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1+ months

Configuration Assurance Analyst

Northridge, CA 91325
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Configuration Assurance Analyst


Northridge, California, United States

Requisition #:


Post Date:

Nov 11, 2020

**Careers That ChangeLives**

This role is a
member of the Diabetes Group Configuration Management/ Document Control
Department and serves as liaison to the global Medtronic Product Lifecycle
Management team. Through this relationship this person will receive the
tools, training and support necessary to ensure that the practices he/she is
following at the local site are in line with global Medtronic master data
practices. This is what ensures our master data is consistent, complete and
viable throughout Medtronic.


Transforming diabetes care together, for greater freedom and better

Our strategy is to
become a holistic diabetes management company focused on making a real
difference in outcomes and cost. We want to transform healthcare toward
value-based models by driving both product and business model innovation with
the goal of elevating patient experience, improving clinical outcomes and
lowering the total cost of care for our customers.

We value what makes
you unique. Be a part of a company that thinks differently to solve problems,
make progress, and deliver meaningful innovations.

Visit to see an overview of the products in our Diabetes product

**A Day in the Life**

**Responsibilities may include thefollowing and other duties may be assigned.**

+ Processchange orders in compliance with applicable procedures that support compliancewith regulations and standards pertaining to medical device quality systemchange management.

+ Providedirection and guidance in the change order process and work with changeoriginators to maintain clear, concise and valid documents throughout.

+ Collaboratewith stakeholders and change originators.

+ Processparts and documents changes in a timely manner according to requirements andprocedures to support business requirements.

+ Driveand facilitate in a timely manner the change, approval and release ofdocumentation according to project schedules, including the resolution ofresource issues relative to the processing of document change orders.

+ Responsiblefor data entry integrity when transferring changes to product data in multiplesystems.

+ Responsiblefor ensuring that the best practices of Part/Document Change Management arefollowed.

+ Monitorparts and documents changes management process effectiveness and contribute toproblem solving/continual improvement discussions regarding change controlprocess, including the impact of changes and takes the initiative to recommendprocess improvements.

+ Participatein department meetings and performs other tasks and related duties as assigned.

**Must Have: MinimumRequirements**

**Tobe considered for this role, please ensure the minimum requirements are evidenton your resume.**

with 2+ years of work experience in Quality or regulated industry OR Advanced
degree with 0+years of work experience in Quality or regulated industry

**Nice to Have**

+ Proficientusing the following software systems: Agile and SAP.

+ Certificatein CM2 Configuration Management.

+ Excellentanalytical, verbal communication and writing skills.

+ Abilityto work in a team environment as well as independently and with minimalsupervision.

+ Exhibitshigh degree of initiative and good judgment.

+ Knowledgeablein using Agile PLM Import Tool and competent in Agile searches.

+ Abilityto communicate in writing clearly and concisely, using excellent grammar andsentence structure.

+ Knowledgeof product(s) design and assembly to make informed decisions aboutconfiguration management so that the documentation is efficient and complete.

+ Experiencein the manufacture and development of product, preferably medical devices.

+ Experiencewith and understanding of medical device quality systems.

+ Abilityto read design and manufacturing drawings and documents.

+ Skilledin tasks associated with document handling, archiving and change management.

+ Strong attention to detail and accuracy.

+ Strongtime management, organizational, and prioritization skills.

+ Abilityto effectively manage multiple projects and priorities.

+ Abilityto interface professionally at all levels of the organization.

**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. Lets work together to address universal healthcare needs and improve
patients lives. Help us shape the future.

**Physical JobRequirements**

The 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 Day in the Life
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.
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.


Posted: 2020-11-13 Expires: 2021-03-05
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