UNKNOWN

ADAPTED_NOW

At The Hospitals of Providence - Memorial Campus hospital, were seeking an innovative and experienced healthcare leader to drive excellence and inspire our team towards exceptional patient outcomes and operational success. Today, the Hospitals of Providence are comprised of our region's most trusted hospitals, each dedicated to meeting our families specific healthcare needs.

<h3>Overview</h3> 
﻿Are you a results-driven leader ready to make a meaningful impact to patients, caregivers, and your community? At The Hospitals of Providence - Memorial Campus hospital, were seeking an innovative and experienced healthcare leader to drive excellence and inspire our team towards exceptional patient outcomes and operational success. At The Hospitals of Providence - Memorial Campus, we understand that our greatest asset is our dedicated team of professionals. That’s why we offer more than a job – we provide a comprehensive benefit package that prioritizes your health, professional development, and work-life balance. The available plans and programs include:<ul><li>Medical, dental, vision, and life insurance</li><li>401(k) retirement savings plan with employer match</li><li>Generous paid time off</li><li>Career development and continuing education opportunities</li><li>Health savings accounts, healthcare & dependent flexible spending accounts</li><li>Employee Assistance program, Employee discount program</li><li>Voluntary benefits include pet insurance, legal insurance, accident and critical illness insurance, long term care, elder & childcare, auto & home insurance</li></ul>Note: Eligibility for benefits may vary by location and is determined by employment status<h3>Job Summary</h3>Full Time, DaysDirects and provides leadership over operations. Has ability to hire, fire and discipline. Typically reporting to hospital COO.<h3>Responsibilities</h3>Ensures personnel maintain, operate, test, inspect and perform preventative maintenance checks and repair medical electronic/ hydraulic, pneumatic equipment. Operates patient safety equipment and understands recorded data. Processes all equipment repairs and preventative maintenance checks on all equipment. Submits reports, purchase orders and records. Schedules work assignments. <h3>Qualifications</h3>Education Required:  Must have an Associate degree in Biomed/related field or equivalent military training certificate.  Preferred:  Bachelor's degree in Biomed or related field.Experience Required:  10 years in Biomedical Department. 5 years in supervision.<h3>Organization Description</h3>The Hospitals of Providence have faithfully been serving our community since 1902. Generations of families have chosen our hospitals to be a steward of health in the El Paso community. Our five hospitals include a childrens hospital committed to providing the care patients need, when they need it. Today, the Hospitals of Providence are comprised of our region's most trusted hospitals, each dedicated to meeting our families specific healthcare needs. Join our team!
Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status.
Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. 
Tenet participates in the E-Verify program. Follow the link below for additional information. 
E-Verify: <a href="http://www.uscis.gov/e-verify" rel="nofollow noopener noreferrer" target="_blank">http://www.uscis.gov/e-verify</a> 
The employment practices of Tenet Healthcare and its companies comply with all applicable laws and regulations.

2603008805 Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.

The Hospitals of Providence - Memorial Campus

Director of Biomed Engineering

Biomedical Engineering

Biomedicine

Equipment Maintenance/Repair

Flexible Spending Accounts

Healthcare

Hospital

Hydraulic Engineering

Leadership

Life Insurance

Maintenance Services

Military

Patient Care

Patient Safety

Preventative Maintenance

Purchase Orders

Regulations

Safety Equipment

Testing

Vision Plan

Tenet Healthcare Monster

CONTRACTOR

FEED

Our Total Rewards program which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components is designed to support the varying needs of our diverse and global associates. The Product Development Engineer executes specific and general assignments / projects that provide innovative, functional and cost-effective solutions to support product development and commercialization in a team-based environment.

Product Development, Engineer 1 Be part of something bigger! Shift 8-5PM Interviews in person Is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. The Product Development Engineer executes specific and general assignments / projects that provide innovative, functional and cost-effective solutions to support product development and commercialization in a team-based environment. The PD Engineer is responsible for the tactical execution of product development deliverables while adhering to established quality, design control processes and good engineering practices. Responsibilities: Supports the development of new products by applying engineering fundamentals and concepts to advance product development deliverables within the functional area. Support installation and qualification of R&D equipment. Perform data analysis and write technical reports based on product development activities. Support purchasing process of materials, equipment and testing consumables. Develop and validate test methods for raw materials and in-process inspections (i.e., Gage R&R). Ensure compliance with Design Control process requirements throughout the product lifecycle Support Design Control process activities such as the creation and maintenance of Design History Files (DHF) and risk management (DFMEA) documentation. Support the development of DMR documentation such as raw material specifications, component specifications, test methods, manufacturing instructions, etc. Conduct engineering testing, including performance, reliability, and usability assessments. Participate in design reviews, root cause analysis, and failure investigations. Assist in technology transfer and process validation activities for new product introductions Ensure compliance with quality policies, procedures and practices as well as with all local, state, federal and safety regulations, policies and procedures. Required Competencies/Skills: Education: BS degree in Engineering is required (Mechanical or Biomedical preferred) Able to adapt to shifting priorities, organize and self-manage the execution of assigned work in a fast-paced environment. Strong problem-solving skills relevant for the role. Comfortable with ambiguity and able to make progress in the face of uncertainty. Able to proactively anticipate challenges and technical risks for assigned work and identify a path to overcome obstacles in a compliant manner. Must possess proficient verbal and written communication skills. Displays effective interpersonal skills to assist the advancement and success of the cross-functional team. Proficient with the application of statistical principles to analysis of engineering results (capability analysis, normality, acceptance sampling, DoE). Additional required skills: Acquaintance with FDA regulations for medical device, drug product and combination product guidance is a plus. Adept in root cause analysis techniques (i.e., 5 whys, Ishikawa, etc) Acquaintance with the use of computer assisted statistical tools (minitab, excel) Displays personal leadership and bias for action to drive for results. Experience 1-2 years of product engineering and/or pharmaceutical development experience with an emphasis on moving from pilot to commercial scale production within a pharmaceutical environment. 1-2 years of experience working in an FDA regulated environment (21CFR211, 21CFR820, ISO13485). Experience with statistical techniques and technical writing (beyond templated IQ/OQ/PQ documents). Process excellence training or certification would be highly desired (ex. LSS-Green belt). Experience working in a fast-paced and cross-functional environment. Consistent with Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Primary Location: North America- United States-El Paso, TX Job Function: R&D / New Product Development Why join us A career at means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their lifes purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components is designed to support the varying needs of our diverse and global associates. Is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status.

Apidel Technologies

Engr 1, Product Development

Analysis Skills

Biotech and Pharmaceutical

Code of Federal Regulations

Communication Skills

Cross-Functional

Data Analysis

Design Failure Mode and Effects Analysis (DFMEA)

Documentation

Drug Development

Drug Products

FDA (Food and Drug Administration)

FDA Requirements

Federal Laws and Regulations

GEP (Good Engineering Practices)

Genetics

ISO (International Organization for Standardization)

International Health

Interpersonal Skills

Maintain Compliance

Manufacturing Methods

Materials Testing

Medical Diagnosis

Medical Equipment

Minitab

Performance Testing

Presentation/Verbal Skills

Process Validation

Product Development

Product Engineering

Product Lifecycle

Product Support

Product/Service Launch

Purchasing/Procurement

Quality Assurance Methodology

Quality Control

Reliability Analysis

Reporting Skills

Research & Development (R&D)

Risk Management

Root Cause Analysis

State Laws and Regulations

Statistics

Technical Writing

Test Plan/Schedule

Usability Engineering

Writing Skills

partner Conrep

Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates. The Product Development Engineer executes specific and general assignments / projects that provide innovative, functional and cost-effective solutions to support product development and commercialization in a team-based environment.

Client is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. The Product Development Engineer executes specific and general assignments / projects that provide innovative, functional and cost-effective solutions to support product development and commercialization in a team-based environment. The PD Engineer is responsible for the tactical execution of product development deliverables while adhering to established quality, design control processes and good engineering practices. Responsibilities:<ul><li> Supports the development of new products by applying engineering fundamentals and concepts to advance product development deliverables within the functional area.</li></ul> · Support installation and qualification of R&D equipment. · Perform data analysis and write technical reports based on product development activities. · Support purchasing process of materials, equipment and testing consumables. · Develop and validate test methods for raw materials and in-process inspections (i.e., Gage R&R). · Ensure compliance with Design Control process requirements throughout the product lifecycle <ul><li> Support Design Control process activities such as the creation and maintenance of Design History Files (DHF) and risk management (DFMEA) documentation.</li><li> Support the development of DMR documentation such as raw material specifications, component specifications, test methods, manufacturing instructions, etc.</li><li> Conduct engineering testing, including performance, reliability, and usability assessments.</li><li> Participate in design reviews, root cause analysis, and failure investigations.</li><li> Assist in technology transfer and process validation activities for new product introductions</li></ul> · Ensure compliance with Client quality policies, procedures and practices as well as with all local, state, federal and Client safety regulations, policies and procedures. Required Competencies/Skills:<ul><li> Education: BS degree in Engineering is required (Mechanical or Biomedical preferred)</li></ul> · Able to adapt to shifting priorities, organize and self-manage the execution of assigned work in a fast-paced environment.<ul><li> Strong problem-solving skills relevant for the role.</li></ul> · Comfortable with ambiguity and able to make progress in the face of uncertainty.<ul><li> Able to proactively anticipate challenges and technical risks for assigned work and identify a path to overcome obstacles in a compliant manner.</li></ul><ul><li> Must possess proficient verbal and written communication skills.</li><li> Displays effective interpersonal skills to assist the advancement and success of the cross-functional team.</li></ul> · Proficient with the application of statistical principles to analysis of engineering results (capability analysis, normality, acceptance sampling, DoE). Additional required skills:<ul><li> Acquaintance with FDA regulations for medical device, drug product and combination product guidance is a plus.</li><li> Adept in root cause analysis techniques (i.e., 5 why's, Ishikawa, etc)</li><li> Acquaintance with the use of computer assisted statistical tools (minitab, excel)</li></ul> · Displays personal leadership and bias for action to drive for results. Experience<ul><li> 1-2 years of product engineering and/or pharmaceutical development experience with an emphasis on moving from pilot to commercial scale production within a pharmaceutical environment.</li></ul> · 1-2 years of experience working in an FDA regulated environment (21CFR211, 21CFR820, ISO13485).<ul><li> Experience with statistical techniques and technical writing (beyond templated IQ/OQ/PQ documents).</li><li> Process excellence training or certification would be highly desired (ex. LSS-Green belt).</li><li> Experience working in a fast-paced and cross-functional environment.</li></ul> Consistent with Client's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. PRIMARY LOCATION: North America- United States-El Paso, TX JOB FUNCTION: R&D / New Product Development Why join us? A career at Client means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our associates can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates. To learn more about Client visit <a href="https://jobs.Client.com/" rel="nofollow"> https://jobs.Client.com/</a> "Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status.”

TechDigital Corporation

TechDigital Corporation Jobs

Biomedical Engineering jobs in El Paso, TX on your radar? Find the best of them right here on Monster.

The Best Biomedical Engineering Jobs in El Paso, TX | Monster

Biomedical Engineering Jobs in El Paso, TX

Jobs

Resume Resources

Get noticed by top employers!

Biomedical Engineering Jobs in El Paso, TX

Jobs

Director of Biomed EngineeringThe Hospitals of Providence - Memorial Campus

Engr 1, Product DevelopmentApidel Technologies

Engr 1, Product DevelopmentTechDigital Corporation

Resume Resources