Assoc Prop/Asset Mgmt Anlyst

Northrop Grumman Northridge , CA 91324

Posted 2 months ago

At Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems in air and space that impact people's lives around the world today, and for generations to come. Our work preserves freedom and democracy, and advances human discovery and our understanding of the universe. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have a lot of fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history.

Northrop Grumman Innovation Systems is seeking a Property/Asset Management Analyst to manage and analyze activities associated with asset business systems to ensure company, customer and US Government property located on site and at subcontractors are managed in accordance with applicable regulations and policies to achieve best value and operational excellence.

Job Responsibilities:

Candidate will be responsible for analyzing data, preparing and submitting DD 250's in WAWF, DD 1149's, arranging disposal of plant clearance cases through DCMA eTools, coordinating contract property closeout activities, and performing property management database administration functions.

Candidate will also perform multiple functions including but not limited to physical inventory, as well as records and reports for certain programs. Listed below are various functions and tasks for this position:

  • Provide various material and tagged asset reports.

  • Maintain property accountability records

  • Assist in Contractor Self-Assessment Audits

  • Provide guidance on contracts and regulations pertaining to property life-cycle management

  • Develop, recommend and implement property management policy

  • Additional assignments may be given to assist other team members as necessary

Basic (Required) Qualifications:

  • Bachelor's degree

  • A minimum of 2 years related Property/Asset Management experience

  • Strong verbal and written communication skills and excellent follow up.

Preferred Qualifications:

  • Knowledge of the Government Property Clause FAR 52.245-1

  • NPMA Certifications (CPPS, CPPA, CPPM)

  • Costpoint user experience

  • Procurement Integrated Enterprise Environment user experience

  • AssetSmart user experience

Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/AA and Pay Transparency statement, please visit www.northropgrumman.com/EEO. U.S. Citizenship is required for most positions.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Assoc Biomedical Engineer

Medtronic Inc.

Posted 3 days ago

VIEW JOBS 4/17/2019 12:00:00 AM 2019-07-16T00:00 Careers that Change Lives This position is within Continuous Glucose Monitoring (CGM) Sensor R&D team. The individual will be supporting multiple phases of product development. The individual will work closely with the CGM organization to ensure compliance within all aspects of the CGM product lifecycle. This will include but not limited to, working on CAPA related activities, continuously reviewing and updating compliance SOPs to be in line with industry standards, supporting data integrity programs, and providing compliance support. A Day in the Life * Support CGM functional groups in the development, implementation, and maintenance of compliance activities. * Perform CAPA investigations, action execution, effectiveness determination, associated decisions and documentation * Responsible for all aspects of GLP compliance for the lab including but not limited to, creating, maintaining and implementing SOP's, instrumentation validation/calibration and record keeping. * Author Test Reports and route documents for approval (strong writing skills) * Prepare, test, verify test equipment and ensure proper calibration * Capable of developing fixtures, test equipment and test methods to meet engineering requirements * Generate and analyze test data, and report results per departmental procedures * Assist in the development and implementation of SOPs related to medical device vigilance, product complaints, design controls, medical inquiries, process validations, etc. * Drafting and generating written documentation in the form of specifications, engineering reports, validation plans, and validation reports. * Provide engineering support for Process Validations, Test Method Validations, Verification and Validation strategies, protocols, reports, etc. * Review Design History Files and Technical Files for conformance to applicable requirements. * Support development of Department Operating Procedures (DOPs) that enable Medtronic Diabetes to achieve quality and compliance metrics with domestic and international regulations. * Resolves non-compliance issues; recommending product and process changes; initiating engineering change orders. * Designs, develops and provides safety testing, repair, and maintenance of biomedical equipment. * Ensures that the biomedical equipment is in compliance with applicable regulatory requirements and quality control standards. * Design studies and conduct research on enzyme reactions and the effects of organic compounds on biological processes. * Participate in activities such as compound screening and compound optimization programs and developing and running enzyme assays. Must Have: Minimum Requirements IN ORDER TO BE CONSIDERED FOR THIS POSITION, THE FOLLOWING BASIC QUALIFICATIONS MUST BE EVIDENT ON YOUR RESUME Education Required * Bachelor's degree in the Sciences or Engineering Specialized Knowledge or Skills Required * Experience in using Statistical analysis tools Nice to Have * Experience in MiniTab statistical analysis software; * Technical writing experience with investigations, change requests, standard operating procedures, protocols, etc. * Understanding of CFR 21 820 FDA Quality System Regulation, GMP, ISO 14971 Risk Management, ISO 13485, EU Medical Device Directives and other applicable quality system regulatory standards. * Prior experience driving compliance initiatives within the R&D environment * Knowledge of standards, including (ISO) 11607, EN 60601, IEC 62366, ASTM F2097, ASTM F1980, ASTM D4169, ISTA standards, etc. * Previous experience in performing process validation, including IQ, OQ, and PQ for medical devices. * Knowledge of Hazardous substance regulations (RoHS, REACH, WEEE, etc.). * Excellent written and verbal communication * Ability to prioritize workload, meet multiple deadlines simultaneously in a fast -paced environment 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) Medtronic Inc. Northridge CA

Assoc Prop/Asset Mgmt Anlyst

Northrop Grumman