UNKNOWN

ADAPTED_NOW

We're hiring a full-time entry-level Biomedical Engineer to join our Virtual Surgical Planning department, where you'll prepare planning files by analyzing medical imaging, simulating surgical procedures, and developing cephalometric analyses. Our Employee Resource Group program, Employee Recognition program, and 3D Gives Back program, are just a few examples of how you will be empowered to build connections, celebrate wins, and make a meaningful impact.

YEAR

What We Are Looking For   We're hiring a full-time entry-level Biomedical Engineer to join our Virtual Surgical Planning department, where you'll prepare planning files by analyzing medical imaging, simulating surgical procedures, and developing cephalometric analyses. You'll also ensure product quality through inspection of 3D printed patient-specific medical devices, modification of surgical splints, and meticulous data organization. Join our team to apply cutting-edge biomedical engineering skills while directly impacting surgical outcomes and patient care!   Onsite   This role has an onsite work schedule requiring the person to be in the onsite location 5 days a week.   What's in it for You!   - Competitive Pay: $65,000 - $75,000 per year. Our employees are the best part of our company. We want you to feel valued, appreciated, and included. Because of this, we make sure your hard work is recognized. - Paid Leave (US ONLY): Enjoy time away from work with Company paid holidays and a flexible working schedule through our paid time off (PTO) policy. Yep, you read that correctly. We are a Company that values you and makes sure you take time for yourself. - 401(k): Prepare for a secure retirement with our 401k plan, which includes an employer matching contribution. - Comprehensive Health & Wellness Plans: We want to be here for our employees throughout all stages of life, which is why we offer a wide range of resources, information, and support during your career with us. - Global Team: With our state-of-the-art corporate headquarters in Rock Hill, South Carolina, our global team has a presence across more than 15 countries worldwide. Experience a workplace comprised of talented individuals who are passionate about serving our customers and each other. - Innovative Culture: Innovation is at the heart of what we do! Since our founding in 1986 by Chuck Hull, the inventor of 3D printing, we have continuously pushed the boundaries of what is possible with additive manufacturing. When you join 3D, you will have the opportunity to work with cutting edge technology in an innovative and collaborative culture - Talent Development: At 3D Systems, we invest in talent programs to support employees with opportunities to grow, contribute, develop, and thrive in their careers. - Connection & Engagement Opportunities: We strive to cultivate an environment where our diverse global workforce can connect and thrive. Our Employee Resource Group program, Employee Recognition program, and 3D Gives Back program, are just a few examples of how you will be empowered to build connections, celebrate wins, and make a meaningful impact.   What You Will Do   - Interface directly with healthcare professionals, staff, and sales representatives to perform surgical planning via phone, emails and web meetings. - Use CAD software to manipulate 3D files and combine multiple datasets for surgical planning. - Manage multiple priorities and communicate closely with a multidisciplinary team. - Maintain detailed records of each case in accordance with the company's Quality Management System. - View patient CT and MRI studies in DICOM format and identify anatomies of interest. - Perform inspection of 3D printed surgical guides for quality and clinical effectiveness. - Use hand tools to buff, clean, or modify the surgical guides as needed.   ## Qualifications   What You Will Bring   - BS degree in Biomedical, Mechanical or other relevant technical field required. - Experience: Transferable skills from projects, internships, academic work or previous work relevant to the role. - Experience collaborating or interacting with medical professionals - Ability to build and maintain relationships with key customers   Applications accepted online through July 18, 2025   #LI-MP1   3D Systems s an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, ethnicity, religion, sex, age, sexual orientation, genetic information, marital status, gender identity or national origin or because he or she is an individual with a disability or a disable veteran, Armed Forces service medal veteran (referred to collectively as "protected veterans"). The Company also provides applicants with equal employment opportunities without regard to pregnancy, childbirth, medical needs arising from pregnancy or childbirth, and related medical conditions including, but not limited to, lactation. Apply URL - https://ars2.equest.com/?response_id=d5dc11d2a870d18c65c4fa0868b76330

Space Systems Integr

Senior Space Vehicle Test Engineer

KPMG

OTHER

FEED

Manage customer relations: respond to RFQs, prepare and review new PO quotes (costing, lead‑times, capacity impact), negotiate delivery schedules and terms with sales/account managers, and host or conduct customer site visits and plant tours to support sales, qualification, and audits. Accountable for meeting quality, regulatory, cost, delivery, and safety targets while driving continuous improvement, robust training programs, quality controls, customer relations, and people development.

POSITION PURPOSE & SUMMARYExperienced operations leader responsible for safe, compliant, timely production of precision machine components. Accountable for meeting quality, regulatory, cost, delivery, and safety targets while driving continuous improvement, robust training programs, quality controls, customer relations, and people development.ESSENTIAL FUNCTIONS<ul><li style="text-align:justify">Managing and leading medical device manufacturing operations.</li><li style="text-align:justify">Lead day‑to‑day plant operations across production, packaging, sterilization (if applicable), maintenance, and facilities.</li><li style="text-align:justify">Maintain and improve product quality, yield, and on‑time delivery metrics. Investigate and resolve nonconformances, CAPAs, NCRs, and recalls when needed.</li><li style="text-align:justify">Design, implement, and sustain comprehensive training programs for production, quality, maintenance, and supervisory staff (onboarding, GMP, QMS, safety, SOPs, competency assessments). Track training effectiveness and ensure competency records are maintained.</li><li style="text-align:justify">Establish, monitor, and enforce quality controls across manufacturing processes, including in‑process inspections, lot release criteria, SPC, first‑article inspections, and final product verification. Ensure effective sampling plans, test methods, and documentation.</li><li style="text-align:justify">Oversee production planning, capacity management, and scheduling to meet customer demand and inventory targets.</li><li style="text-align:justify">Manage customer relations: respond to RFQs, prepare and review new PO quotes (costing, lead‑times, capacity impact), negotiate delivery schedules and terms with sales/account managers, and host or conduct customer site visits and plant tours to support sales, qualification, and audits. Coordinate technical responses and ensure commitments are feasible and validated.</li><li style="text-align:justify">Implement and sustain lean manufacturing, continuous improvement, and cost‑reduction initiatives (e.g., 5S, Kaizen, Six Sigma).</li><li style="text-align:justify">Manage plant budget, P&L drivers, cost control, and capital projects.</li><li style="text-align:justify">Ensure workplace health & safety, environmental compliance, and emergency preparedness.</li><li style="text-align:justify">Collaborate with R&D, Quality, Regulatory Affairs, Supply Chain, and Sales on new product introductions, transfers, validations, change controls, and contract requirements.</li><li style="text-align:justify">Oversee equipment validation, preventive maintenance, calibration programs, and supplier/contractor performance.</li><li style="text-align:justify">Maintain accurate documentation, manufacturing records, training records, and metrics reporting to senior leadership.</li><li style="text-align:justify">Drive continuous improvement of the QMS and training systems; participate in internal and external audits and implement corrective actions.</li></ul><h1>PROFESSIONAL REQUIREMENTS – KNOWLEDGE, SKILLS & ABILITIES:</h1>Skills Required<ul><li style="text-align:justify;line-height:90%;background:#ffffff">Hands‑on experience with CNC lathe and milling machines (turning, milling centers).</li><li style="text-align:justify;line-height:90%;background:#ffffff">CNC programming skills (G‑code, conversational, and CAM software such as Mastercam, Fusion 360, or Autodesk).</li><li style="text-align:justify;line-height:90%;background:#ffffff">Tooling selection and setup: toolholders, inserts, collets, endmills, drills, live tooling, and fixture design/placement.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Machine setup and changeover: offsets, work holding, speeds/feeds optimization, probe setup, and first‑piece approval.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Precision dimensional inspection: use of CMM, calipers, micrometers, height gauges, bore gauges, optical comparators, and surface finish measurement.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Blueprint reading and tolerance interpretation, GD&T competency.</li><li style="text-align:justify;line-height:90%;background:#ffffff">SPC and in‑process inspection techniques; root‑cause analysis for dimensional nonconformances.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Preventive maintenance and basic troubleshooting of CNC equipment.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Strong attention to detail, quality focus, and ability to train/mentor operators on machining and inspection best practices.</li><li style="text-align:justify;line-height:90%;background:#ffffff">Preferred: certification or demonstrated experience in CNC machining, metrology, or precision manufacturing.</li></ul>Required Qualifications<ul><li style="text-align:justify;line-height:90%">Bachelor's degree in engineering, Manufacturing, Biomedical Engineering, Life Sciences, or related field.</li></ul>Or<ul><li>8+ years manufacturing experience with at least 3–5 years in a plant leadership role; medical device experience strongly preferred.</li><li>Demonstrated success in operational excellence, process validation, and continuous improvement programs.</li><li>Proven ability to design and manage training programs and maintain training records/competency matrixes.</li><li>Experience interacting with customers for quoting, contract review, site visits, and technical negotiations.</li><li>Proven ability to manage budgets, forecasting, and capital projects.</li><li>Excellent leadership, communication, customer‑facing, problem‑solving, and cross‑functional collaboration skills.</li></ul>License, Registration, and/or Certification Requiredþ Valid Driver's License PHYSICAL REQUIREMENTS, WORKING CONDITIONS & ENVIRONMENTAL FACTORS<ul><li>Plant environment with PPE requirements; ability to walk production floors and inspect equipment.</li><li>May require overtime, shift coverage, and occasional travel to suppliers, customers, or other sites.</li></ul>COMPENSATION & BENEFITS<ul><li>Competitive salary commensurate with experience plus performance bonus. Comprehensive benefits package (health, retirement, PTO, etc.).</li></ul>Equal OpportunityGMI is an equal opportunity employer and values diversity. Reasonable accommodation is available for qualified applicants.  Job Posted by ApplicantPro

Garden of the Gods Resort and Club

Medical Device - Plant Manager

Best Practices

Biology

Biomedical Engineering

Blueprints

Budget Management

CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing)

CNC (Computerized Numerical Control) Systems

CNC Lathe

CNC Milling Machine

Calibration

Capability Maturity Model (CMM)

Capacity Management

Capital Project

Change Control

Communication Skills

Computer Programming

Continuous Improvement

Contract Requirements

Contract Review

Corrective Action

Cost Control

Customer Relations

Detail Oriented

Documentation

Driver's License

Environmental Compliance

Equipment Validation

External Audit

Facilities and Maintenance

Forecasting

GMP (Good Manufacturing Practices)

Geometric Dimensioning and Tolerancing

Identify Issues

Internal Audit

Leadership

Lean Manufacturing

Machine Tool

Machining

Manufacturing

Manufacturing Operations

Manufacturing/Industrial Processes

Medical Equipment

Mentoring

Metrics

Metrology

Negotiation Skills

Onboarding

Operations Processes

Physical Demands

Plant Management

Preventative Maintenance

Problem Solving Skills

Process Improvement

Process Validation

Product/Service Launch

Production Control

Production Machining

Production Planning

Profit & Loss

Project/Program Management

Quality Assurance Methodology

Quality Management

Quality Monitoring

Record Keeping

Regulations

Request for Proposals (RFP)

Research & Development (R&D)

Root Cause Analysis

Safety Compliance

Safety/Work Safety

Sales

Sales Management

Sales Qualification

Sales Support

Six Sigma

Standard Operating Procedures (SOP)

Sterilization

Supply Chain

Team Player

Technical Leadership

Time Management

Training Program

Training Program Development

Training/Teaching

Turning Center

Vendor/Supplier Evaluation

Vision Comparator

Willing to Travel

Talent Acquisition

Bachelor's degree or foreign equivalent in Biomedical Engineering, Mechanical Engineering, or related field, and one (1) year of engineering experience in the medical device industry or related. Research and develop the design and component selection of mechanical sub systems with the goal of producing products that are simpler to manufacture at scale.

Hologic, Inc. has an opening in Louisville, CO. Details are as shown below: JOB TITLE: Sr. Product Development Engineer [SPDEAB525] WORKSITE: 331 S. 104 Street. Suite 200. Louisville, CO 80027. *No telecommuting allowed within the U.S. Up to 15% travel to production sites and suppliers. WAGE RANGE: $95,493 - $146,900 annually JOB DESCRIPTION Support the validation, design, development, verification, and launch of biomedical products and electromechanical systems. Research and develop the design and component selection of mechanical sub systems with the goal of producing products that are simpler to manufacture at scale. Contribute towards the next generation of Hologic surgical products including, MyoSure®, NovaSure®, OmniLok®, CoolSeal, Acessa and Fluent®. Design, fabricate, and test prototypes. Document test protocols and results. Provide R&D laboratory support, testing and instrumentation. Design engineering studies. Perform tests, collect data, and interpret results. Own defined components or sub-assemblies of assigned design projects. Leverage CAD for drawings and design. Prepare and maintain compliant engineering documentation. Identify potential suppliers to solve needs for assigned projects. Conduct design review meetings, seeking to freeze components and sub system level assemblies. Draft design verification and validation protocols and reports. Support technical writing of 510K submissions to the FDA and prepare required technical documentation to present information to the FDA. Up to 15% travel to production sites and suppliers. MINIMUM REQUIREMENTS Bachelor's degree or foreign equivalent in Biomedical Engineering, Mechanical Engineering, or related field, and one (1) year of engineering experience in the medical device industry or related. SKILLS REQUIREMENTS Experience must include one (1) year in each of the following: 1) Machined components design, and molded injected parts design; 2) Using design controls to verify and validate designs, including test development and execution, requirements writing, usability, and knowledge of human factors; 3) CAD (SolidWorks); 4) Rapid prototyping for both 3D printing and conventional machine shops; 5) Statistical methods to design experiments and demonstrate design feasibility of solutions; 6) International standards for packaging medical devices and determining medical device biological compatibility (ISO 10993); 7) Performing tolerance stack-up analyses of medium to large mechanical assemblies; and 8) Risk management and failure mode analysis (FMEA). Background checks may be required. APPLICANT INSTRUCTIONS: To apply, email resume to Talent.Operations@hologic.com. Must reference job title and job code.

Cimarron Software Se

IT Material Life Cycle Lead

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Senior Space Vehicle Test EngineerSpace Systems Integr

Medical Device - Plant ManagerGarden of the Gods Resort and Club

IT Material Life Cycle LeadCimarron Software Se

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