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Laboratory Director Jobs in Puerto Rico (NOW HIRING)

Sr Engineer

Juana Diaz, PR

$101K - $139K/yr

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Minimum of 4 years of experience in direct pharmaceutical, medical device or biotechnology ...

QA Formulation Lab Tech II

Juana Diaz, PR · On-site

$18.50 - $24.50/hr

Also is accountable for the use of Laboratory Instruments operative systems and equipment. Responsibilities are to be performed in compliance with good laboratory practices, QSR, PAL, ISO 13485 ...

QA Formulation Lab Tech II

Juana Diaz, PR · On-site

$18.50 - $24.50/hr

Also is accountable for the use of Laboratory Instruments operative systems and equipment. Responsibilities are to be performed in compliance with good laboratory practices, QSR, PAL, ISO 13485 ...

Transport blood samples to requested locations (i.e. hospital laboratory) with follow up on results ... as directed and supervised by Primary Transplant Coordinator and Surgical Coordinator. * Assist ...

Transport blood samples to requested locations (i.e. hospital laboratory) with follow up on results ... as directed and supervised by Primary Transplant Coordinator and Surgical Coordinator. * Assist ...

Quality - Quality Compliance Supervisor

Vega Baja, PR · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... Director for site activities. • Responsible for continuous review of FDA regulations, ISO ... laboratory submission forms, etc.), interacts with customers as needed • Support microbiology ...

Physician

Mayaguez, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Ponce, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Guayama, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

San Juan, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Comerio, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Utuado, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Arecibo, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Guaynabo, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Physician

Vieques, PR · On-site

$124K/yr

... laboratory or Director of Clinical Laboratory Medicine). * English Language Proficiency- Must be proficient in spoken and written English in accordance with 38 U.S.C. 7402(d). * Selective Placement ...

Showing results 21-40

Laboratory Director information

What is a laboratory director?

A Laboratory Director is a senior professional responsible for overseeing the operations, quality control, and regulatory compliance of a laboratory. They ensure that all laboratory procedures adhere to industry standards and legal requirements, manage staff, and develop and implement policies for efficient workflow. Laboratory Directors often have advanced degrees in laboratory science or a related field and possess extensive experience in laboratory management. Their leadership is crucial in maintaining the accuracy, reliability, and safety of laboratory results.

What does a laboratory director do?

As a laboratory director, you oversee all operations within a medical lab. Your responsibilities include completing administrative duties, managing personnel, supervising procedures, checking supplies, maintaining the equipment, and setting up the lab. Depending on your qualifications and skills, you may also assist with planning experiments and interpreting test results. It is your responsibility to ensure all staff activities and tests meet safety standards and regulations and produce quality results. A laboratory director works closely with the laboratory manager and communicates with other departments, such as human resources and clinical staff, so you need strong communication skills.

What are the key skills and qualifications needed to thrive as a laboratory director, and why are they important?

To thrive as a Laboratory Director, you need advanced knowledge in laboratory science, strong management abilities, and typically a relevant advanced degree with significant laboratory experience. Familiarity with laboratory information management systems (LIMS), quality control protocols, and certifications such as CLIA or CAP accreditation are often required. Leadership, problem-solving, and effective communication are standout soft skills for guiding teams and maintaining regulatory compliance. These skills and qualities are crucial for ensuring reliable laboratory operations, staff performance, and adherence to industry standards.

What are some common challenges faced by laboratory directors, and how can they be managed effectively?

Laboratory Directors often face challenges such as maintaining regulatory compliance, managing diverse teams, and ensuring the accuracy and timeliness of test results. Balancing administrative responsibilities with scientific oversight can be demanding, especially in high-volume or specialized labs. Effective management involves staying updated with changing regulations, fostering clear communication among staff, and implementing robust quality control processes. Building a culture of continuous improvement and professional development also helps address these challenges proactively.

What is the difference between Laboratory Director vs Laboratory Supervisor?

AspectLaboratory DirectorLaboratory Supervisor
CredentialsTypically requires a relevant advanced degree (e.g., PhD, MD) and certificationUsually requires a bachelor's or master's degree in a related field
Work EnvironmentOversees multiple labs or departments, strategic planningManages daily operations within a specific lab
ResponsibilitiesSets policies, ensures compliance, manages budgetsSupervises staff, ensures quality control, handles workflow

The Laboratory Director holds a higher-level, strategic role overseeing entire laboratories or networks, often requiring advanced credentials. The Laboratory Supervisor focuses on daily operational management within a specific lab. Both roles are essential but differ in scope, responsibilities, and required qualifications.

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

The most popular types of Laboratory jobs in Puerto Rico are:

What are popular job titles related to Laboratory Director jobs in Puerto Rico?

For Laboratory Director jobs in Puerto Rico, the most frequently searched job titles are:

What cities in Puerto Rico are hiring for Laboratory Director jobs?

Cities in Puerto Rico with the most Laboratory Director job openings:

Infographic showing various Laboratory Director job openings in Puerto Rico as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 2% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

$101K - $139K/yr

Full-time

Re-posted 25 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:

  • Sr Engineer

Description:

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.

Qualifications:

  • Engineer with years of experience, preferably in aseptic processing environments, including Fill/Finish operations such as vial and syringe filling lines.
  • Experience in characterization activities and performance qualification (PQ) for New Product Introductions (NPI).
  • Minimum of 4 years of experience in direct pharmaceutical, medical device or biotechnology industries.
  • Experience in direct process / manufacturing areas.
  • Must be fully bilingual (English / Spanish) with excellent oral skills.
  • Must be proficient using MS Windows and Microsoft Office applications.
  • Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
  • Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
  • SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT).
  • Available to work extended hours, possibility of weekends and holidays.


Education:

  • Masters + 2 years of Engineering experience OR Bachelors in Engineering + 4 years of Engineering experience. Preferred: Mechanical or Chemical Engineering


Competencies/Skills:

  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes
  • Familiarity with documentation in a highly regulated environment
  • Ability to operate specialized laboratory equipment and computers as appropriate.
  • Ability to interpret and apply GLPs and GMPs.
  • Ability to apply engineering science to production.
  • Able to develop solutions to routine technical problems of limited scope
  • Comprehensive understanding of validation protocol execution requirements.

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.