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Biomedical Manufacturing Jobs in Puerto Rico (NOW HIRING)

... Civil, Biomedical, or related engineering discipline). * 5-10 years of project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing ...

PR · On-site

... Civil, Biomedical, or related engineering discipline). * 5-10 years of project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing ...

PR · On-site

... Civil, Biomedical, or related engineering discipline). * 5-10 years of project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing ...

Biomedical Engineering Job Category: Scientific/Technology All Job Posting Locations: Anasco ... Implementation of cost-effective manufacturing solutions to drive end-to-end manufacturing ...

Kelly ® Engineering is seeking Staff Engineer for contract position at manufacturing client in ... S. engineering (mechanical, electrical, biomedical and or chemical industrial) Excellent analytical ...

Provides Design for Manufacturability (DFM) input to the engineering print package. * Contributes ... Mechanical or Biomedical Engineer preferred. * Experience leading complex projects. * Knowledge in ...

Provides Design for Manufacturability (DFM) input to the engineering print package. * Contributes ... Mechanical or Biomedical Engineer preferred. * Experience leading complex projects. * Knowledge in ...

Provides Design for Manufacturability (DFM) input to the engineering print package. * Contributes ... Mechanical or Biomedical Engineer preferred. * Experience leading complex projects. * Knowledge in ...

PR · On-site

... manufacturer specifications. Coordinate preventive maintenance (PM) with clients and schedule in ... Southeastern Biomedical: i. Request certification quotes. ii. Submit for approval. iii. Coordinate ...

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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:
Infographic showing various Biomedical Manufacturing job openings in Puerto Rico as of June 2026, with employment types broken down into 1% As Needed, 38% Full Time, 45% Part Time, 1% Contract, and 15% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution.

Full-time

Posted 21 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 ethics standards for the following position:

  • Project Manager

Description:

We are seeking a Project Manager to lead and coordinate capital, engineering, manufacturing, quality, validation, automation, and operational improvement projects within a regulated pharmaceutical, biotechnology, or medical device environment.

The Project Manager will be responsible for planning, executing, monitoring, and closing projects while ensuring alignment with scope, schedule, budget, quality, and compliance requirements. This individual will serve as the primary point of coordination among cross-functional stakeholders and will drive project execution from initiation through completion.

Key Responsibilities

  • Manage multiple projects simultaneously, ensuring adherence to project scope, schedule, budget, and quality objectives.
  • Develop and maintain project plans, schedules, resource forecasts, risk registers, and status reports.
  • Coordinate activities among Engineering, Manufacturing, Quality, Validation, Automation, Supply Chain, and other functional teams.
  • Facilitate project meetings and communicate project status, risks, issues, and mitigation plans to stakeholders and leadership.
  • Monitor project performance using established KPIs and project management best practices.
  • Support capital project execution, equipment implementation, facility upgrades, process improvements, technology transfers, and operational initiatives.
  • Identify and proactively manage project risks, issues, and dependencies.
  • Ensure project documentation is complete, accurate, and compliant with applicable procedures and regulatory requirements.
  • Drive accountability among team members and support timely decision-making.
  • Support vendor management, contractor coordination, and procurement activities as required.
  • Promote a culture of safety, quality, compliance, and continuous improvement.

Qualifications

  • Bachelor’s Degree in Engineering (Mechanical, Chemical, Electrical, Industrial, Civil, Biomedical, or related engineering discipline).
  • 5–10 years of project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.
  • Experience managing engineering, capital, manufacturing, quality, validation, automation, or operational excellence projects.
  • Demonstrated experience leading cross-functional teams and coordinating multiple stakeholders.
  • Strong understanding of project planning, scheduling, budgeting, forecasting, and risk management.
  • Excellent verbal and written communication skills, with the ability to effectively interact with technical teams, management, and clients.
  • Proficiency with Microsoft Project, Smartsheet, Primavera P6, or equivalent project management tools.

Preferred

  • PMP certification.
  • Experience supporting GMP-regulated environments.
  • Experience managing capital projects, facility expansions, equipment installations, CQV programs, process improvements, or technology transfers.
  • Familiarity with FDA regulations, cGMP requirements, and life sciences industry standards.

Soft Skills

  • Strong leadership and organizational skills.
  • Excellent interpersonal and stakeholder management abilities.
  • High emotional intelligence and professional maturity.
  • Strong problem-solving and decision-making capabilities.
  • Ability to influence and drive results without direct authority.
  • Self-motivated, proactive, and highly accountable.
  • Ability to work effectively in a fast-paced, matrixed environment.

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.