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Quality Director In Medical Devices Jobs (NOW HIRING)

$84K - $100K/yr

Look around your home, and you'll find us everywhere, in your kitchen, living room, bedroom, and ... Perform component and system failure analysis with Quality. * Lead technical reviews and ...

New

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Familiarity with regulatory reporting requirements for medical devices (e.g. MDRs, Vigilance ... Bachelor's Degree in Electrical Engineering or Mechanical Engineering HIGHLY PREFERRED. Other ...

New

... director and clinical intensivist to join our critical care team at Conway Medical Center in Conway ... Employed model with health benefits- Hourly rate plus quality/RVU bonus and FMD stipend ...

NY · On-site

$84K - $100K/yr

Look around your home, and you'll find us everywhere, in your kitchen, living room, bedroom, and ... Perform component and system failure analysis with Quality. * Lead technical reviews and ...

New

Quality Engineer

Norristown, PA · On-site

$68K - $88K/yr

Direct and collaborate with supplier representatives on quality problems, ensure corrective action ... At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related ...

Quality Engineer

Norristown, PA · On-site

$68K - $88K/yr

Direct and collaborate with supplier representatives on quality problems, ensure corrective action ... At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related ...

TeamHealth is seeking a quality-driven physician to join our post-acute care team in Seattle ... Our Medical Director Leadership Academy (MDLA) will position you for success in quality improvement ...

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We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

Be Seen First

We are seeking a Quality Manufacturing Engineer extensive experience in Medical Devices to oversee Manufacturing Quality projects and line transfers for a Medical Device company. The perfect ...

Showing results 41-60

Quality Director In Medical Devices information

See salary details

$31K

$125.6K

$213.5K

How much do quality director in medical devices jobs pay per year?

As of Sep 13, 2026, the average yearly pay for quality director in medical devices in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Quality Director In Medical Devices jobs?

For Quality Director In Medical Devices jobs, the most frequently searched job titles are:

Operations Product Engineer, Medical Devices

On-site

Helen of Troy
Manufacturing • 1 - 5K employees

$84K - $100K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Helen Of Troy rating

8.3

Company rating: 8.3 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Join our Engineering team at Helen of Troy and make an immediate impact on our trusted brands: Braun, Vicks. Together, we build innovative and useful products that elevate people's lives everywhere every day.

Look around your home, and you'll find us everywhere, in your kitchen, living room, bedroom, and bathroom. We are already making your everyday lives better. We are powered by knowledgeable, enthusiastic, and forward-thinking people committed to developing a culture of inclusion. Whether you are just starting your career or in need of a challenge, we recognize, develop, and empower talent!

Position:

Operations Product Engineer, Medical Devices

Department:

Engineering (Braun, Vicks)

Work Location(s):
  • Marlborough, MA
  • New York, NY
Hybrid Schedule:

At Helen of Troy, we embrace a flexible hybrid work model designed to support collaboration and productivity. For roles eligible for hybrid work, our standard schedule includes in-office collaboration from Tuesday through Thursday, with the option to work remotely on Mondays and Fridays. Any updates to this model will be communicated in advance. Please note that hybrid eligibility and schedules may vary based on business needs and manager expectations.

What you will be doing:

The Operations Product Engineer will serve as the primary technical owner for sustaining engineering activities on assigned consumer medical products (Braun and Vicks products).This role will be responsible for developing test plans, reviewing test reports and process validation documents, and drafting technical memos for medical products to ensure they meet intended use and specification needs.

A major component of this role will be supporting sustaining engineering projects through technical investigations, design changes, documentation updates, and cross-functional problem solving.

  • Maintain DHF documentation and design history records for existing products.
  • Assess product changes and determine required verification, validation, and documentation activities
  • Work with engineering, program management, regulatory, quality, supply chain and marketing teams on sustaining engineering
  • Perform component and system failure analysis with Quality.
  • Lead technical reviews and verification testing.
  • Work with accredited test laboratories to support product testing and regulatory compliance activities, including biocompatibility, electrical safety, and performance evaluations.
Skills needed to be successful in this role:
  • Strong communication skills with the ability to deliver clear, concise project updates and direction to technical and non-technical audiences, including non-native English speakers.
  • Ability to manage multiple priorities in a fast-paced environment while remaining flexible and adaptable.
  • Proactive, self-driven mindset with a strong sense of ownership and initiative.
  • Strong problem-solving skills, attention to detail, and commitment to quality.
  • Self-motivated learner with a track record of independently developing new technical skills and knowledge to solve engineering challenges.
  • Collaborative team player who thrives in cross-functional environments.
  • Passion for applying engineering expertise to drive meaningful business impact.
Minimum Qualifications:
  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related technical field.
  • 2+ years of experience in sustaining engineering, product development, and/or manufacturing.
  • Experience working within a regulated industry.
  • Experience supporting healthcare consumer products, consumer electronics products, medical devices or similar electromechanical products.
  • Knowledge of ISO 13485 and IEC 60601 standards.
  • Proficiency with CAD tools (SolidWorks, Creo, or similar), prototyping, and 3D printing.
  • Experience with manufacturing processes, including injection molding, sheet metal fabrication, silicone molding, and die casting.
  • Ability to travel domestically/internationally up to 15% (China, Mexico, Thailand, and Vietnam).
  • Authorized to work in the United States on a full-time basis.
Preferred Qualifications:
  • Familiarity with software and firmware development concepts and ability to collaborate with software engineering teams
  • Understanding of UL/ETL/FDA/CE/NMPA general requirements.
  • Hands on Circuit Design and PCBA experience.

In Massachusetts and New York, the standard base pay range for this role is $84,000 -$100,000 annually. This base pay range is specific to Massachusetts/New York and may notbe applicableto other locations. Actual salaries will vary based on several factors, including but not limited to location, experience, skill level, and performance. The range listed is just onecomponentof the total compensation package for employees.

Benefits:
  • Salary + Bonus
  • Healthcare
  • Dental
  • Vision
  • Paid Holidays
  • Paid Parental Leave
  • 401(k) with company match
  • Basic Life Insurance
  • Short Term Disability (STD)
  • Long Term Disability (LTD)
  • Paid Time Off (PTO)
  • Paid Charitable (volunteer)
  • Leave, and Educational Assistance.

For more information about Helen of Troy, visit www.helenoftroy.com. You can also find us on LinkedIn, and Glassdoor.

Helen of Troy is an EqualOpportunity/AffirmativeAction Employer. We are committed tofostering a diverse and inclusive workplace where all employees can thrive. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category under applicable federal, state, and local laws.

We will provide individuals with disabilities with reasonable accommodations to participate in the job application process. To request an accommodation, please contact Human Resources at (915) 225-8000.

Founded in 1968, Helen of Troy is a leading global consumer products company with operations acrossNorthAmerica, South America, Europe, and Asia.Our portfolio includes trusted brandssuch as OXO, Hydro Flask, Osprey, Honeywell, PUR, Braun, Vicks, Hot Tools, Drybar, Curlsmith, Revlon, and Olive & June – many of which rankamong the top brands in their consumer goods categories.

We grow and strengthen our brands through innovation, operational excellence, and a collaborative culture focused on delivering exceptional products and experiences for consumers worldwide.

The above statements are intended to describe the general nature and level of work performedand are not intended to be an exhaustive list of responsibilities.

Managementreservesthe right tomodify the duties and responsibilitiesof the position at any time.

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