1

Costa Rica Medical Device Quality Jobs (NOW HIRING)

Senior Quality Specialist

Arden Hills, MN · Hybrid

$86K - $119K/yr

Costa Rica-Coyol; Costa Rica-Heredia; US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove ... Strong understanding of medical device Quality System directives, regulations, and standards.

Senior Quality Specialist

Arden Hills, MN · Hybrid

$83K - $114K/yr

Costa Rica-Coyol; Costa Rica-Heredia; US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove ... Strong understanding of medical device Quality System directives, regulations, and standards.

Medical Device Quality Inspector Location: Madison, WI (Onsite) Pay Rate: $25-30/hr. on W2 **Opportunity to earn overtime pay** The Medical Device Quality Inspection group is responsible for assuring ...

Medical Device Quality Engineer Location: Madison, WI Pay Rate : $40--45/hr on W2 Schedule: Onsite, Monday-Friday (standard business hours) Summary The Senior Quality Analyst/Engineer is responsible ...

Quality Engineer

Attleboro Falls, MA · On-site

$97K - $115K/yr

... Costa Rica, Texas, and Massachusetts. Theragenics proudly operates Arrotek, a visionary medical ... Minimum 3 years experience in medical device industry in the capacity of quality engineering ...

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

Quality Engineer

Attleboro Falls, MA · On-site

$97K - $115K/yr

... Costa Rica, Texas, and Massachusetts. Theragenics proudly operates Arrotek, a visionary medical ... Minimum 3 years experience in medical device industry in the capacity of quality engineering ...

About the company: Viant is a global medical device partner providing design, development ... Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana ...

next page

Showing results 1-20

Costa Rica Medical Device Quality information

See salary details

$21

$36

$70

How much do costa rica medical device quality jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for costa rica medical device quality in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Quality roles in Costa Rica, and why are they important?

To thrive in a Medical Device Quality role in Costa Rica, you need a solid understanding of quality management systems, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and experience in medical device manufacturing. Familiarity with quality assurance tools, document control systems, and certifications like Six Sigma or ASQ Certified Quality Engineer are typically required. Strong attention to detail, analytical thinking, and effective teamwork and communication skills help individuals excel in this field. These competencies ensure products meet rigorous safety and regulatory standards, supporting both patient safety and company reputation.

What are some common challenges faced by professionals working in medical device quality roles in Costa Rica, and how can they be addressed?

Professionals in medical device quality roles in Costa Rica often face challenges related to navigating both local and international regulatory requirements, ensuring consistent product quality, and adapting to frequent updates in compliance standards. Effective communication and collaboration with cross-functional teams—such as engineering, production, and regulatory affairs—are crucial for addressing these challenges. Staying updated with global quality standards, participating in regular training, and utilizing robust quality management systems can help professionals maintain compliance and drive continuous improvement.

What is the difference between Costa Rica Medical Device Quality vs Costa Rica Medical Device Regulatory Affairs Specialist?

AspectCosta Rica Medical Device QualityCosta Rica Medical Device Regulatory Affairs Specialist
CertificationsISO 13485, internal quality auditsRegulatory compliance, local and international approvals
Work EnvironmentManufacturing sites, quality control labsRegulatory agencies, documentation review
Industry UsageQuality assurance, process improvementRegulatory submissions, compliance management

While both roles focus on ensuring medical device safety and compliance, Costa Rica Medical Device Quality primarily emphasizes quality assurance and process control within manufacturing. In contrast, Costa Rica Medical Device Regulatory Affairs Specialists handle regulatory submissions and ensure compliance with local and international regulations. Both roles are essential in the medical device industry but differ in their core responsibilities and daily tasks.

What are Costa Rica Medical Device Quality jobs?

Costa Rica Medical Device Quality jobs involve ensuring that medical devices manufactured or distributed in Costa Rica meet local and international quality standards and regulatory requirements. Professionals in these roles oversee quality assurance processes, conduct audits, manage compliance documentation, and collaborate with engineering and production teams to maintain product safety and effectiveness. These positions are crucial in the country's growing medical device sector, which is known for its adherence to strict quality and regulatory standards.
More about Costa Rica Medical Device Quality jobs
What cities are hiring for Costa Rica Medical Device Quality jobs? Cities with the most Costa Rica Medical Device Quality job openings:
What states have the most Costa Rica Medical Device Quality jobs? States with the most job openings for Costa Rica Medical Device Quality jobs include:
Infographic showing various Costa Rica Medical Device Quality job openings in the United States as of June 2026, with employment types broken down into 4% Full Time, 67% Part Time, 27% Temporary, and 2% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $76,384 per year, or $36.7 per hour.
Senior Quality Specialist

Senior Quality Specialist

Boston Scientific

Arden Hills, MN • Hybrid

$86K - $119K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 119 frontline employees who took The Breakroom Quiz

35th of 527 rated manufacturers


Job description

Additional Location(s):  N/A; Canada-ON-Mississauga; Costa Rica-Coyol; Costa Rica-Heredia; US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.       

About the role:

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.

The Senior Quality Specialist will be a member of the high-performing EP/CRM Quality Acquisition Integration Team, leading and supporting quality integration initiatives. This individual will serve as a key contributor in determining integration strategies related to the Boston Scientific Quality System sub-process, Document Control. This role will collaborate closely with team members supporting Records Control and Data Control, as well as broader Quality System integration activities. Success in this role will require strong cross-functional collaboration across integration teams and acquired entity personnel to achieve optimal business and compliance outcomes.

Work model, sponsorship, relocation:

At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our Arden Hills, MN at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.

Your responsibilities will include:

  • Assess document control processes and systems at acquired entities and recommend integration strategies aligned with quality system requirements, regulatory expectations, and business priorities.
  • Lead and support product integration activities by defining and executing strategies for document migration and integration into Windchill.
  • Support acquired entity document control processes, as needed, to ensure business continuity and effective integration change management.
  • Implement Boston Scientific document control processes at acquired entities through hybridization and progression to Boston Scientific Quality System processes and procedures.
  • Support Records Control and Data Control integration efforts as needed, including leading implementation of Project Tracking Plan documentation.
  • Advise integration leadership on opportunities to enhance compliance and improve Quality System processes and controls at acquired entities.
  • Conduct training for acquired entity personnel on Boston Scientific document control processes and systems.
  • Support change requests and change notices across the EP/CRM Quality Integration Team, as needed.

Required qualifications:

  • Minimum Bachelor's degree in a related discipline and relevant 2 years experience within medical device quality or a related discipline.
  • Strong understanding of medical device Quality System directives, regulations, and standards.
  • Proven experience working in regulated industries, including FDA, ISO standards, EU MDR, and ISO 13485 requirements.
  • Strong subject matter expertise and working knowledge of the Windchill application.
  • Proven experience with additional PDM/PLM systems such as Grand Avenue, MasterControl, ETQ, or similar platforms.
  • Proven experience integrating acquired entities into the Boston Scientific Quality System.
  • Demonstrated ability to collaborate effectively within a team environment.
  • Ability to travel as required, estimated at 10%.

Preferred qualifications:

  • Project management knowledge and/or experience.
  • Strong analytical, problem-solving, and communication skills.
  • High degree of integrity, professionalism, and ability to effectively influence others.

Requisition ID: 628184

Minimum Salary: $71500 

Maximum Salary: $135800 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status.  Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment.  Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements.   As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.


What Boston Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom