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Associate Medical Device Labeling Jobs in Ohio (NOW HIRING)

Assembler_Cleanroom_Valve - Level 2

Solon, OH · On-site

$16.75 - $20.50/hr

The associate can perform some basic process changeovers and troubleshooting with some guidance or ... medical conditions, age, national origin or ancestry, disability, genetic information, veteran ...

Associate's degree and 8 years of experience in Quality and/or Manufacturing in the pharmaceutical, biotech or medical device industries OR * High school diploma / GED and 10 years of experience in ...

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Associate Medical Device Labeling information

What are some common challenges faced by associate medical device labeling, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

What is an associate medical device labeling?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.

What are the key skills and qualifications needed to thrive as an associate medical device labeling?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.
What are the most commonly searched types of Medical Device Labeling jobs in Ohio? The most popular types of Medical Device Labeling jobs in Ohio are:

Senior Principal Mechanical Design Engineer

Stress Engineering Services Inc.

Mason, OH • On-site

$150 - $190/hr

Other

Medical, Dental, Vision, PTO

Posted 5 days ago


Job description

Career Opportunities with Stress Engineering Services Inc.

A great place to work.

Careers At Stress Engineering Services Inc.

Are you ready for new challenges and new opportunities?

Current job opportunities are posted here as they become available.

Senior Principal Mechanical Design Engineer

Senior Principal Mechanical Design Engineer

Are you the engineer others call when the design challenge seems impossible?

Can you lead multidisciplinary teams and guide clients through the complexities of medical device development and commercialization?

Do you want to apply your expertise across surgical devices, drug delivery systems, diagnostics, and emerging healthcare technologies?

About Stress Engineering Services

Stress Engineering Services (SES) is an elite, one‑of‑a‑kind engineering consulting firm, trusted for more than 50 years to solve the problems others can’t. Our reputation is built on an uncompromising commitment to technical excellence, a highly selective team of experts, and a track record of delivering answers in the most complex, high‑stakes environments. We operate at the intersection of deep technical expertise and real‑world application, partnering with clients across energy, aerospace, consumer products, medical, and beyond. Our teams combine advanced analysis with hands‑on testing, failure analysis, and practical engineering judgment to deliver solutions that perform where it matters most—in the field. As an employee‑owned company, our people are personally invested in every outcome, creating a culture where accountability is high and excellence is the standard. We don’t just solve problems we uncover root causes, mitigate risk, and deliver confidence.

For our clients, that means a trusted partner known for rigor and results. For our people, it means joining an elite team tackling the most meaningful challenges in engineering.

SES is where complex problems meet uncommon solutions—and where elite engineers come to do their best work.

Our Core Values

  • We Over Me – We put the mission, our clients, and our team ahead of individual agendas
  • Unyielding Pursuit of Excellence – Excellence is the standard. We deliver the right solution, on time, every time
  • Own It – We take accountability to earn trust and deliver results

The Opportunity

We are seeking a Senior Principal Mechanical Design Engineer to join our Industrial & Product Design team with a primary focus on medical device and healthcare product development.

This is a senior‑level consulting and technical leadership role for a recognized engineering expert who thrives on solving complex product development challenges in highly regulated environments. As one of the firm's most experienced engineers, you will lead multidisciplinary teams, mentor talented technical associates and engineers, and serve as a trusted advisor to clients developing next‑generation medical devices, surgical technologies, drug delivery systems, diagnostic products, and other healthcare solutions.

You will guide projects from early innovation and concept development through design verification, validation, regulatory submission support, manufacturing transfer, and commercialization.

Success in this role requires deep expertise in mechanical design, product development, risk management, human factors, and engineering within regulated medical device environments.

Technical Leadership

  • Serve as a senior technical authority for medical device and healthcare product development programs.
  • Lead and mentor a team of talented engineers, designers, and technical associates, fostering a culture of innovation, technical excellence, accountability, and continuous learning.
  • Provide technical oversight on the most complex client engagements involving medical devices, drug delivery systems, surgical instruments, diagnostics, and combination products.
  • Guide engineering teams through challenging design decisions, risk assessments, and regulatory requirements.
  • Conduct high‑level design reviews and provide technical leadership throughout the product development lifecycle.
  • Support recruiting, mentoring, coaching, and development of future technical leaders within SES.

Medical Device Product Development & Design Excellence

  • Lead the design and development of Class I, II, and III medical devices from concept through commercialization.
  • Design Controls
  • Verification & Validation
  • Design for Manufacturability (DFM)
  • Design for Assembly (DFA)
  • Reliability Engineering
  • Product Lifecycle Management
  • Develop innovative solutions for surgical, orthopedic, cardiovascular, diagnostic, pharmaceutical, and drug delivery applications.
  • Lead cross‑functional teams through product development activities, including design reviews, failure investigations, testing strategies, and regulatory submissions.
  • Design and oversee development of prototypes, test fixtures, and verification methods.
  • Evaluate product performance using engineering analysis, testing, and data‑driven methodologies.
  • Serve as a trusted engineering advisor to medical device manufacturers, pharmaceutical companies, and healthcare technology organizations.
  • Lead executive‑level technical discussions with clients regarding product development strategies, design risks, testing approaches, and commercialization plans.
  • Present technical recommendations and engineering findings to technical, operational, quality, and executive stakeholders.
  • Support business development efforts and build long‑term relationships within the medical device and healthcare industries.

Basic Qualifications

  • Bachelor's, Master's, or PhD in Mechanical Engineering, Biomedical Engineering, or related engineering discipline from an ABET-accredited institution.
  • Professional Engineer (PE) license required.
  • 15+ years of progressive experience developing medical devices within regulated environments.
  • Extensive experience leading product development programs from concept through commercialization.
  • Demonstrated expertise in FDA-regulated product development processes and Design Controls.
  • Experience leading multidisciplinary engineering teams and mentoring technical professionals.
  • Strong understanding of product risk management, verification, validation, and quality systems.
  • Proven track record of successful client engagement and technical leadership.
  • Exceptional written, verbal, and presentation skills.
  • Ability and willingness to serve in a highly client‑facing consulting role.
  • Authorized to work in the United States without sponsorship.

Preferred Qualifications

  • Advanced degree (MS or PhD) in Mechanical Engineering, Biomedical Engineering, or related discipline.
  • Expertise with FDA, ISO 13485, IEC 60601, ISO 14971, and other applicable medical device standards.
  • Combination products
  • Pharmaceutical manufacturing equipment
  • Strong knowledge of human anatomy, physiology, and surgical procedures.
  • Experience supporting regulatory submissions and product approvals.
  • Advanced CAD proficiency (SolidWorks preferred).
  • Experience with statistical analysis, DOE, Python, MATLAB, Minitab, JMP, or similar tools.

What Makes You Successful in This Role

  • Recognized technical expert within the medical device industry.
  • Passionate mentor who enjoys developing engineers and technical associates.
  • Strong balance of innovation, engineering rigor, and practical execution.
  • Comfortable leading highly regulated, multidisciplinary product development efforts.
  • Trusted by clients for technical excellence, sound judgment, and strategic insight.
  • Driven to solve difficult healthcare challenges that improve patient outcomes and quality of life.

Why Join SES

  • Solve problems that matter – Your work directly impacts product performance, safety, and reliability
  • High autonomy + high ownership – You’re trusted to lead and deliver
  • Broad technical exposure – Work across industries, materials, and challenges
  • Collaborate with experts – Learn from recognized leaders in engineering and failure analysis
  • Entrepreneurial environment – Be part of a team that values initiative, curiosity, and innovation
  • Employee‑owned culture (ESOP) – Share in the success you help create
  • Thought Leadership - You’ll have the opportunity to contribute to meaningful engineering insights, share your expertise with the broader industry, and build credibility as a trusted technical voice.

What’s in it for you?
At Stress Engineering, curiosity isn’t just encouraged, it’s expected. You’ll have the opportunity to deepen your technical expertise, broaden your industry exposure, and make a meaningful impact on real‑world engineering challenges from day one.

We offer a comprehensive and competitive benefits package, including medical, dental, and vision coverage, paid time off, and holidays. Your compensation is thoughtfully aligned with your experience, expertise, and the value you bring to the team.

Own your impact. Build your future.
Here, employee ownership is more than a benefit—it’s part of our culture. The work you do today contributes to long‑term success that you share in, alongside a team that values collaboration, innovation, and accountability. We’re built for stability and growth, where your technical skills and problem‑solving directly influence outcomes—not just for individual projects, but for the future of the company. If you’re driven by meaningful work, a strong team, and the opportunity to think like an owner, you’ll thrive at Stress Engineering.

Recruitment Process Disclosure
As part of your candidacy and potential future employment, you agree to maintain the confidentiality of proprietary, sensitive, and client‑related information obtained through interactions with SES. This obligation applies during and after your engagement.

As part of our hiring process, Stress Engineering Services may use technology tools, including automated tools, to help organize, review, or evaluate application materials and interview‑related information. These tools are used to support our recruiting process, but hiring decisions are not made solely by technology. If you need would like to request a reasonable accommodation or would like additional information about the process, please contact Human.Resources@Stress.com . Where applicable required by law, we will provide additional notices if a specific tool analyzes interview responses, assessments, or other information as part of your evaluation.

Equal Opportunity Employer
Stress Engineering Services, Inc. (SES) is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other protected characteristics.

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