ZipRecruiter

Log In

2

Remote Director Engineering Medical Device Jobs in Boca Raton, FL

Varsity Tutors

Biomedical Engineering Tutor

Sunrise, FL · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Miramar, FL · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Invisaclaim

Be Seen First

Medical Software Sales Representative

Boca Raton, FL · Remote

... medical device sales strongly preferred * Comfortable calling on physician practices and speaking credibly to billing and revenue cycle staff * Self-directed -- this is a commission-only role for ...

Posted today

Invisaclaim

Be Seen First

Medical Software Sales Representative

Boca Raton, FL · Remote

... medical device sales strongly preferred * Comfortable calling on physician practices and speaking credibly to billing and revenue cycle staff * Self-directed -- this is a commission-only role for ...

Posted today

next page

Showing results 1-20

All JobsEngineering Medical Device JobsRemote Director Engineering Medical Device JobsRemote Director Engineering Medical Device Jobs in Boca Raton, FL

Remote Director Engineering Medical Device information

See Boca Raton, FL salary details

$69.3K

$184.8K

$241K

How much do remote director engineering medical device jobs pay per year?

As of Sep 2, 2026, the average yearly pay for remote director engineering medical device in Boca Raton, FL is $184,772.00, according to ZipRecruiter salary data. Most workers in this role earn between $134,300.00 and $240,100.00 per year, depending on experience, location, and employer.

What does a remote director engineering medical device do?

A Remote Director of Engineering in the medical device industry oversees engineering teams and projects related to the design, development, and manufacturing of medical devices, all while working remotely. They ensure that products meet regulatory standards, manage cross-functional teams, and drive innovation from concept through to production. This role requires strong leadership, technical expertise, and experience in the medical device field, as well as excellent communication skills to coordinate with remote teams and stakeholders.

What are the key skills and qualifications needed to thrive as a remote director engineering medical device?

To thrive as a Remote Director of Engineering in Medical Devices, you need deep expertise in engineering principles, regulatory compliance (such as FDA and ISO 13485), and a relevant degree in engineering or a related field. Familiarity with product lifecycle management (PLM) systems, quality management software, and certifications like PMP or Six Sigma are highly valuable. Exceptional leadership, cross-functional communication, and strategic problem-solving skills help you effectively manage remote teams and complex projects. These capabilities ensure safe, innovative product development that complies with industry standards and drives organizational success.

What are some unique challenges faced by a remote director engineering medical device, and how can they be addressed?

A Remote Director of Engineering in the medical device field often navigates challenges such as ensuring effective collaboration across distributed teams, maintaining regulatory compliance, and overseeing complex product development cycles without onsite presence. To address these, it's important to implement robust project management tools, establish regular virtual check-ins, and foster a culture of clear documentation and accountability. Staying current with regulatory changes and leveraging digital quality management systems also help ensure that remote teams remain aligned with industry standards and deadlines.

What are popular job titles related to Remote Director Engineering Medical Device jobs in Boca Raton, FL?

For Remote Director Engineering Medical Device jobs in Boca Raton, FL, the most frequently searched job titles are:

What job categories do people searching Remote Director Engineering Medical Device jobs in Boca Raton, FL look for?

The top searched job categories for Remote Director Engineering Medical Device jobs in Boca Raton, FL are:

What cities near Boca Raton, FL are hiring for Remote Director Engineering Medical Device jobs?

Cities near Boca Raton, FL with the most Remote Director Engineering Medical Device job openings:

Remote Director Engineering Medical Device jobs near you

Quality Control Technician (Quality Engineer)

Ubertal Inc

Boca Raton, FL • Remote

Contractor

Re-posted 14 days ago

Job description

Job Title: Quality Control Technician (Quality Engineer – Contract)

Location: 100% Remote (Preferred Eastern or Central Time Zones)
Duration: 12 Months
Schedule: Full-Time, 40 Hours/Week | Standard Business Hours
Conversion: No FTE conversion available
Interview Process: 1 Round

We are seeking an experienced Quality Control Technician with strong validation and quality systems expertise to support documentation, statistical quality control, and regulatory compliance initiatives in a highly regulated pharmaceutical or manufacturing environment.

This role focuses on validation documentation, quality analysis, regulatory compliance, and cross-functional collaboration to ensure systems, products, and processes meet defined reliability and regulatory standards.

Key Responsibilities:

  • Write, review, approve, and execute validation documentation and technical reports for systems, products, and processes

  • Prepare validation protocols, test equipment, and evaluate validation data

  • Conduct statistical quality control analysis of testing results and process anomalies

  • Prepare reports summarizing study results and conformance to acceptance criteria

  • Support development and maintenance of validation programs and Standard Operating Procedures (SOPs)

  • Verify calibration, maintenance, and repair of instruments supporting Quality Systems validation

  • Participate in FMEA, RCA, and CAPA development activities

  • Ensure corrective and preventive measures meet reliability and compliance standards

  • Maintain working knowledge of FDA, CLIA, cGMP, Medical Device Directives, and other applicable regulatory standards

  • Support procedural document management and regulatory audit readiness

  • Communicate cross-functionally regarding validation studies and project deliverables

Required Qualifications:

  • Bachelor’s degree in Science, Engineering, or related field (or equivalent combination of education and relevant experience)

  • Minimum 3 years of quality/validation experience in pharmaceutical manufacturing or a highly regulated industry

  • Strong working knowledge of cGMP principles and regulatory compliance requirements

  • Experience writing and approving validation and technical documentation

  • Experience participating in FMEA, RCA, and CAPA processes

  • Strong analytical, critical thinking, and problem-solving skills

  • Project management skills with ability to manage multiple priorities and tight deadlines

  • Proficiency in Microsoft Office, statistical tools, and electronic quality systems

  • Strong written, verbal, and interpersonal communication skills

  • Ability to maintain confidentiality and demonstrate professional judgment

Preferred Qualifications:

  • ASQ Certification

  • Experience in medical device or regulated laboratory environments

This remote contract opportunity is ideal for a quality professional with deep validation experience, strong regulatory knowledge, and the ability to drive compliance and quality excellence within a regulated pharmaceutical or manufacturing environment.