Material Coordinator V Job at Baesystems (San Diego)

Maritime Certification Lead

BMT is a leading global consultancy in design, engineering, science, and risk ma...

Location

Australia , Perth; Sydney; Melbourne

Salary:

Not provided

BMT

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering or a related technical field
Proven experience in Material Certification or Verification & Validation (V&V) within a Defence context
Understanding of the Naval technical regulatory environment and seaworthiness principles
Strong attention to detail with the ability to manage complex documentation hierarchies
Security Clearance: Must hold or be eligible to obtain an Australian Defence Security Clearance (NV1 minimum)

Job Responsibility

Develop and manage the Class Certification Plan, providing oversight of certification activities to ensure sustained compliance with Navy, regulatory, and statutory requirements throughout the in‑service lifecycle
Establish and maintain the Class Certification Basis, ensuring it remains current, configuration‑controlled, and reflective of approved requirements and the material state of Class assets
Act as the single point of contact for all Class certification matters, coordinating engagement with Navy certification authorities, Defence engineering authorities, regulators, and industry partners
Define and manage certification and regulatory requirements for the Class systems and sub‑systems, including certification methods, assurance activities, and evidence expectations
Assure ongoing materiel conformity through configuration management, certification surveillance, configuration audits, and assessment of engineering changes against the Certification Basis
Manage and review certification evidence, ensuring Objective Quality Evidence (OQE) is complete, traceable, and sufficient to support certification decisions and seaworthiness assurance

What we offer

Remote, hybrid, and part-time work options
Competitive salary offering
Performance bonuses
Companywide bonuses
Defence Reserve Leave
24/7 Employee Assistance Program (EAP)
Investment in learning and development

Head of Mechanical Engineering

Ommo is the pioneer of permanent magnet-based 3D tracking technology, providing ...

Location

United States , Carrollton

Salary:

120000.00 - 140000.00 USD / Year

Ommo Technologies

Expiration Date

Until further notice

Requirements

2-3 years of Senior Level Mechanical Engineering Experience
or related discipline
3-5 years of Engineering Leadership Experience
5+ years of relevant experience in medical device design/manufacturing or similar fields
Bachelor’s degree in Mechanical Engineering or related fields
Experience and skills in conflict resolution & team leadership
Lead engineer or manager for product(s) that made it to series production
Proficiency in 3D CAD design, FEA, and 2D drafting/ drawings
Experience with medical device design & manufacturing documentation throughout the product development process
Experience with ISO 13485 or equivalent quality system requirements (e.g., regulated or compliance-driven environments)

Job Responsibility

Lead the technical direction and execution of the mechanical design lifecycle from concept and prototyping through validation and release
Lead the design and prototyping of test fixtures and equipment for R&D and production
Create and review engineering drawings with a focus on GD&T best practices
Perform detailed engineering analyses (including stress, thermal, wear, and tolerance stack-ups) using FEA and hand calculations
Own complex 3D CAD design efforts
Conduct rigorous design reviews
Provide technical mentorship and guidance to mechanical engineers
Model technical excellence through hands-on contributions
Drive team performance by setting clear objectives, managing workloads, and providing regular feedback
Collaborate closely with cross-functional teams

What we offer

Equity
Paid Time Off
Medical, Dental & Vision
401K & 401K Matching

Fulltime

Manager Materials Planning

The Materials Planning Manager will manage, guide and develop all Supply Chain f...

Location

United States , Bridgewater

Salary:

105000.00 - 123000.00 USD / Year

Nestle Health Science

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Supply Chain Management, Procurement, Business Administration or in a related field required
Master’s degree preferred
5+ years of relevant work experience in Supply Chain Management including Supply Planning and/or Procurement required
2+ years of People Leadership experience in leading, motivating, coaching and influencing teams and direct reports is required
Procurement or in a related field required, preferably in a Manufacturing or Factory-based environment in the CPG, Pharmaceutical or Nutraceutical industries
Demonstrated fluency in MS Office (Word/Outlook/PowerPoint) and also in MS Excel (V-Lookups, Pivot Tables, Charts, Graphs, etc.) required
Must possess excellent communication (oral and written), organizational, time management and stakeholder management skills (including the ability to develop and maintain strong, cross-functional stakeholder relationships)
Strong analytical aptitude with a proven ability to both analyze and interpret data, story tell and build quantitative models of business problems required
Willing and able to work under pressure to meet tight deadlines and business priorities with minimal supervision and lead through change management/business transformation required
Must possess creative thinking skills and problem-solving skills to solve key business challenges

Job Responsibility

Serve as the Vitamins, Minerals and Health Supplements (VMHS) Center of Supply functional expert for all MRP related systems and processes
Develop and facilitate implementation of strategic roadmap for Materials Scheduling initiatives and projects
Act as liaison between factory, Procurement, Technical and Production, Transportation, Technical Applications Group, Supply Planning, etc. to drive cross-functional process improvements
Create and maintain training documentation and plans materials scheduling
Serve as escalation point for critical MRP-related process and system issues
Monitor packaging stock levels and lead stock policy discussions with Factories
Monitor health of MRP master data (e.g., safety stock, safety time, GRPT) in factories and work with Materials Schedulers to continuously improve and optimize scheduling/plans
Run MRP health checks and work with factory teams to address corrective
Own and continuously improve process and tools to mitigate expiring materials risk
Monitor Material Requirements Accuracy (MRA) and coordinate with both the Procurement and Planning teams to address major opportunities

What we offer

401(K) with a company match
healthcare coverage
a broad range of other benefits
performance-based incentives
competitive total rewards package

Fulltime

Bim Manager

Workshop/APD is an award-winning, multidisciplinary architecture and design firm...

Location

United States , New York

Salary:

115000.00 - 130000.00 USD / Year

Workshop/APD

Expiration Date

Until further notice

Requirements

Degree in Architecture, Engineering or Design required
6 to 10 years’ experience as a BIM operator preferably with luxury residential, hospitality, and high-end development projects
Certified Autodesk Revit professional
familiarity with Dynamo and Revit API, Rhino is preferred
Proven experience creating template files, custom families, LOD based assets, and managing a firmwide library
Strong competency in Navisworks, BIM 360, BIM Collaborate Pro, Dynamo, and familiarity with SketchUp, Enscape, D5, V-ray
Expert level construction materials, building assemblies, case work and building products required
Experience with managing workflows and collaborating in a team environment with attention to details
Excellent leadership, communication, and ability to mentor teams

Job Responsibility

Manage model health to facilitate the development of architectural working drawings in coordination with project teams
Manage template family, and content development, including advanced parametrics and automation
Develop and maintain project BIM Execution Plans and ensure that deliverables are aligned as required
Oversee the Workshop/APD’s ACC data environment
Facilitates internal training, BIM audits, and model reviews
Establish BIM documentation processes, procedures, workflows, and best practices
Coordinates with project teams to ensure BIM models meet QA/QC standards and client requirements

What we offer

medical
vision
profit sharing 401(k) plan
short- and long-term disability
commuter benefits
IDP mentorship and ARE/AXP reimbursement
discretionary bonus
personal time off (vacation, sick, holidays, and personal days)
comprehensive health and wellness program including discounts, education, prevention training, health coaching, and fitness classes
in-office perks including an employee lounge and rooftop, outdoor patio for lunches, and office supplied food and beverages

Production Planner

Production Planner is responsible for scheduling and monitoring the production p...

Location

South Korea , Pyeong-Taek

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

Bachelor’s Degree or above in Engineering, Supply Chain, Logistics, Business or related field
5~10 years of experience with planning and logistic processes within production environment, preferably in semiconductor equipment industry or a similar high-tech environment
Experience with ERP systems, preferably Oracle
Experience with of Microsoft tools, especially Outlook, Teams, Excel and Power Point
Experience in stakeholder management and driving change
Knowledge and understanding of the following theories: APICS CPIM, MRP, JIT, Kanban and Lean Manufacturing.
Experience in the areas of cycle time reduction, process flow and cost optimization
Good Excel skills including the ability to work with extremely large data sets, Pivot Tables and v lookups.
Excellent written and verbal communication skills in Korean and English
Team player with good social skills who is able to achieve personal and team goals

Job Responsibility

Scheduling raw materials delivery and set internal build, testing and reclaim plan to meet central demand plan
Manages manufacturing work orders to drive weekly build schedule to released configurations.
Analyzes and reports material shortages and impacts to ship schedule.
Recommends reclaim forecast adjustments based on actual performance.
Coordinating production workflow for multiple products
Inventory control for stock materials and ensure that material transactions are done accurately
Monitoring part structures (BoMs and Routes) for errors and initiating corrections.
Determining raw materials needed and manage stock levels to meet production demand
Manage flow of incoming and outgoing material from suppliers to deliver on time.
Perform cycle counts and variance investigations in line with the company count policy and calendar

Fulltime

Senior Mechanical Design Engineer – Space Payloads

Our client, a growing NewSpace startup, is seeking a Senior Mechanical Design En...

Location

Germany , Berlin

Salary:

Not provided

NewSpace Technical

Expiration Date

Until further notice

Requirements

BSc in Mechanical Engineering with 7+ years experience (or MSc/PhD with 5+)
Strong CAD experience (e.g. SolidWorks, CATIA, Fusion)
Experience with mechanical and opto-mechanical design for space applications
Experience leading or supporting space qualification campaigns
Knowledge of FEM, structural dynamics, resonant modes, lightweight structures, and thermal/mechanical deformation
Experience translating system-level requirements into mechanical designs
Familiarity with GD&T standards (e.g. ISO GPS)
Strong written and verbal communication skills in English
Fluency in English (C1 or higher)
Willingness to relocate to Berlin (EU work authorisation is a plus)

Job Responsibility

Lead mechanical and opto-mechanical design of a space payload from concept through detailed design, build, AIT, and deployment
Perform mechanical design, analysis, documentation, fabrication support, assembly, and qualification activities
Design structures such as optical benches, opto-mechanical assemblies, mechanisms, and electronics packaging (PCBs, connectors, harnessing) using CAD tools
Work hands-on with technicians during assembly, integration, and test
Lead vibration and acoustic qualification campaigns and support thermal-vacuum testing
Collaborate closely with cross-functional teams across systems, optics, thermal, and mission engineering
Develop and maintain mechanical documentation including architectures, ICDs, assembly procedures, and V&V plans
Interface with suppliers and external vendors for parts and manufacturing
Coordinate with spacecraft bus teams to ensure clean mechanical and structural interfaces
Prepare material for major design reviews (PDR, CDR, MRR, FRR) and provide RFP cost inputs

Fulltime

Sr Hardware Quality Engineer

This position performs various quality-engineering functions and associated supp...

Location

United States , Louisville, KY; Vernon Hills, ILLINOIS

Salary:

48.00 - 52.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BS in Engineering, Engineering Technology, Science a minimum
American Society of Quality (ASQ) certification (CQE, CQA, CQM, etc.) preferred
Minimum 1 year of experience with FDA regulated industry, preferably on product development programs
Ability to perform detailed engineering work under direction of a Senior Engineer or Quality Management
Understands basic applied statistics
Ability to participate on teams and maintain positive work environment with those teams
Good communication skills (verbal, written, and presentation)
Understands Basic Fundamentals of Engineering Principles
Ability to effectively manage time
Ability to handle multiple task assignments

Job Responsibility

Represents the Corporation, Division and Quality Department in a professional manner as an on-site V. Mueller Quality Representative/Liaison with Owens & Minor Quality Engineering, Operations, and Value-Added Services (VAS) groups
Creates/reviews Protocols, Process and Product Validations as required
Creates and reviews Test Methods and addresses Test Method Validation
Creates and reviews documents required for Design History File
Creates and reviews Risk Assessments such as FMEA, FMECA or FTA
Ensures compliance to V. Mueller Quality Department and BDI- Surgery policies and procedures
Participates and has membership in trade and/or professional organizations to ensure that state-of-the-art industry standards are communicated into the division in an efficient, timely, and accurate manner
Interfaces with V. Mueller manufacturing facilities or other Division Facilities
Supports root cause investigations and other steps of the CAPA process
Travels as required by the above duties and responsibilities

Fulltime

Sr Hardware Quality Engineer

This position performs various quality-engineering functions and associated supp...

Location

United States , Louisville

Salary:

34.00 - 39.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BS in Engineering, Engineering Technology, Science a minimum
Minimum 1 year of experience with FDA regulated industry, preferably on product development programs
Ability to perform detailed engineering work under direction of a Senior Engineer or Quality Management
Understands basic applied statistics
Ability to participate on teams and maintain positive work environment
Good communication skills (verbal, written, and presentation)
Understands Basic Fundamentals of Engineering Principles
Ability to effectively manage time
Ability to handle multiple task assignments
Ability to translate quality requirements into product specifications

Job Responsibility

Represents the Corporation, Division and Quality Department in a professional manner as an on-site V. Mueller Quality Representative/Liaison with Owens & Minor Quality Engineering, Operations, and Value-Added Services (VAS) groups
Creates/reviews Protocols, Process and Product Validations as required
Creates and reviews Test Methods and addresses Test Method Validation
Creates and reviews documents required for Design History File
Creates and reviews Risk Assessments such as FMEA, FMECA or FTA
Ensures compliance to V. Mueller Quality Department and BDI- Surgery policies and procedures
Participates and has membership in trade and/or professional organizations to ensure that state-of-the-art industry standards are communicated into the division in an efficient, timely, and accurate manner
Interfaces with V. Mueller manufacturing facilities or other Division Facilities
Supports root cause investigations and other steps of the CAPA process
Travels as required by the above duties and responsibilities

Fulltime

Material Coordinator V

Baesystems

Location:
United States , San Diego

Category:
Logistics

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 04, 2026

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