6 Medical Technology jobs in Dallas

About Rotech Rotech Healthcare Inc. is a national leader in providing ventilators, oxygen, sleep apnea treatment, wound care solutions, diabetic solutions and home medical equipment. We help patients lead a more comfortable and productive life by keeping them engaged in their care and empowering them to manage their health and treatment at home. Rotech provides high quality medical products, services and outstanding customer care through hundreds of locations across 45 states. For additional information, visit our company homepage Rotech.com Overview and Responsibilities Job Summary We are seeking a dedicated Patient Service Technician to join our team. In this position, you are responsible for delivery and set-up of equipment at the delivery address. Educates the patient and/or caregiver on the safe use and maintenance of the delivered item. Employee will be expected to be a part of an on call rotation. Essential Job Duties and Responsibilities (Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.) Adheres to company policies and procedures in regards to using personnel protective safety equipment and services Assists in resolving customer equipment problems under emergency conditions Assists with implementation of quality improvement programs to meet company and JCAHO standards Assumes on-call responsibilities during non-business hours in accordance with company policy Communicates to supervisor any vehicle problems or conditions which would otherwise compromise the vehicle's safe operations Completes shipping papers when transporting hazardous materials in accordance to Rotech policy and procedures Completes written patient visit reports following setup and follow-up visits per company policy Delivers and educates patients on the safe use and maintenance of respiratory and HME equipment in the home or office setting Develops and maintains working knowledge of current HME products and services offered by the company; and all applicable governmental regulations Develops basic reimbursement knowledge, completely documents all information Develops technical knowledge, as appropriate, of the HME or respiratory products Maintains assigned company vehicle in a clean and safe working condition Maintains delivery activity database Maintains home oxygen systems in patients' homes per company policy Manages territory to reach service goals and delivers equipment and oxygen as required in accordance with industry standards and applicable federal, state and local governmental regulations Prepares and maintains written company records to include invoices, work orders, manifests and logs Processes all orders and required paperwork in a timely and accurate manner Reports equipment hazards and/or product incidents as required in accordance with company policies Ability to work cooperatively with others Deal politely with patients and referral sources Manage several tasks at once Performs other duties as assigned Travel Travel via company vehicle required to patient's homes for set-ups and reoccurring delivery Qualifications Employment is contingent on Background investigation (company-wide) Drug screen (when applicable for the position) Valid driver's license in state of residence with a clean driving record (when applicable for the position) Required Education and/or Experience High school diploma or GED equivalent, required Preferred Education and/or Experience Experience with medical equipment, preferred One year of related work experience, preferred Medical terminology, preferred Skills and Competencies Accurately perform simple mathematical calculations Effectively communicate in English; both oral and written Interpret a variety of communications (verbal, non-verbal, written, listening and visual) Maintain confidentiality, discretion and caution when handling sensitive information Multi-task along with attention to detail Self-motivation, organized, time-management and deductive problem solving skills Work independently and as part of a team Machines, Equipment and Technical Abilities Email transmission and communication Internet navigation and research Microsoft applications; Outlook, Word and Excel Office equipment; fax machine, copier, printer, phone and computer and/or tablet Mechanically inclined for the repair and troubleshooting of equipment Successfully demonstrates loading, unloading and proper tie down procedures as per company policy of transported cargo Understands use of all applicable home respiratory equipment and supplies Physical Demands Lift and carry office equipment at times Requires sitting, walking, standing, talking and listening Requires close vision to small print on computer and/or tablet and paperwork Requires lifting (minimum of 65 pounds) and transporting of patient equipment Requires contact with patients and equipment with potential exposure to contagious pathogens Requires driving a company vehicle for the majority of the workday Required to comply with Rotech Respiratory Protection & N95 Mask Fit Testing Policy Medical Evaluation and Fit Testing Compliance in a timely manner Annual Recertification Keep face clean-shaven to ensure N95 Mask face-seal protection per OSHA guidelines Rotech Information Benefits Generous paid time Off and paid holidays Overtime pay for non-exempt hourly positions based on business needs Commission for

Job Title

Senior Project Manager - Medical Equipment

Job Type

Full-time

Location

Dallas, TX 75201 US (Primary)

Education

Bachelor's Degree

Category

Medical Equipment Planning

Job Description

Hoefer Welker is seeking a qualified Senior Medical Equipment Planner/Project Manager. Candidate must have minimum 15 years of experience developing new medical equipment plans for new or renovated healthcare construction projects, in-depth knowledge of medical equipment technologies and coordinating with architectural design teams.

Roles and Responsibilities

• Based on experience, leads and manages larger/complex projects for medical equipment planning or procurement services, and multiple team members.
• Works independently as a primary liaison for the client, architect or project team and utilizes project managers and coordinators to deliver work.
• Participates in project design or procurement meetings and is responsible for developing, managing and coordinating project deliverables.
• Actively manages project team communications, documentation and awareness of project scope of services, workplans and managing hours against fee.
• Responsible for managing project financials and A/R collections for assigned projects.
• Serves as a leader and mentor for project managers and coordinators.
• Assists with business development and participates in client presentations.

Job Requirements

Bachelor's Degree in Architecture or equivalent in education or experience.

Certification/Registration:

• PMP certification a plus

Qualifications:

Candidate must have minimum 15 years of experience developing new medical equipment plans for new or renovated healthcare construction projects. Plus 5-10 years of experience in architectural practice as a project architect on healthcare projects is required. Must have full working knowledge of Microsoft Office (Outlook, Word, Excel, PowerPoint); REVIT experience; Deltek Vision experience; Requirements for this position include detail driven habits, ability to maintain focus in a fast paced environment. Must have excellent organizational and multi-tasking skills, ability to work effectively in a team atmosphere and be deadline oriented. Handles confidential and proprietary information. Ability to identify challenges and demonstrate independent judgment in decision making. Takes initiative and demonstrates resourcefulness.

Physical Demands:

While performing the responsibilities of this job, the employee is required to talk and hear. The employee is often required to sit and use their hands and fingers, to handle or feel and to manipulate a keyboard or computer mouse. The employee is occasionally required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl. Vision abilities required for this job include close vision.

To perform this job successfully, an individual must be detail oriented and able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Equal Opportunity Employer/Veterans/Disabled

Senior Project Manager - Medical Equipment - (CTSPM - 6.25TX)

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Job Details

• Job Title: Senior Project Manager - Medical Equipment
• Job Type: Full-time
• Location: (Location not specified)
• Education: Bachelor's Degree
• Category: Medical Equipment Planning

Job Description

Hoefer Welker is seeking a qualified Senior Medical Equipment Planner/Project Manager. The candidate must have a minimum of 15 years of experience developing medical equipment plans for healthcare construction projects, with in-depth knowledge of medical equipment technologies and experience coordinating with architectural design teams.

Roles and Responsibilities

• Lead and manage complex projects for medical equipment planning or procurement, overseeing multiple team members.
• Serve as the primary liaison for clients, architects, and project teams, utilizing project managers and coordinators to deliver results.
• Participate in project design and procurement meetings, developing and managing project deliverables.
• Manage project communications, documentation, scope, workplans, and hours against fee.
• Handle project financials and accounts receivable collections.
• Mentor and lead project managers and coordinators.
• Support business development and client presentations.

Job Requirements

• Bachelors Degree in Architecture or equivalent experience.
• At least 15 years of experience in medical equipment planning for healthcare projects.
• 5-10 years of experience as a project architect in healthcare architecture.
• Proficiency in Microsoft Office, REVIT, Deltek Vision.
• Detail-oriented, organized, and capable of multi-tasking in a fast-paced environment.
• Excellent teamwork, communication, and deadline management skills.
• Ability to handle confidential information and demonstrate independent judgment.

Physical Demands

Must be able to talk, hear, sit, use hands, handle objects, and occasionally stand, walk, reach, climb, or kneel. Vision abilities include close vision. Reasonable accommodations will be provided for individuals with disabilities.

This job is active and recruiting; it is not expired.

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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
**Working at Abbott**
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
+ Career development with an international company where you can grow the career you dream of.
+ Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
+ An excellent retirement savings plan with high employer contribution
+ Tuition reimbursement, the Freedom 2 Save ( student debt program and FreeU ( education benefit - an affordable and convenient path to getting a bachelor's degree.
+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
+ A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it's glucose monitoring system, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
**The Opportunity**
Our location in Plano, TX, Austin, TX, Santa Clara, CA, Sylmar CA or Maple Grove, MN currently has an opportunity for a **Clinical Evaluation - Senior Project Manager** . This new team member will combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with MEDDEV 2.7/1 Rev 4, MDD, AIMDD, MDCG Guidance documents, and EU MDR 2017/745. This role will support the Neuromodulation product lines.
**What You'll Work On**
+ Manage, provide guidance, and oversight of CER Medical Writers' development of Clinical Evaluation Reports and associated documents; set deliverable and project timelines and ensure timelines are met.
+ Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing, Library Services, Quality Engineering, Post-market Surveillance Group, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
+ Review, edit, and write portions, as needed, of Clinical Evaluation Reports and associated documents.
+ Participate in and/or lead the development of regulatory responses for Notified Body questions upon review of submissions.
+ Provide strategic guidance on regulatory requirements, pertaining to clinical data and clinical evaluations, to new product development teams and sustaining teams.
+ Compliance with applicable corporate and divisional policies and procedures.
+ Participate in and support internal and external audits and responses to audit findings as appropriate, in root cause analysis, preventive or corrective actions, effectiveness monitoring, and other quality metrics.
+ Develop and update new policies, as appropriate, for processes and procedures relating to the clinical evaluation process, and train key personnel on them.
+ Function independently as a decision-maker on CER-related regulatory issues.
**Required Qualifications**
+ Bachelor's Degree
+ Minimum 2 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
+ Minimum 3 years of experience in a regulated industry (e.g., medical products, nutritionals). Note: Higher education may compensate for years of experience.
+ Principles and requirements of applicable product laws
+ Ethical guidelines of the regulatory profession, clinical research and regulatory process
+ Create and manage project plans and timelines
+ Think analytically, pay strong attention to detail, organize and track complex information
+ Exercise judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results
+ Follow scientific arguments, identify regulatory scientific data needs and solve regulatory issues.
**Preferred** **Qualifications**
+ Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields.
+ Advanced degree
+ Scientific/research background; training and degree in science, engineering, or medical fields; understanding of research design, methodology, and statistics.
+ Thorough understanding of the EU MDR 2017/745, MDD 93/42/EEC; AIMDD 90/385/EEC; MEDDEV 2.7/1 Rev 4, MDCG Guidances on clinical evaluations, SSCP, PMCF plans and reports, and other international harmonized standards and guidelines related to medical devices, clinical studies, and quality systems.
+ Project management and/or management of people experience.
+ Strong presentation skills in relevant areas of clinical/technical applications.
+ Strong command of medical and surgical terminology.
+ Demonstrated ability to identify and adapt to shifting priorities and competing demands.
+ Highly developed interpersonal skills, and strong attention to detail.
+ 5-7+ years of experience in clinical research, clinical affairs, regulatory affairs, or quality systems, in the medical device or pharmaceuticals industry.
+ 3-5+ years of experience writing, reviewing or leading development of CERs and related documents in accordance with MEDDEV 2.7/1 Rev 3 and 4, the medical device directives (MDD 93/42/EEC; AIMDD 90/385/EEC) and the EU MDR 2017/745.
+ Certification is a plus (e.g., RAC and PMP).
**Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** ( your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at , on Facebook at and on Twitter @AbbottNews.
The base pay for this position is $75,300.00 - $150,700.00. In specific locations, the pay range may vary from the range posted.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Tiger Analytics is an advanced analytics consulting firm. We are the trusted analytics partner for several Fortune 100 companies, enabling them to generate business value from data. Our consultants bring deep expertise in Data Science, Machine Learning and AI. Our business value and leadership has been recognized by various market research firms, including Forrester and Gartner.

If you are passionate to work on unstructured business problems that can be solved using data, we would like to talk to you.

We are seeking a highly experienced and skilled Senior Lead Technology Consultant with over 12 years of overall technology consulting experience to join our team. The ideal candidate will possess exceptional communication and presentation skills, capable of effectively engaging with senior management stakeholders.

Requirements

• Lead and contribute to technology consulting engagements, providing expert advice and solutions.
• Develop and deliver compelling presentations to senior management, effectively communicating complex technical concepts and recommendations.
• Excellent analytical skills to identify potential issues and propose solutions by effectively conveying technical information to diverse teams.
• Collaborate with clients to understand and define their business needs, even when requirements are initially unstructured.
• Partner with analytics and technology consulting teams to share insights on key processes, personas, and tools, ensuring alignment on effective solutions.
• Ability to stay updated on industry trends and emerging technologies.
• Design and implement data solutions using technical tools.
• Mentor junior team members and contribute to the growth of our consulting practice.

Qualifications:

• Highly organised, self-motivated, and detail-oriented with the ability to operate in a fast-paced environment.
• 12+ years of proven experience in technology consulting.
• Exceptional written and verbal communication skills.
• Excellent problem solving and critical thinking skills with diligence.
• Demonstrated ability to develop high-quality presentations for senior management discussions.
• Proficiency in Databricks and SQL.
• Ability to thrive in environments with unstructured requirements and ambiguity.
• Experience with insurance or health payer data preferred.

Benefits

Significant career development opportunities exist as the company grows. The position offers a unique opportunity to be part of a small, fast-growing, challenging and entrepreneurial environment, with a high degree of individual responsibility.