ZipRecruiter

Log In

1

Meditech Report Writer Jobs (NOW HIRING)

Humetis Group

Office Support Specialist I

Canton, MA · On-site

$19 - $25/hr

... Meditech face sheets when Case Managers make changes. * Prepares and distributes written and ... Reports maintenance issues electronically via the maintenance request form (CAMIS). * Assists ...

Forward Advantage

Solutions Engineer I

Fresno, CA · On-site

$60K - $80K/yr

Job Summary As a Solutions Engineer I on our IM-One team, you will report directly to the IM-One ... MEDITECH * Fundamental Knowledge of ALL MEDITECH Versions and their Fundamental Clinical Workflow ...

Orthoindy

Hospital Access Coordinator II

Carmel, IN · On-site

$16.75 - $21.25/hr

... orthotalent, incident reporting, meditech, microsoft office, theraoffice, insurance systems ... and written communication skills and high level of accuracy and attention to detail a must ...

Orthoindy

Hospital Access Coordinator II

Greenwood, IN · On-site

$15.50 - $19.50/hr

ADP, Allscripts, OrthoTalent, Incident reporting, Meditech, Microsoft Office, Athena, TheraOffice ... Exceptional verbal and written communication skills and high level of accuracy and attention to ...

Merrimack Health

Payroll Administrator

Lawrence, MA · On-site

$25.75 - $34.50/hr

Responsibility for processing, review and data entry in both ADP and Meditech systems. Processing ... AD Hoc reporting as needed (Examples FTE reporting, audit requests, various salary reports)

Merrimack Health

Payroll Administrator

Lawrence, MA · On-site

$25.75 - $34.50/hr

Responsibility for processing, review and data entry in both ADP and Meditech systems. Processing ... AD Hoc reporting as needed (Examples FTE reporting, audit requests, various salary reports)

previous pagenext page

Showing results 21-40

All JobsMeditech Report Writer Jobs

Meditech Report Writer information

See salary details

$18K

$76.6K

$185.5K

How much do meditech report writer jobs pay per year?

As of Sep 8, 2026, the average yearly pay for meditech report writer in the United States is $76,608.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $94,500.00 per year, depending on experience, location, and employer.

What is a Meditech report writer?

A Meditech Report Writer is responsible for designing, developing, and maintaining reports within the Meditech electronic health record (EHR) system. They work with healthcare data, pulling information from Meditech databases to create reports used for clinical, financial, and operational decision-making. This role requires knowledge of Meditech reporting tools, SQL, and database structures to ensure reports are accurate and efficient. Meditech Report Writers collaborate with healthcare professionals to understand reporting needs and provide solutions that improve data-driven decision-making.

What does a Meditech report writer do?

A typical day for a Meditech Report Writer involves gathering reporting requirements from clinical and administrative staff, developing and maintaining customized reports using Meditech’s reporting tools, and troubleshooting any data discrepancies or technical issues that arise. You’ll often collaborate with IT teams, analysts, and end-users to ensure reports meet organizational needs and adhere to compliance standards. Regular responsibilities may also include providing training or support to users on how to access and interpret reports, as well as documenting processes for future reference. The work environment is usually fast-paced and detail-oriented, with opportunities to make a direct impact on process improvement and data-driven decision-making within the healthcare organization.

What are the key skills and qualifications needed to thrive as a Meditech report writer?

To thrive as a Meditech Report Writer, you need a solid understanding of healthcare data, report development, and knowledge of healthcare workflows, usually supported by a background in health information management or IT. Proficiency in Meditech reporting tools, SQL query writing, and familiarity with EHR systems are typically required, and some employers may prefer certification in Meditech applications or related healthcare IT technologies. Strong analytical skills, attention to detail, effective communication, and the ability to collaborate across departments are key soft skills in this role. These skills ensure accurate data analysis, efficient report delivery, and the ability to translate complex requirements into actionable reporting solutions for healthcare organizations.

More about Meditech Report Writer jobs

What cities are hiring for Meditech Report Writer jobs?

Cities with the most Meditech Report Writer job openings:

What states have the most Meditech Report Writer jobs?

States with the most job openings for Meditech Report Writer jobs include:

What job categories do people searching Meditech Report Writer jobs look for?

The top searched job categories for Meditech Report Writer jobs are:

Meditech Report Writer jobs near you
Infographic showing various Meditech Report Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $76,608 per year, or $36.8 per hour.

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

Mitsubishichemicalgroup

Fort Wayne, IN • Hybrid

Full-time

Posted 27 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.

Apply