenever possible.
  • Proactively manages quality assurance and compliance activities in order to produce the highest quality products and prevent defects.
  • Creates a culture of continuous learning across areas of responsibilities where root causes on quality issues are identified and organizational learning is institutionalized.
  • Ensures effective processes are established within the organization to monitor quality and compliance execution. Implement proactive and preventive strategies for the resolution of quality and compliance opportunities.
  • Assures the processes used in the manufacturing of products are properly developed, characterized, qualified, and validated to assure the highest possible quality and to ensure an uninterrupted supply of quality product to meet the needs of our customers.
  • Assures that manufacturing quality and performance data are comprehensively measured, trended, reported, and acted on in a timely manner to ensure compliance and support continuous improvement. Ensures constant vigilance in line rejects, manufacturing related field returns of those products and changes to manufacturing process to assure the highest possible quality.
  • Creates a world class Quality organization ensuring top talent is hired, developed, and retained.
  • Lead the strategic planning efforts for area of responsibilities in the Annual Operation Plan (AOP).

 

Must Have: Minimum Requirements 

  • Bachelors degree required
  • Minimum of 15 years of Quality/Engineering experience with 10+ years of managerial experience , or Advanced Degree with a minimum 13 years prior quality/engineering experience, minimum of 10 years of managerial experience

 

Nice to Have

  • Experience in Medical, Pharma or high reliability product industry
  • Experience in multiple Quality related functions
  • Highly results oriented and focused on business priorities
  • Strong leadership and influencing skills to drive results in a highly matrixed organization
  • Strong Business and Quality perspective
  • Strong change management and transformation skills
  • Strong understanding of Process Validation and statistical methods
  • Excellent Communication/Presentation Skills
  • Excellent Interpersonal and Talent Management skills

 

Supplier Controls process knowledge & experience

 

About Medtronic

Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life.  We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. 

We want to accelerate and advance our ability to create meaningful innovations – but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future. 

 

Physical Job Requirements 

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. (ADA-United States of America)

 

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. Learn more about our benefits here.

MIP Eligible: This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) here.

LTI Eligible: This position is eligible for an annual long-term incentive plan. Learn more about Medtronic Long-Term Incentive Plan (LTIP) here.

The provided base salary range is used nationally (except in certain CA locations). The rate offered is compliant with federal/local regulations and may vary by experience, certification/education, market conditions, location, etc.

Min Salary: 193200
Max Salary: 289800
Travel: Yes, < 25 % of the Time

 

Please click here to apply.

 

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