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Akkodis is seeking a for a Design Controls Engineer- Medical Device at Location: Santa Clarita CA Hybrid for a contract Duration: 06-Months initially. Pay Range: $70/h- $87/h; The rate may be negotiable based on experience, education, geographic location, and other factors. Location: Hybrid (3 days onsite: Tue/Wed/Thu; Mon/Fri as needed) Position Overview The Design Controls Engineer provides technical and engineering support for design control activities across product development, quality, manufacturing, and project execution. This role requires strong project management, problem‑solving skills, and the ability to work independently while coordinating with internal teams and external suppliers. The engineer will support design verification/validation, test method development, risk management, and manufacturing transfer activities for projects of moderate complexity. Key Responsibilities Design Controls & Product Development • Ensure full compliance with all Design Controls requirements., • Develop and source new requirements, create and validate test methods, and generate new risk documentation., • Perform product testing and document results in alignment with quality and regulatory standards., • Compile, analyze, and report operational, test, and research data to establish performance specifications for new or modified products, processes, and materials. Quality & Compliance • Maintain product safety, quality, and regulatory compliance across all assigned activities., • Apply FDA Quality System Regulations and ISO 13485 standards., • Conduct assessments for quality and compliance impacts on product design or process changes., • Support change management activities (DCA, SCIA, SCAR, PLCP). Manufacturing & Supplier Coordination • Support manufacturing transfers between vendors., • Collaborate with internal stakeholders and external suppliers to plan and execute engineering and quality projects. Tools, Fixtures & Test Method Development • Design and develop tools and fixtures using SolidWorks for test method development and validation., • Utilize MiniTab for data analysis and troubleshooting. Project Support • Support planning and execution of R&D project activities., • Manage multiple concurrent activities under limited supervision., • Support additional business requirements as needed. Required Qualifications • Bachelor’s degree with 5–8 years, Master’s with 3–6 years, or PhD with 0–3 years of relevant experience., • 5+ years experience with design controls., • 5+ years experience working under FDA QSR and ISO 13485., • Strong experience in design verification & validation activities., • Experience in test method development, troubleshooting, and root cause analysis., • Ability to work independently and manage multiple concurrent activities., • Strong writing and verbal communication skills (assessments, protocols, reports, email)., • Working knowledge of MiniTab and SolidWorks. Preferred Qualifications • Led 4+ product design or process change projects., • 3+ years mechanical design experience., • Participation in 4+ new product development projects, including product transfer and scale‑up., • Experience with SAP and Windchill., • Human Factors / Usability Engineering experience. Quality Systems Responsibilities • Embed quality compliance into all work activities and maintain adherence to all applicable quality system requirements. If you feel this is not something that you are currently interested in but know of someone who might be, please share the details with them or let me know their details so I can reach out to them! Here are the specs on the role, for your records: Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ___. The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance

Position: Manufacturing Engineer Location: Valencia, California 91355 Industry: Aerospace Job Summary The Manufacturing Engineer is responsible for developing, standardizing, and maintaining the company’s manufacturing cost structure. This role will lead the transformation from a tribal?knowledge?driven costing approach to a modern, data?driven system that supports accurate quoting, pricing, margin analysis, and operational decision?making. The engineer will also create documentation of part numbering linked to commonality and manufacturing requirements to improve traceability, planning, and manufacturability. This position requires strong analytical capability, deep understanding of manufacturing processes, and the ability to collaborate across Engineering, Operations, Supply Chain, and Finance Education/Previous Experience • 5 to 7 years’ manufacturing engineering, cost engineering, or operations analysis (aerospace preferred)., • Bachelor of Science degree in Mechanical, Manufacturing or Industrial Engineering required, • Strong understanding of BOMs, routings, labor standards, and manufacturing workflows., • Experience with ERP/MRP systems., • Experience in fixture design and automation project success., • Advanced analytical skills; proficiency with Excel, Power BI, or similar tools., • Advanced skills in Solid Modeling (CATIA, AutoCAD, SolidWorks, or similar), • Ability to lead cross?functional initiatives and drive standardization., • Excellent communication skills with the ability to translate technical detail into clear business impact. Qualifications • Experience in aerospace manufacturing or highly regulated environments., • Background in cost modeling, quoting, or pricing., • Familiarity with AS9100 requirements., • Lean or Six Sigma certification. Primary Responsibilities • Develop and optimize manufacturing processes to improve efficiency, quality, and repeatability., • Provide manufacturing engineering support for production operations and new program launches., • Support new product introduction, process validation, and first article inspections., • Design, implement, and support tooling, fixtures, production aids, and automated manufacturing systems., • Lead project management for complex automation and capital projects, including requirements definition, vendor selection, cost justification, and implementation., • Manage external vendors and integrators to ensure automation projects meet technical, schedule, and cost objectives., • Define manufacturing process plans, routings, and BOM structures aligned with actual shop-floor practices., • Establish and validate labor standards, machine rates, setup times, and run times., • Develop and maintain standardized, data-driven manufacturing cost models across product families., • Identify and analyze cost drivers for material, labor, overhead, scrap, yield, and automation ROI., • Partner with Supply Chain to validate purchased part costs and supplier cost drivers., • Partner with Finance to align cost models, capital investments, quoting, pricing, and margin requirements., • Audit existing routings, costs, standards, and automation assumptions to eliminate inaccuracies and tribal knowledge., • Lead root-cause analysis and corrective/preventive actions for manufacturing and automation-related issues., • Drive continuous improvement initiatives using Lean, Six Sigma, and data-driven methods; provide technical support, training, and support special projects as needed.

Job Description MECHANICAL INSPECTOR Location: Valencia, CA 91355 Industry: Aerospace QUALIFICATIONS • Familiarity with AS9102 standards, • 3+ years of precision measurement inspection experience, • Blueprint reading Summary Responsible for performing and recording visual inspection of component level and/or top assembly products. Job Duties and Responsibilities • Required to perform simple product inspections with appropriate supporting documentation verifying actual results against drawing and/or specification requirements with little supervision., • Verify supplier approval status and certifications against drawing and/or specification requirements for accuracy and completeness., • Verify compliance of finished hardware with drawing requirements based on shop practices as they relate to unfinished hardware (e.g., visual verification of machined areas, etc.), • Ability to understand and conform to internal company procedures., • Perform simple mathematic calculations., • Ability to effectively inspect product using basic inspection tools, which may include, but not limited to, micrometers, bore gages, height gages, etc., • Use quality-related software and ERP to appropriately record assigned job results based on completed processes., • Meet deadlines of assigned jobs while maintaining the integrity of the position., • Seek and document lean process improvement ideas., • Execute formal first article reports to AS9102 standards., • Review ATP for accuracy and completeness., • Obtain customer source delegation, as required.Company DescriptionWe're not just a staffing company - we're a people company. At Amtec, we care about helping you reach your unique career goals. Since 1959, we’ve changed the lives of thousands of people for the better - people just like you. It’s our purpose to help you find meaningful work by matching your character, competence, and culture with an organization that truly values what you have to offer.We're not just a staffing company - we're a people company. At Amtec, we care about helping you reach your unique career goals. Since 1959, we’ve changed the lives of thousands of people for the better - people just like you. It’s our purpose to help you find meaningful work by matching your character, competence, and culture with an organization that truly values what you have to offer.

Collaborate with cross-functional teams to resolve supplier-related quality issues, ensuring root cause analysis is performed and corrective actions are tracked to closure. Experienced quality professional ensuring aerospace supplier compliance with AS9100 and ISO 9001 standards. Provide technical s

Job Description Position Summary This position is responsible for supporting the purchasing and procurement process by creating and issuing purchase orders for materials, parts, and services, tracking deliveries, and coordinating with suppliers to ensure timely fulfillment. The Buyer will monitor open orders, confirm lead times, follow up on late shipments, and escalate supply issues to help prevent production delays and reduce disruptions. This role works closely with internal teams such as production, engineering, and quality to align purchasing needs and maintain accurate procurement records in the ERP (Epicor) system. Success in this role requires strong attention to detail, organization, professional communication, and a willingness to learn procurement fundamentals in a fast-paced manufacturing environment. Minimum Qualifications Education: • High school diploma or GED required, • 0–3 years of experience in purchasing, supply chain, manufacturing, or administrative support preferred, • Experience in a manufacturing environment preferred, • Basic understanding of purchasing, logistics, or manufacturing environments preferred, • Strong attention to detail and accuracy, • Strong written and verbal communication skills, • Proficiency in Microsoft Excel and Outlook, • Ability to prioritize multiple tasks and meet deadlines, • Ability to work cross-functionally with internal teams Purchase Order Processing • Create and issue purchase orders for materials, parts, and services, • Ensure PO details are accurate (pricing, part numbers, quantities, ship-to, due dates), • Maintain purchasing documentation and records in the ERP system, • Communicate with suppliers to confirm orders and lead times, • Track open orders and follow up on late or at-risk deliveries, • Escalate supply issues to the Procurement/Supply Chain Manager as needed, • Coordinate with production and planning teams to support material availability, • Partner with engineering and quality teams for supplier or part changes, • Assist with reporting related to spend, supplier performance, and open PO status Physical Requirements The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel, and talk or hear. The employee frequently is required to sit; occasionally required to walk, stoop, kneel, crouch, or crawl; and must occasionally lift and/or move up to 10 pounds. Specific vision abilities include close and distance vision. This position requires the use of information or access to hardware and documents that are subject to the International Traffic in Arms Regulations (ITAR). All applicants must be able to comply with the requirements of ITAR and other U.S. export control laws. Compensation: $24.00 - $29.00 / Hour

Job Description Position Overview TriMed is seeking a Quality Engineer II to support the quality and compliance of our medical device products and manufacturing processes. In this mid-level role, you will independently lead investigations, support new product development, and partner cross-functionally to drive continuous improvement across the Quality Management System (QMS). This position is ideal for a hands-on quality engineer who thrives in a regulated medical device environment and enjoys balancing compliance, problem-solving, and cross-functional collaboration. What You’ll Do * Independently support and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, and internal procedures * Lead nonconformance investigations and CAPAs, ensuring timely and effective root cause resolution * Provide quality engineering support for new product development, including design reviews, design transfer, and V&V activities * Partner with Manufacturing and Operations to resolve production quality issues and drive process improvements * Review and approve Device History Records (DHRs), batch records, and inspection results * Lead Material Review Board (MRB) activities and disposition of nonconforming material * Support risk management activities in accordance with ISO 14971 * Participate in internal, supplier, and regulatory audits; support audit readiness and responses * Perform statistical analysis and trend quality data to identify improvement opportunities * Support validation activities (IQ/OQ/PQ) for processes, equipment, and software * Collaborate with Supplier Quality on supplier performance and corrective actions * Mentor junior quality staff and support continuous improvement initiatives Required Qualifications * Bachelor’s degree in Engineering or a related technical field (or equivalent experience) * 3–5 years of quality engineering experience in medical devices or regulated manufacturing * Working knowledge of FDA 21 CFR Part 820, ISO 13485, and ISO 14971 * Experience with CAPA, nonconformance investigations, and root cause analysis tools (5 Whys, Fishbone, FMEA) * Experience supporting design controls and/or manufacturing quality * Strong analytical and problem-solving skills * Ability to work independently and cross-functionally Preferred Qualifications * Experience with PPAP and APQP * Experience leading moderate NPI quality projects * Lean or Six Sigma training or certification * Experience supporting supplier quality activities * Advanced statistical analysis experience Travel & Work Environment * Approximately 20% travel * On-site role in Valencia, CA * Relocation assistance is not available for this position * Office environment Why Join TriMed At TriMed, you’ll work on meaningful medical device products in a collaborative, quality-driven environment. We value continuous improvement, cross-functional partnership, and professional growth. Benefits may include: * Medical, dental, and vision insurance * 401(k) with company match * Paid time off and holidays * Professional development opportunities TriMed, Inc. is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

Job DescriptionQuality Engineer I (QE I) Location: Valencia, CA (On-site, Monday–Friday) Department: Quality Employment Type: Full Time Position Overview TriMed is seeking a Quality Engineer I to support the quality and compliance of our medical device products and manufacturing processes. In this entry-level role, you will work under the guidance of senior quality engineers to support investigations, maintain the Quality Management System (QMS), and contribute to continuous improvement initiatives. This position is ideal for an early-career engineer who is eager to build hands-on experience in a regulated medical device environment. What You’ll Do * Support and maintain the QMS in compliance with FDA 21 CFR Part 820, ISO 13485, and internal procedures * Assist with nonconformance, deviation, and complaint investigations * Help draft and track CAPAs under senior guidance * Support new product development activities, including design reviews and V&V support * Provide quality engineering support to Manufacturing and Operations * Review and approve Device History Records (DHRs), batch records, and inspection results * Assist with Material Review Board (MRB) activities and disposition of nonconforming material * Support risk management activities in accordance with ISO 14971 * Participate in internal, supplier, and regulatory audits * Support validation activities (IQ/OQ/PQ) for processes, equipment, and software * Analyze quality data and support continuous improvement projects * Track and report quality metrics (KPIs) * Cross-train as backup support for document control, training management, complaints, and GUDID activities Required Qualifications * Bachelor’s degree in Engineering or related technical field (or equivalent experience) * 1–3 years of related experience (internships and co-ops may be considered) * Basic knowledge of FDA 21 CFR Part 820 and/or ISO 13485 * Strong analytical and problem-solving skills * Ability to work effectively in cross-functional teams * Strong written and verbal communication skills Preferred Qualifications * Medical device or other regulated manufacturing experience * Exposure to CAPA, NCR, or complaint handling processes * Familiarity with root cause tools (5 Whys, Fishbone, basic FMEA) * Working knowledge of SPC, MSA, or statistical methods * Experience with quality software (Minitab, JMP) * Basic knowledge of inspection techniques and document control Travel & Work Environment * Approximately 20% travel * On-site role in Valencia, CA * Office and manufacturing environment * Ability to occasionally lift up to 25 pounds with or without reasonable accommodation Why Join TriMed At TriMed, you’ll gain hands-on experience in a regulated medical device environment while working alongside experienced quality professionals. We value collaboration, continuous improvement, and professional development. Benefits may include: * Medical, dental, and vision insurance * 401(k) with company match * Paid time off and holidays * Professional development opportunities TriMed, Inc. is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

Job Description The Quality Engineer will evaluate and/or appraise supplier's manufacturing capabilities to baseline their processes for conformance to various documented commodity checklists, and/or QMS special processes. Establishes part quality evaluation plans from materials requests through material receipt (full life-cycle). Provides resolution and disposition of non-conformance materials to ensure adequate corrective action. • The Quality Engineer is highly supplier-focused, requiring excellent interpersonal and communication skills (oral and written) to manage supplier quality assurance responsibilities and ensure compliance across and at all levels of the organization on major programs from design through production stages., • Evaluation of manufacturing functions and processes to ensure Quality Standards are in place, • Evaluation of inspection and testing processes, mechanisms and equipment; and performs statistical analysis to assess the cost of and determine the responsibility for, products or materials that do not meet required standards and specifications., • Participate in QMS Audits for process deficiency and correction., • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements., • Interact in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality., • Involved in lean and six-sigma quality engineering methodologies., • Will have 'hands-on' knowledge and experience of mechanical (Machine Shop) components, assembly, subsystem and system level concepts., • Strong emphasis on RCCA and CAPA experience., • Minimum 3-5 years with LEAN Manufacturing Application experience., • 3-5 years' experience in areas of Quality Engineering such as: FMEA, SPC, RCCA, Process Control, Product Evaluation and Auditing, • 2-3 years' working knowledge and experience with ISO9100 and AS9100 QMS Processes, especially in Production and Quality Engineering, • 2-3 years' working knowledge and experience with Aircraft Parts and Material Conformity Inspections, • 3-5 years FAI experience with AS9102 (FAI) Protocol, • 3-5 years' knowledge and experience with inspection methods, techniques and protocols., • 3-5 years' experience in understanding and the application of Engineering Mechanical Processes, Standard Drawings Conventions, Interpreting Drawing Specifications (ANSI 14.5) and GD&T, • 3-5 years' experience in understanding and the application of Electronic Assembly Process and Inspection, Standard Conventions (IPC-610, J-Std-1000), Interpreting Schematic Diagrams and Specifications, • Airframe experience required, • AVMS electronic experience required, • Strong English verbal and written communication skills, • Reliable transportation must have current/active drivers' license, • Valid drivers license and auto insurance required, • In lieu of a Degree, 6+ years of hands-on experience as a Quality Engineering in an Aerospace Manufacturing Environment, • Bachelor's degree is preferred from an accredited college in technical discipline (e.g., Industrial Engineering, Mechanical Engineering, Quality Management), • Proficient with Microsoft Office Products (Excel, Outlook, PowerPoint, Word), • Compatible certifications or related college courses, • Team-minded, communicative, proactive, stress-resistant, assertive Benefits: • TRIGO AERO GROUP provides a 2% vacation bonus (2% of salary, excluding reimbursable expenses) for employees who meet the following conditions:, • One year of continuous employment, • Minimum of 1,400 hours worked in the year, • The hours calculation resets after every year, • 401k with employer match – available after 90 days of employment Company Overview TRIGO ADR Americas is the leader in the Aerospace & Defense Industry providing global Supplier Delivery Assurance, Supplier Development and Quality Management Services. Trigo provides a fully integrated service solution to optimize Supplier performance through an embedded “boots on the ground” business model to drive systemic changes that enhance Supplier Quality and Supplier Delivery performance. We work as an extension of our customers to build and maintain supplier and customer collaboration to ensure improved results and provide visibility throughout the supply chain. Trigo’s team of dedicated Delivery Assurance Specialists, Supplier Development Specialists, Supplier Quality Engineers and Program Managers support hundreds of Customers and are deployed to thousands of Suppliers worldwide focused on achieving On-Time and On-Quality Delivery results. TRIGO ADR Americas is an Equal Opportunity Employer, including disabled and veterans, and may require US Citizenship for employment on certain defense contracts subject to ITAR restrictions. All qualified candidates will receive consideration. Except where otherwise provided by law, selection will be made without regard to, and there will be no discrimination because of race, religion, color, national origin, sex, political affiliations, marital status, non-disqualifying physical or mental disability, age, sexual orientation, gender identity, genetic information, membership or non-membership in an employee organization, or on the basis of personal favoritism or other non-merit factors. Powered by JazzHR CSf4zcxUqT

Job Description JOB OVERVIEW: The VP of Commercial Operations reports to the CEO, has dotted line responsibility to the COO and is responsible for overseeing the daily operations of the company and ensuring efficiency, productivity, and quality across multiple departments. This role is responsible for end-to-end operational leadership of TriMed’s Valencia site, driving performance across inventory & materials management, customer service, contracts & pricing, IT & analytics, and operational quality/regulatory compliance. Accountable for aligning day-to-day operations with enterprise strategy, delivering on service level commitments, optimizing cost structure, and ensuring compliance with global medical device regulations. KEY RESPONSIBILITIES: • Provide executive leadership of day-to-day global operations for the extremities orthopedics business, spanning supply chain, customer service, contracts, IT, and regulatory compliance., • Drive operational excellence through standardized SOPs, robust KPIs, and cross-functional scorecards to optimize performance and scalability., • Build and cultivate a high-performance culture that attracts, develops, and retains top talent, with emphasis on accountability, collaboration, and continuous improvement., • Oversee global inventory, procurement, supply chain, and logistics to ensure availability of implants/instruments while optimizing COGS, asset utilization, and supplier partnerships., • Direct loaner set strategy, lifecycle management, and deployment to maximize salesforce effectiveness and customer satisfaction., • Champion customer-centric operations, including order-to-cash, pricing transparency, and voice-of-customer initiatives to strengthen distributor and healthcare provider relationships., • Govern enterprise contract and pricing management across IDNs, GPOs, and direct accounts, ensuring alignment with corporate strategy, compliance, and profitability., • Provide executive oversight of IT systems, ERP infrastructure, cybersecurity, and data analytics; advance automation and digital tools to enable data-driven decision making., • Partner with Finance to manage operational budgets, approve expenditures, and ensure financial discipline while enabling global revenue growth., • Collaborate with Quality and Regulatory Affairs to ensure compliance with FDA, MDSAP, ISO, OSHA, and global frameworks; lead inspection readiness and risk mitigation efforts., • Embed a culture of quality and operational excellence across processes including receiving/inspection, product compliance, and non-conforming material management., • Lead integrated business planning processes to align supply and demand, mitigate risks, and support global commercial competitiveness., • Lead strategic M&A due diligence efforts, ensuring seamless integration of operational and product functions., • Drive special projects and cross-functional initiatives as required to advance strategic priorities and business growth., • Performs other duties and supports special projects as needed SPECIFIC KNOWLEDGE & SKILLS: • Strong working knowledge of operations within a Medtech (preferably orthopedics) business., • Command of financial statements, • Experience managing RAQA compliance across multiple functions, • Experience managing Operations in a manufacturing business and working directly with multiple contract manufacturers GENERAL SKILLS & COMPETENCIES: • Outstanding management and leadership skills and ability to attract, retain, motivate, develop, mentor and coach team members for high performance, • Outstanding verbal and written communication skills and ability to resolve disputes effectively, • Outstanding presentation and public speaking skills, • Expert independent decision making, analysis and problem-solving skills, • Understand, interpret and act on financial information and external trends that contributes to business profitability, • Plan and manage complex and successful projects; understand available resources, develop timeline, budget and assign areas of responsibility, • Lead teams to achieve company goals and solve complex business issues in creative and effective ways, • Expert planning and organizational skills and techniques, • Communicate effectively with senior management and key stakeholders, • Excellent negotiating skills and ability to effectively manage internal and external relationships, • Ability to influence, build relationships, understand organizational complexities, manage conflict and navigate politics, • Broad professional and managerial skills with a full understanding of industry practices and company policies and procedures, • Lead and develop virtual teams, • Expert in multiple technical and business skills, • Strategic planning skills MINIMUM WORK EXPERIENCE: Typically 12 or more years of increasing responsibility and complexity in terms of any applicable professional experience; 5 or more years of management experience. PREFERRED EDUCATION: Typically a Bachelor's Degree or global equivalent in related discipline. Master's degree or global equivalent a plus. TRAVEL / PHYSICAL DEMANDS: Travel typically less than 10%. Office environment. No special physical demands required. SCOPE: Typically direct a large complex section of a department or a complex department with significant scope and financial and operational impact. Role may focus on executing large and very complex/complicated processes. Accountable for performance, results and staffing. Make recommendations for the objectives, policies and plans of the sub-function(s). Fully accountable for meeting the strategic, and operating objectives of the sub-function(s). Develop proposed budgets for approval and manage budget once approved. Operate with substantial latitude for un-reviewed action or decision. Often plays a role in high-level projects that have an impact on the company’s future direction. COMPLEXITY: Work on complex, numerous and unique issues where analysis of situations or data requires in-depth knowledge of the company and an evaluation of intangibles. Knowledge of all areas within sub-function(s) derived from experience in non-management and middle-management roles allowing for innovative concepts and promoting new ideas within the function. STRATEGY: Participate in establishing the strategic direction to ensure alignment with overall Company strategy and initiatives. Focus may be on the execution of a large and/or complex processes. Translate and guide team to implement strategy. SUPERVISION: Direct and control activities through several managers or senior professional level staff who have responsibility for the operation of the assigned area and/or process or system. INTERACTION: Regularly interact with executives and/or major customers/stakeholders. Ability to negotiate with customers or management and influence senior level leaders regarding matters of significance. Build personal networks to achieve mutually beneficial solutions. MANAGEMENT DUTIES: Can hire, terminate, or promote and is aware of higher-level functional issues and concerns. Makes decisions on salary increases, performance reviews, disciplinary actions, etc. PERFORMANCE REQUIREMENTS: Typically, to advance to a new job level, TSMs must demonstrate professional behavior and should consistently be at the high-end of meets expectations or consistently exceed expectations. TriMed, Inc. is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement a

The mission of the Quality Engineer is to provide leadership to project and/or production teams to ensure delivery of quality products. BS degree in Manufacturing or Mechanical Engineering with hands-on Quality manufacturing experience preferably in the aerospace industry; Master's degree (Mechanica

Read and interpret information from planning documents, drawings, tool orders, blueprints, sketches, specifications, engineering orders and quality assurance manuals to determine the methods and sequence of operations necessary to completely fabricate and machine all types and sizes of rocket engine

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We are seeking a Specialist, Manufacturing Engineer (Welding Engineer) to join our team in Canoga Park, CA, 2nd shift.This individual develops, implements and analyzes manufacturing engineering plans and projects and communicates them to internal and external customers.Defines and transfers manufact

This Jobot Job is hosted by: Colleen Gormley.Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume.Salary: $130,000 - $200,000 per year.If you are a skilled Trust & Estates Attorney with a passion for helping clients navigate the complexities of estate

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Differentiate between suppliers based on their technical process (Repeatability, Reliability) and business (Reliability, Rates, CSP, ISO compliant) capability.

Build Quality into all aspects of their work by maintaining compliance to all quality requirements. Quality Systems Test Software Engineer in the greater Santa Clarita Valley, CA or Waltham, MA areas. Responsible for developing, applying and maintaining quality standards for software products.

You will work closely with engineering, product, and operations to ensure that complex, interdependent workstreams stay on track and deliver high-quality results.

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This firm is the capital behind the homebuilding land deals you work on — a private equity platform that finances land acquisition, development, and homebuilding for public and private builders across the United States.It structures and deploys equity through lot option programs, land banking, and

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Key Responsibilities E xecute IQ, OQ, and PQ validation of complex systems and equipment Study time, motion, methods, and speed in maintenance and production operations to establish standard rates and improve efficiency Interpret engineering drawings, schematics, and formulas to determine quality an

Duties and Responsibilities include, but not limited to.Inspect and validate hardware to conform to AeroAntenna Technology s drawing or a given standard such as J-STD-001 or IPC-A-610 / IPC-A-600 / IPC6012.Review and maintain documentation.Receive into AMS ( Aeroantenna Management System).Successful

We are seeking a Specialist, Manufacturing Engineer (Welding Engineer) to join our team in Canoga Park, CA, 2nd shift.This individual develops, implements and analyzes manufacturing engineering plans and projects and communicates them to internal and external customers.Defines and transfers manufact

Comprehension and accurate execution of quality assurance methods and procedures. Complete inspection, work order, AS9102 1st Article and test records, reports, logs, rejection reports and inputting quality data into ERP database. Conduct inspections and tests of raw materials, in-process materials,

Construction Supervisor/Project Manager (PM) with Paul Davis.Manage reconstruction and renovations projects with homeowners and sub-contractors after traumatic events such as a fire or flood to repair damage to residential and commercial property.Celebrate completion of projects with a team of skill

Under minimal supervision, Project Manager III leads and ensures the successful delivery and management of complex, single or multiple projects within scope, quality, time and cost constraints that may be clearly defined or may require dynamic change management. Monitors project activities, ensuring

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This position has responsibility for gathering and analyzing agency data and assisting in the agency's quality control, quality assurance, and quality improvement efforts. Bachelor's degree in Quality Improvement/Quality Assurance, human services, psychology, or related social science field, or LVN