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Senior Biomedical Engineer Jobs in Puerto Rico (NOW HIRING)

Inteldot

Sr Manufacturing Engineer

Dorado, PR · On-site

$80K - $109K/yr

Employment type: Full time and onsite role Role Summary The Senior Manufacturing Engineer provides ... Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or ...

FITS LLC

PR · On-site

$89K - $121K/yr

Bachelor's Degree in Mechanical, Electrical, Industrial, Manufacturing, or Biomedical Engineering, or a related technical field, and 5-7+ years of experience in an FDA-regulated environment.

Inteldot

Manufacturing Engineer

Dorado, PR · On-site

$64K - $82K/yr

Working closely with senior engineers and cross-functional teams, this role contributes to the ... Bachelor's degree in mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or ...

QRC Group

Sr Data Scientist

Juncos, PR · On-site

$110 - $150/hr

Juncos, Puerto Rico | Posted on 08/13/2026 We are seeking Sr Data Scientist, with knowledge of ... Engineering, Biomedical Engineering, Biotechnology, Manufacturing Engineering, or a related ...

Validation & Engineering Group, Inc

PR

$89K - $122K/yr

Process Development Sr Scientist Education: * Doctorate (PhD, PharmD, or MD) with relevant ... A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess ...

FITS LLC

Sr. Quality Engineer

Juncos, PR · On-site

$86K - $117K/yr

Bachelor's Degree in Mechanical, Biomedical, Industrial or Chemical Engineering, and five (5) years of exposure within the Medical Devices Industry. * Bilingual: Spanish and English * Soft Skills:

Inteldot

Sr Data Scientist 35618

Juncos, PR · On-site

Industrial Engineering, Systems Engineering, Computer Science, Chemical Engineering, Biomedical Engineering, Biotechnology, Manufacturing Engineering, or a related technical discipline. A background ...

Inteldot

Sr Data Scientist 35618

Juncos, PR · On-site

$90 - $130/hr

Industrial Engineering, Systems Engineering, Computer Science, Chemical Engineering, Biomedical Engineering, Biotechnology, Manufacturing Engineering, or a related technical discipline. A background ...

New

CIS International LLC

PR

Industrial Engineering, Systems Engineering, Computer Science, Chemical Engineering, Biomedical Engineering, Biotechnology, Manufacturing Engineering, or a related technical discipline. * A ...

All JobsBiomedical Engineer JobsSenior Biomedical Engineer JobsSenior Biomedical Engineer Jobs in Puerto Rico

Senior Biomedical Engineer information

What is a senior biomedical engineer?

A Senior Biomedical Engineer is responsible for designing, developing, and improving medical devices, equipment, and systems used in healthcare. They collaborate with medical professionals, researchers, and regulatory teams to ensure safety, compliance, and effectiveness. This role often involves project management, troubleshooting complex biomedical issues, and mentoring junior engineers. Senior Biomedical Engineers play a key role in advancing medical technology to improve patient care and treatment outcomes.

What are the typical responsibilities of a senior biomedical engineer?

Senior Biomedical Engineers often lead the development and improvement of medical devices, oversee compliance with industry standards, and provide technical guidance to engineering teams. Their responsibilities frequently include project management, conducting risk assessments, collaborating with clinicians to understand user needs, and troubleshooting complex equipment issues. They may also be involved in training staff, managing documentation for regulatory submissions, and interacting with vendors. This combination of technical leadership and cross-functional collaboration ensures that biomedical solutions are safe, effective, and tailored to healthcare settings.

What are the key skills and qualifications needed to thrive as a senior biomedical engineer?

A Senior Biomedical Engineer requires a comprehensive understanding of biomedical engineering principles, advanced problem-solving abilities, and a bachelor's or master's degree in biomedical engineering or a related field. Familiarity with CAD software, medical device regulations (such as FDA or ISO standards), and certifications like Certified Biomedical Equipment Technician (CBET) are often essential. Strong leadership, project management, and effective communication skills help coordinate multidisciplinary teams and guide junior engineers. These skills are crucial for ensuring the safe and effective design, implementation, and maintenance of biomedical technologies in healthcare environments.

What are the most commonly searched types of Biomedical Engineer jobs in Puerto Rico?

The most popular types of Biomedical Engineer jobs in Puerto Rico are:

What are popular job titles related to Senior Biomedical Engineer jobs in Puerto Rico?

For Senior Biomedical Engineer jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Senior Biomedical Engineer jobs in Puerto Rico look for?

The top searched job categories for Senior Biomedical Engineer jobs in Puerto Rico are:

Senior Biomedical Engineer jobs near you
Infographic showing various Senior Biomedical Engineer job openings in Puerto Rico as of August 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution.

Sr Manufacturing Engineer

Inteldot

Dorado, PR • On-site

$80K - $109K/yr

Contractor

Re-posted 9 days ago

Job description

Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Employment type: Full time and onsite role
Role Summary
The Senior Manufacturing Engineer provides technical leadership for manufacturing operations by leading process validation, manufacturing process development, continuous improvement initiatives, and cross-functional engineering projects. This role works independently, drives technical solutions, and mentors junior engineers while ensuring compliance with quality and regulatory requirements.
Key Responsibilities
  • Lead equipment and process validation activities (IQ/OQ/PQ), including validation strategy, protocol development, execution, and reporting.
  • Design and implement inspection methods, control plans, sampling plans, and manufacturing quality controls.
  • Develop, review, and maintain manufacturing documentation, including work instructions, equipment procedures, preventive maintenance, calibration, and process control documentation.
  • Manage manufacturing projects from concept through implementation while collaborating with Manufacturing, Quality, R&D, Regulatory, Supply Chain, and external partners.
  • Apply engineering and quality tools such as DOE, PFMEA, SPC, MSA, risk analysis, and root cause investigations to optimize manufacturing processes.
  • Lead Lean Manufacturing and continuous improvement initiatives focused on productivity, quality, yield, throughput, process capability, and cost reduction.
  • Provide technical leadership for manufacturing technologies including automation, tooling, fixtures, vision systems, laser welding, heat bonding, injection molding, equipment qualification, and test methods.
  • Lead change controls, CAPA investigations, nonconformance investigations, process transfers, and product scale-up activities while ensuring regulatory compliance.
  • Mentor junior engineers and provide technical guidance to cross-functional teams.
Requirements
  • Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or a related engineering discipline.
  • Five to seven or more years of experience in Manufacturing Engineering, Process Engineering, Validation Engineering, or Quality Engineering within a regulated manufacturing environment.
  • Strong knowledge of FDA Quality System Regulations (21 CFR Part 820), GMP, ISO 13485, and Good Documentation Practices.
  • Experience with manufacturing automation, equipment qualification, tooling, fixtures, process validation, and manufacturing systems.
  • Proficiency with engineering and quality tools including DOE, PFMEA, CAPA, SPC, MSA, root cause analysis, and statistical analysis.
  • Experience with Minitab, JMP, or similar statistical software is preferred.
  • Knowledge of Lean Manufacturing, Six Sigma, Kaizen, Value Stream Mapping, or other continuous improvement methodologies.
  • Experience supporting new product introductions, design transfer, process scale-up, and manufacturing process optimization.
  • Strong project management, leadership, communication, technical writing, analytical, and problem-solving skills.
Quality Expectations
  • Ensure compliance with all applicable quality procedures, regulatory requirements, and documentation standards.
  • Promote a culture of product quality, patient safety, and continuous improvement while providing technical leadership across engineering and manufacturing teams.

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