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Biomedical Manufacturing Jobs in Puerto Rico (NOW HIRING)

Weil Group, Inc.

Manufacturing Engineer

Dorado, PR · On-site

$64K - $82K/yr

Experience Requirements • Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. • 1-3 years in manufacturing engineering ...

Weil Group, Inc

Manufacturing Engineer

Dorado, PR · On-site

$64K - $82K/yr

Experience Requirements • Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. • 1-3 years in manufacturing engineering ...

Inteldot

Manufacturing Engineer

Dorado, PR · On-site

$64K - $82K/yr

Bachelor's degree in mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or a related engineering discipline. * One to three years of experience in Manufacturing Engineering ...

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.

Weil Group, Inc.

Senior Manufacturing Engineer

Dorado, PR · On-site +1

$80K - $109K/yr

Experience Requirements • Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. • 5-7+ years in manufacturing engineering ...

Inteldot

Sr Manufacturing Engineer

Dorado, PR · On-site

$80K - $109K/yr

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 ...

Weil Group, Inc

Senior Manufacturing Engineer

Dorado, PR · On-site

$80K - $109K/yr

Experience Requirements • Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. • 5-7+ years in manufacturing engineering ...

FITS LLC

Process Engineer I

Humacao, PR · On-site

For Engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree in Mechanical, Biomedical, Industrial or Chemical Engineering and three (3) years of ...

FITS LLC

Quality Engineer I

Humacao, PR · On-site

$72K - $93K/yr

For engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: * Bachelor's Degree in Mechanical, Biomedical, Industrial or Chemical Engineering, and three (3) years of ...

Inteldot

Process Development Sr Scientist

Juncos, PR · On-site

$89K - $121K/yr

Job Requirements: * Experience supporting sterile drug product manufacturing within the ... A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess ...

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

Validation & Engineering Group, Inc

PR

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

Validation & Engineering Group, Inc

PR · On-site

Bachelor's degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related engineering discipline). * Advanced technical background in pharmaceutical manufacturing, process ...

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Showing results 1-20

All JobsBiomedical Manufacturing JobsBiomedical Manufacturing Jobs in Puerto Rico

Biomedical Manufacturing information

What is the difference between Biomedical Manufacturing vs Medical Device Assembly?

AspectBiomedical ManufacturingMedical Device Assembly
Required CredentialsHigh school diploma or equivalent; certifications varyHigh school diploma or equivalent; often similar certifications
Work EnvironmentFactories, cleanrooms, laboratoriesFactories, cleanrooms, laboratories
Employer & Industry UsageBiotech firms, pharmaceutical companies, medical device manufacturersMedical device companies, healthcare equipment manufacturers
Common Search & Comparison IntentUnderstanding roles in biomedical manufacturingDifferences between assembly roles in medical device production

Biomedical Manufacturing involves the production of a wide range of medical products, including drugs, biologics, and devices, often requiring specialized equipment and processes. Medical Device Assembly specifically focuses on assembling medical devices, emphasizing precision and quality control. While both roles share similar environments and credentials, Biomedical Manufacturing covers a broader scope, whereas Medical Device Assembly is more specialized in device construction.

What are some common challenges faced in a biomedical manufacturing role, and how can new employees prepare for them?

In biomedical manufacturing, one common challenge is adhering to strict regulatory standards and quality control protocols, such as Good Manufacturing Practices (GMP). New employees may also find the need for meticulous documentation and routine audits demanding. To prepare, it's helpful to familiarize yourself with industry regulations and standard operating procedures, and to develop strong attention to detail. Additionally, being comfortable working both independently and as part of a cross-functional team will help you adapt to the collaborative nature of most biomedical manufacturing environments.

What is biomedical manufacturing?

Biomedical manufacturing is the process of producing medical devices, equipment, and components used in healthcare and life sciences. This field combines engineering, biology, and manufacturing principles to create products like implants, diagnostic tools, prosthetics, and surgical instruments. The process often involves strict regulatory standards to ensure safety and efficacy. Biomedical manufacturing plays a crucial role in advancing medical technology and improving patient care.

What are the key skills and qualifications needed to thrive in Biomedical Manufacturing, and why are they important?

To thrive in Biomedical Manufacturing, you need a solid background in biomedical engineering or life sciences, with knowledge of manufacturing processes and regulatory standards like GMP. Familiarity with laboratory equipment, quality control systems, and software such as CAD or ERP is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These competencies ensure the safe, efficient, and compliant production of biomedical products that meet industry and patient needs.
What job categories do people searching Biomedical Manufacturing jobs in Puerto Rico look for? The top searched job categories for Biomedical Manufacturing jobs in Puerto Rico are:
Biomedical Manufacturing jobs near you
Infographic showing various Biomedical Manufacturing job openings in Puerto Rico as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.
Manufacturing Engineer

Manufacturing Engineer

Weil Group, Inc.

Dorado, PR • On-site

$64K - $82K/yr

Full-time

Posted 12 days ago

Job description

Role Summary
The Manufacturing Engineer supports enterprise manufacturing operations by assisting with validation activities, documentation generation, manufacturing instructions, data analysis, and process improvement initiatives under the guidance of senior engineering and cross-functional team members.
Key Responsibilities
•Support IQ/OQ/PQ and process performance qualification activities by assisting with validation protocols, reports, test execution, and related documentation.
•Assist in developing in-process and receiving inspection systems, basic control plans, sampling plans, and inspection methods for components and manufacturing processes.
•Generate and maintain equipment documentation, PM/calibration procedures, manufacturing instructions, and process documentation with guidance from senior engineers.
•Support enterprise manufacturing projects from concept through implementation; participate in cross-functional collaboration with Manufacturing, Quality, R&D, Regulatory, and Supply Chain as applicable.
•Apply basic DOE, FMEA/PFMEA, risk analysis, SPC, and root-cause tools to support process characterization, optimization, and improvement.
•Support Lean Manufacturing and continuous improvement activities focused on yield, cycle time, cost, throughput, and process documentation improvements.
•Support manufacturing technologies such as laser welding, heat bonding, injection molding, vision systems, fixtures, tooling, test methods, automation, and equipment qualification under technical supervision.
•Assist with CAPA, nonconformance investigations, change control, and product/process scale-up activities as assigned.
Experience Requirements
•Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field.
•1-3 years in manufacturing engineering, process engineering, quality engineering, validation, or related technical experience within an FDA-regulated environment preferred.
•Basic working knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices used in regulated manufacturing environments preferred.
•Electrical, mechanical, industrial, or biomedical engineering background applicable to manufacturing systems.
•Exposure to automation/controls, tooling, fixtures, test methods, equipment qualification, or process validation preferred.
•Familiarity with DOE, FMEA/PFMEA, CAPA, root-cause investigation, SPC, and process capability concepts.
•Experience with Microsoft Excel and exposure to Minitab, JMP, or equivalent statistical tools preferred.
•Exposure to Lean Manufacturing, Six Sigma, Kaizen, or other continuous improvement methodologies preferred.
•Exposure to product introductions, process scale-up, design transfer, or improvements to existing processes preferred.
•Strong analytical, communication, teamwork, technical writing, and problem-solving skills.
Quality Expectations
Demonstrates commitment to patient safety and product quality by complying with all applicable quality procedures.
Ensures proper documentation discipline and supports Quality System compliance with guidance from senior engineers and quality partners.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*

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