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Meditech Project Jobs (NOW HIRING)

... MEDITECH functionality. Participate in process improvement initiatives and organizational transformation projects. Project Management & Implementation Lead and participate in projects through ...

CareSync Core Team Lead

Rome, NY · On-site

$50K - $105K/yr

These individuals will partner with MEDITECH, Rome Health leadership, project teams, application analysts, and operational stakeholders to ensure that departmental workflows, requirements, and ...

Pharmacist Go Live Support

$59.50 - $71.75/hr

Collaborate with project teams to provide onsite go-live support for MEDITECH Expanse implementation projects across HCA Healthcare facilities. * Participate in workflow decisions and trainings.

CareSync Core Team Lead

Rome, NY · On-site

$120 - $150/hr

These individuals will partner with MEDITECH, Rome Health leadership, project teams, application analysts, and operational stakeholders to ensure that departmental workflows, requirements, and ...

New

These individuals will partner with MEDITECH, Rome Health leadership, project teams, application analysts, and operational stakeholders to ensure that departmental workflows, requirements, and ...

$110 - $140/hr

These individuals will partner with MEDITECH, Rome Health leadership, project teams, application analysts, and operational stakeholders to ensure that departmental workflows, requirements, and ...

New

CareSync Core Team Lead

Rome, NY · On-site

$50K - $105K/yr

These individuals will partner with MEDITECH, Rome Health leadership, project teams, application analysts, and operational stakeholders to ensure that departmental workflows, requirements, and ...

Showing results 41-60

Meditech Project information

See salary details

$47K

$107.1K

$190K

How much do meditech project jobs pay per year?

As of Aug 20, 2026, the average yearly pay for meditech project in the United States is $107,124.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $125,500.00 per year, depending on experience, location, and employer.

What is a Meditech project?

A Meditech Project refers to the implementation, upgrade, or optimization of Meditech’s healthcare information technology systems within a healthcare organization. These projects often involve coordinating with clinical, administrative, and IT teams to deploy electronic health records (EHR), improve workflows, and ensure regulatory compliance. Meditech Projects require careful planning, data migration, staff training, and ongoing support to ensure a smooth transition and maximize system benefits. Project managers and analysts play key roles in leading these initiatives and ensuring project goals are met on time and within budget.

What are the key skills and qualifications needed to thrive as a Meditech project manager?

To excel as a Meditech Project Manager, you need strong project management skills, experience in healthcare IT, and familiarity with Meditech EHR systems, often supported by a relevant degree and PMP certification. Proficiency in Meditech modules, project management software, and healthcare compliance tools is typically required. Exceptional communication, problem-solving, and leadership skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial for ensuring successful Meditech implementations that meet organizational goals and regulatory standards.

What are some common challenges faced when managing a Meditech project, and how can they be addressed?

Managing a Meditech Project often involves navigating complex workflows, integrating with existing hospital systems, and ensuring user adoption among clinical staff. Challenges can arise from data migration, aligning project timelines with hospital operations, and managing stakeholder expectations. To address these, successful project managers prioritize clear communication, thorough training, and phased implementation strategies. Collaborating closely with IT teams, clinicians, and vendors helps ensure smoother transitions and minimizes disruption to patient care.

What is the difference between Meditech Project vs Meditech Analyst?

AspectMeditech ProjectMeditech Analyst
CertificationsProject Management certifications (PMP, CAPM)Meditech certifications, healthcare IT certifications
Work EnvironmentProject teams, healthcare IT implementation sitesHealthcare facilities, IT support teams
Employer & IndustryHospitals, healthcare providers, IT consulting firmsHospitals, healthcare organizations, software vendors

Meditech Project roles focus on managing healthcare IT implementations, coordinating teams, and ensuring project delivery. Meditech Analysts primarily analyze, configure, and support Meditech systems within healthcare settings. While both roles require healthcare IT knowledge, project managers oversee timelines and resources, whereas analysts handle system functionality and troubleshooting.

More about Meditech Project jobs

What are the most commonly searched types of Meditech Project jobs?

The most popular types of Meditech Project jobs are:

Infographic showing various Meditech Project job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $107,124 per year, or $51.5 per hour.

Senior R&D Engineer - MediTech (Mitsubishi Chemical Advanced Materials)

Mitsubishichemicalgroup

Fort Wayne, IN • Hybrid

Full-time

Posted 8 days ago


Job description

Company:

Mitsubishi Chemical Advanced Materials Inc.

Job Description:

Are you an experienced R&D engineer with a passion for medical innovation and implantable materials? Mitsubishi Chemical Advanced Materials is seeking a Senior R&D Engineer to join our MediTECH Division, where you'll help develop the next generation of orthopedic implant materials and manufacturing technologies.

This is a highly technical, customer-facing leadership role that combines research, product development, project management, and process engineering. You'll lead new product and process development from concept through commercialization while collaborating with customers, suppliers, and cross-functional teams to bring innovative medical device solutions to market. If you're driven by solving complex engineering challenges and advancing healthcare technologies, we'd love to hear from you.

What You'll DoLead New Product & Process Development
  • Lead research and development projects from concept through commercialization
  • Develop innovative implantable material solutions for orthopedic surgical applications
  • Design, execute, and document product and process development trials using laboratory and production equipment
  • Evaluate new technologies, manufacturing methods, and materials that support business growth
  • Prepare process, manufacturing, cost, and economic models to support new product initiatives
Drive Technical Innovation
  • Lead technical evaluations, implementation activities, and process validations for new products
  • Develop manufacturing methods, equipment specifications, and statements of work for production and development programs
  • Analyze complex materials and manufacturing challenges using engineering principles and data analytics
  • Support technology transfer, manufacturing scale-up, and process optimization activities
Lead Cross-Functional Projects
  • Serve as project manager for capital projects related to product development
  • Partner with Manufacturing, Quality, Design Engineering, and CAE teams to optimize product designs and manufacturing processes
  • Provide engineering support during production scale-up, troubleshooting, and process improvements
  • Assist laboratory personnel in developing new testing methods and validation protocols
Partner with Customers & Industry Leaders
  • Serve as the technical liaison for customers, suppliers, and external partners
  • Lead customer, supplier, and vendor interactions related to product development and validation
  • Represent MediTECH through ASTM, ORS, Biomaterials organizations, and other professional societies
  • Deliver technical presentations and publish papers that position Mitsubishi Chemical as an industry leader
Ensure Quality & Regulatory Excellence
  • Support product development activities in accordance with FDA Quality System Regulations and applicable ISO standards
  • Prepare technical reports, validation documentation, and engineering records
  • Maintain confidentiality while ensuring compliance with quality, regulatory, and customer requirements
  • Contribute to risk assessments, design controls, and technical documentation throughout the product lifecycle
What We're Looking For
  • Bachelor's degree in Engineering or a related technical discipline
  • 5+ years of experience in the orthopedic or medical device industry
  • Experience leading product development and engineering projects from concept through commercialization
  • Strong understanding of engineering principles related to product design, materials, and manufacturing processes
  • Experience reading and interpreting customer specifications and engineering drawings
  • Demonstrated project management experience with the ability to manage multiple priorities simultaneously
  • Strong analytical skills with experience using engineering and statistical analysis software, including Minitab
  • Excellent technical writing, presentation, and communication skills
  • Ability to collaborate effectively with customers, suppliers, and cross-functional teams
  • Self-motivated with strong leadership and organizational skills
  • Proficiency with Microsoft Office and collaboration tools such as Microsoft Teams
Preferred Qualifications
  • Experience with medical device design controls (21 CFR 820.30)
  • Knowledge of FDA Quality System Regulations and ISO 13485
  • Experience with ISO 10993 biocompatibility standards
  • Knowledge of ISO 14971 risk management processes
  • Experience with Design History Files (DHF) and medical device documentation
  • Experience with implantable device materials, including metals, polymers, and surface treatments
  • Experience creating FDA Master Files
  • Background in orthopedic implant materials or surgical applications
Work Arrangement & Travel
  • On-site or Hybrid opportunity
  • Hybrid schedule requires a minimum of three days per week on-site in Fort Wayne, IN
  • Less than 25% travel
Why Join Us?
  • Develop innovative materials that improve patient outcomes around the world
  • Lead high-impact R&D projects from concept through commercialization
  • Collaborate with experts in engineering, manufacturing, quality, and regulatory affairs
  • Represent Mitsubishi Chemical within leading medical and biomaterials organizations
  • Help shape the future of orthopedic implant technologies
  • Join a global organization committed to innovation, quality, and scientific excellence
  • Competitive compensation and comprehensive benefits package

If you're a technically driven engineer with a passion for medical device innovation, product development, and solving complex engineering challenges, we encourage you to apply and help shape the future of orthopedic materials and technologies.

The salary range for this position is $100,922 - $126,152 USD Annual. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills, internal peer equity, as well as market and business considerations may influence base pay offered. This salary will be subject to a geographic adjustment (according to a specific city and state), if an authorization is granted to work outside of the location listed in this posting.

All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status

Mitsubishi Chemical Advanced Materials Inc. is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please email MCA-MBX_accomodations@m-chem.com.We will make a determination on your request for reasonable accommodation on a case-by-case basis.

The law requires Mitsubishi Chemical Advanced Materials Inc. to post a notice describing the Federal laws prohibiting job discrimination. For information regarding your legal rights and protections, please click on the following link: Know Your Rights

Mitsubishi Chemical Advanced Materials Inc. will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay. Please see the Pay Transparency Nondiscrimination Provision for more information

As a Federal Contractor, Mitsubishi Chemical Advanced Materials Inc. is required to participate in the E-Verify Program to confirm eligibility to work in the United States. For information please click on the following link: E-Verify.