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Autonomous Medical Devices Incorporated Jobs in Ohio

ALTEN Technology USA

$80K - $90K/yr

We're ALTEN Technology USA, an engineering company helping clients bring groundbreaking ideas to life-from advancing space exploration and life-saving medical devices to building autonomous electric ...

ALTEN Technology USA

Mechanical Engineer II

Twinsburg, OH · On-site

$80K - $100K/yr

We're ALTEN Technology USA, an engineering company helping clients bring groundbreaking ideas to life-from advancing space exploration and life-saving medical devices to building autonomous electric ...

ALTEN Technology USA

Mechanical Engineer II

Twinsburg, OH · On-site

$85K - $100K/yr

We're ALTEN Technology USA, an engineering company helping clients bring groundbreaking ideas to life-from advancing space exploration and life-saving medical devices to building autonomous electric ...

ALTEN Technology USA

Mechanical Engineer II

Twinsburg, OH · On-site

$85K - $100K/yr

We're ALTEN Technology USA, an engineering company helping clients bring groundbreaking ideas to life--from advancing space exploration and life-saving medical devices to building autonomous electric ...

TL Worldwide Transportation

NEMT Driver

Akron, OH · On-site

$18 - $22/hr

... Transit Incorporated is looking for dependable, compassionate drivers who want more than just a ... As a Non-Emergency Medical Transportation Driver, you will help passengers safely travel to medical ...

SCA Health

Medical Assistant

West Chester, OH · On-site

$16.75 - $21.50/hr

... autonomy. What sets SCA Health apart isn't just what we do, it's how we do it . Each decision we ... Apply and remove orthopedic devices such as splints, braces, and casts under provider supervision.

SCA Health

Medical Assistant

Cincinnati, OH · On-site

$28/hr

... autonomy. What sets SCA Health apart isn't just what we do, it's how we do it . Each decision we ... Apply and remove orthopedic devices such as splints, braces, and casts under provider supervision.

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Autonomous Medical Devices Incorporated information

What is the difference between Autonomous Medical Devices Incorporated vs Medical Device Technician?

AspectAutonomous Medical Devices IncorporatedMedical Device Technician
CredentialsRelevant certifications, such as biomedical equipment technician (CBET)Certifications like CBET or equivalent often required
Work EnvironmentDesign, development, and testing of autonomous medical devices in labs or officesMaintenance, repair, and installation in hospitals or clinics
Industry UsageResearch and innovation in autonomous medical technologyOperational support and troubleshooting of medical devices

While Autonomous Medical Devices Incorporated focuses on developing autonomous medical technology, Medical Device Technicians primarily handle the maintenance and repair of existing devices. Both roles require technical certifications and work within the healthcare industry, but their daily tasks and environments differ significantly.

What are some common challenges faced by professionals working at Autonomous Medical Devices Incorporated, and how can they be addressed?

Professionals at Autonomous Medical Devices Incorporated often face challenges related to the fast-paced nature of medical technology innovation, such as keeping up with regulatory requirements, ensuring product quality, and collaborating across interdisciplinary teams. Adapting to constant advancements in the field and communicating effectively with engineers, clinicians, and regulatory experts are essential. To address these challenges, team members benefit from ongoing professional development, regular cross-functional meetings, and leveraging project management tools to keep projects on track and compliant.

What are the key skills and qualifications needed to thrive as an Autonomous Medical Devices engineer, and why are they important?

To thrive as an Autonomous Medical Devices Engineer, you need a strong background in biomedical engineering, robotics, and systems integration, typically supported by a relevant engineering degree. Familiarity with medical device regulations, CAD software, embedded systems, and programming languages such as Python or C++ is essential. Strong problem-solving skills, attention to detail, and effective communication are vital for collaborating with cross-functional teams and ensuring patient safety. These competencies are crucial for designing reliable, innovative devices that meet regulatory standards and improve healthcare outcomes.

What is Autonomous Medical Devices Incorporated?

Autonomous Medical Devices Incorporated (AMDI) is a company specializing in the development and manufacturing of automated medical devices and diagnostic solutions. Their focus is on creating innovative, user-friendly products that enhance healthcare delivery by automating processes such as testing and diagnostics. AMDI's technologies are designed to improve efficiency, accuracy, and accessibility in medical settings, often incorporating robotics and artificial intelligence. The company works with healthcare providers, laboratories, and research institutions to bring advanced automation to clinical workflows.

What are popular job titles related to Autonomous Medical Devices Incorporated jobs in Ohio?

For Autonomous Medical Devices Incorporated jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Autonomous Medical Devices Incorporated jobs in Ohio look for?

The top searched job categories for Autonomous Medical Devices Incorporated jobs in Ohio are:

What cities in Ohio are hiring for Autonomous Medical Devices Incorporated jobs?

Cities in Ohio with the most Autonomous Medical Devices Incorporated job openings:

Autonomous Medical Devices Incorporated jobs near you
Infographic showing various Autonomous Medical Devices Incorporated job openings in Ohio as of August 2026, with employment types broken down into 70% Full Time, 14% Part Time, and 16% Contract. Highlights an 86% In-person, and 14% Remote job distribution.

Sr. Engineer, Combination Products & Medical Device

Hikma Pharmaceuticals PLC

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago

Hikma Pharmaceuticals rating

8.0

Company rating: 8.0 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical

Job description

Job Title: Sr. Engineer, Combination Products & Medical Device
Location: Columbus, OH
Job Type: Full time
Req ID: 11621
About Us:
As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Sr. Engineer, Combination Products & Medical Device to join our team.
In this role, you will be responsible for providing Combination Product and Medical Device Quality System Framework and Design expertise both within local operations and to drive best practices within the global organization.
Support includes ensuring that all applicable Combination Product and Medical Device regulations are incorporated within corporate and local procedures and are adequately implemented within the manufacturing site.
Responsibility also includes assessing, evaluating, identifying and implementing required documentation and studies to support requirements for launch, lifecycle changes and Business Development opportunities to meet identified business objectives and targets.
Key Responsibilities:
Knowledge Management
  • Stay up to date on regulations and regulatory trends to ensure that practices and procedures remain current with regulatory health authorities' expectations with regards to Combination Products and Medical Devices i.e. 21 CFR Part 820 QSR, 21 CFR Part 4, ISO 13485, ISO14971, etc...
  • Supports Combination Product and Medical Device inspection readiness and regulatory inspection responses as needed
  • Active member of relevant industry groups and key stakeholder organizations
  • Direct the work of consultants as needed and mentor others
  • Responsible for driving site education with regards to combination products and medical device requirements and organizational processes.

Infrastructure Support
  • Develop and ensure lifecycle management of a Quality Management System to be compliant with all relevant combination product and medical device regulations
  • Work within a Center of Excellence to share and align on best practices across Hikma Operating Units
  • Facilitate and/or supports the development and implementation of combination product and medical device quality governance processes and procedures
  • Develops and drives Risk Management approach
  • Contributes in relevant Quality Governance meetings

Project Support
  • Leads and/or participates on departmental and/or cross-functional teams as Combination Product and Medical Device SME
  • Performs gap assessments of processes and procedures against relevant device regulations
  • Develops recommendations and proposals to address identified gaps and provides expert guidance for projects
  • Drives, as appropriate, key activities such as risk analysis, FMEA and threshold analysis for active projects
  • Drive required Statements of Work with consultants where needed to support specific product programs e.g. device reliability, human factor studies, threshold analysis, FMEA, and/or risk analysis
  • Drives change control support for Combination Product & Medical Device requirements assessment and deliverable review
  • Provide support for relevant investigations and CAPA(s)
  • Provides guidance on approach and regulatory responses support for health authority questions to support product approvals
  • Other duties as assigned
  • Predictable, consistent onsite attendance required

Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
  • B.S. in engineering field (e.g. pharmacy, chemical, medical device, packaging or mechanical) with 10+ years direct experience at a medical device manufacturer or combination product manufacturer
  • M.S. in engineering field with 5+ years direct experience at a medical device manufacturer or combination product manufacturer

Business & Technical Expertise
  • Strong understanding of business development, lifecycle management, and long-term planning.
  • Subject matter expert in combination products and medical devices, including design controls, risk management, validation, reliability, and process controls.
  • Deep knowledge of pharmaceutical principles and complex dosage forms (e.g., nasal suspensions, dry powder inhalers, novel delivery systems).
  • Experienced in manufacturing, packaging, and device production processes.

Customer Focus
  • Champions quality and customer service excellence.
  • Aligns strategies to customer needs and market trends.
  • Establishes best practices to maintain industry-leading service standards.

Innovation & Change Leadership
  • Promotes a culture of innovation and continuous improvement.
  • Evaluates solutions against business goals and stakeholder impact.
  • Drives actionable strategies that enhance productivity and competitive advantage.

Communication & Influence
  • Effective communicator across diverse audiences; skilled in presentations, technical writing, and meeting facilitation.
  • Proficient in Microsoft Office tools (Word, Excel, PowerPoint, Outlook).

Regulatory & Operational Excellence
  • Expert knowledge of pharmaceutical regulations (cGMP, FDA, DEA, ANDA requirements).
  • Strong project management experience leading cross-functional teams.
  • Able to work independently with minimal supervision.

Preferred Qualifications:
  • Experience with Class III/lifesaving combination products or medical devices; background in statistics and continuous improvement (Six Sigma Green/Black Belt preferred).
  • Strong critical thinking skills with a track record of completing complex projects and developing solutions to minimize risk and resolve issues.
  • Proven ability to manage multiple high-complexity projects, influencing cross-functional teams (PD, AD, DRA, Medical, QA, Operations, Warehouse) and external partners while meeting strict timelines.
  • Demonstrated decision-making capability, balancing risk vs. reward and independently driving tactical decisions (e.g., formulation, manufacturing processes, QbD strategy, experimental design).
  • Contributes to project planning, timelines, and budget adherence aligned with business goals.
  • Decisions primarily impact local operations with potential regional/global implications, including influence on regulatory timelines and product launch readiness.
  • Evaluates scientific and business risks to guide innovation and strategic direction.

What We Offer*:
  • Annual performance bonus, commission, and share potential
  • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
  • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
  • 3 personal days (prorated based on hire date)
  • 11 company paid holidays
  • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
  • Employee discount program
  • Wellbeing rewards program
  • Safety and Quality is a top organizational priority
  • Career advancement and growth opportunities
  • Tuition reimbursement
  • Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
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