Senior Quality Engineer

By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.

At Integer, our values are embedded in everything we do.

Customer

We focus on our customers' success

Innovation

We create better solutions

Collaboration

We create success together

Inclusion

We always interact with others respectfully

Candor

We are open and honest with one another

Integrity

We do the right things and do things right

Who are we?

Integer is a global organization providing innovative, high-quality technologies and manufacturing to Medical Device OEM's (original equipment manufacturers) to enhance the lives of patients worldwide and a provider of high-end niche batteries for specialized applications in the energy, military, and environmental markets. We are guided by our six Values, including focus on Customers, Innovation, Collaboration, Inclusion, Candor, and Integrity. Working at Integer means you are part of a team passionately pursuing excellence in all that we do and always reaching for the next great achievement.

What you'll do in this role:

The primary purpose of this position is to apply intensive and diversified knowledge of Quality Systems Management principles and practices in broad areas of assignments and related fields. You will ensure that Integer internal and external customers' expectations are met or exceeded.

* You will adhere to Integer's Values and all safety, environmental, security and quality requirements including, but not limited to: Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements.

* You will monitor compliance with company policies and procedures and support Quality Audits (Internal and External) activities, including auditing and providing support to address nonconformities.

* You will be responsible for Quality metrics preparation and reporting, including metrics for Supplier performance.

* You will drive continuous QMS improvement by developing procedures and gaining alignment across multiple functional departments.

* You will participate in developing and executing mitigation strategies to reduce risk associated with critical and high-risk suppliers.

* You will play an active role in Supplier management program by identifying the quality system needs for qualifying and monitoring suppliers.

* You will champion the development of and deployment of the Quality Systems tools to drive innovation and continuous improvement.

* You will investigate and interpret internal or external Quality and Regulatory requirements and recommend best practices to the organization.

* You will provide QMS support throughout the organization, including QMS training, and assisting with management and execution of CAPAs, NCs, complaint investigations, SCARs, etc.

* You may lead cross-functional teams or projects with moderate resource requirements, risk and or complexity and may influence others to achieve goals.

* As a subject matter expert in Quality Systems requirements, you may deploy your expertise across multiple locations. As a result, occasional travel may be required in this position.

* You perform other duties, as needed, and as directed by your line of supervision.

How you will be measured:

The specific measures listed below may be subject to change and are not intended to be an all-inclusive list:

* Safety is our highest priority; you will be an active supporter of the Integer Environmental, Health & Safety programs.

* You will have defined Goals and Objectives specifying key projects and expected milestones to achieve.

* Given your capabilities and experience, you will be expected to identify ways to lead systemic changes to current processes and procedures that enable greater efficiencies.

* Innovation and creativity are critical aspects of your role, and you will be expected to generate continuous improvement suggestions and support their implementation.

* You will support a culture of quality and continuous improvement throughout the organization to ensure achievement of Global Quality KPI's and goals.

* Your expertise coupled with your accomplishments and collaboration with others to deliver results will also be considered.

What sets you apart:

* You have earned, as a minimum, a bachelor's degree in Science/Engineering discipline or related technical field or have 10+ years experience in a similar role.

* You are technically seen as a subject matter expert, a recognition you have earned through 7+ years of progressive Quality Systems in the Medical Device, Pharmaceutical, or other regulated industry.

* You have strong knowledge of regional and international quality system requirements including 21 CFR 820, CFR Part 11, ISO 13485, EU MDR, MDSAP, and cGxP for Medical Devices

* Must have a strong understanding of quality system requirements and how each quality system element connects to another.

* You have strong medical device Quality System and Supplier Quality management background. * You are proficient in Microsoft Office applications.

* You have a strong technical and problem-solving foundation, and preferably training and certifications, in a variety of problem-solving and project management methodologies such as 6-Sigma (green belt as a minimum, black belt preferred), 8D, RCA, 5-Why, Ishikawa (Fish Bone).

* You work independently as well as collaboratively with cross functional teams.

* You will demonstrate the ability to lead projects activities and act as a coach for other less experienced associates.

* Clear and professional communications to all levels of the organization are important in this role and you will have well-developed written and oral communication skills.

* You possess a positive, can-do attitude with an underlying belief that failure is not an option.

U.S. Applicants: EOE/AA Disability/Veteran