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Senior Biomedical Engineer Jobs in Humacao, PR (NOW HIRING)

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:

ECHO Consulting Group

Sr Data Scientist

Juncos, PR · On-site

$85 - $120/hr

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

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Senior Biomedical Engineer information

See Humacao, PR salary details

$60.2K

$128.1K

$185.8K

How much do senior biomedical engineer jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior biomedical engineer in Humacao, PR is $128,137.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,800.00 and $145,300.00 per year, depending on experience, location, and employer.

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.

Senior Biomedical Engineer jobs near you
Infographic showing various Senior Biomedical Engineer job openings in Humacao, PR as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $128,137 per year, or $61.6 per hour.

ZL01-072126 Process Development Sr Scientist

Validation & Engineering Group, Inc.

Juncos, PR • On-site

$89K - $121K/yr

Full-time

Re-posted 17 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethical standards for the following position:
  • Process Development Sr Scientist

Education :
  • Doctorate (PhD, PharmD, or MD) with relevant postdoctoral experience where applicable; or
  • Master's degree with 3+ years of relevant scientific experience; or
  • Bachelor's degree with 5+ years of relevant scientific experience.

  • A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess Engineering, Pharmaceutical Sciences, Biotechnology, Biology, Microbiology, or a related scientific discipline is highly preferred.

Attributes :
  • Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.
  • Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.
  • Experience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.
  • Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategy, and pharmaceutical quality systems.
  • Experience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.
  • Ability to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.
  • Experience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.
  • Strong technical writing, communication, presentation, and project management skills.
  • Ability to independently manage multiple projects in a fast-paced manufacturing environment while supporting commercial readiness and continuous process improvement.
  • Experience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable.

SUMMARY
To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects. Interprets experimental strategies or leads these activities. Provides input to new processes to generate robust and reliable data. Functions as a lead scientific / technical resource or as a project leader.
FUNCTIONS
1. Independently monitors or conducts experiments, studies, or a series of experiments/studies to advance projects or technologies
2. Provides advanced data analysis and interpretation, and assesses impact of data on the project and makes recommendations
3. Expands knowledge-seeking beyond core area of expertise
4. Identifies relevant external competitive knowledge
5. Independently prepares new and novel protocols/experimental design
6. Key contributor to an independent research/project team
7. Initiates productive collaborations outside of the department or company
8. Introduces new or advanced technologies and/or concepts
9. May contribute to scientific journal articles or complex technical documents as lead author
10. Leads department-wide support efforts such as safety, recruiting and committees
11. Develops supervisory and mentoring skills
12. Makes proactive decisions that contribute to the achievement of milestones
13. Plans detailed procedures for defined projects, including timelines, milestones, methodological approaches, expected results and necessary resources.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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