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Director Laboratory Operations Jobs in Puerto Rico

Pinnaql

Sr Engineer

Humacao, PR · On-site

$105K - $145K/yr

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

Pinnaql

Sr Engineer

Manati, PR · On-site

$88K - $121K/yr

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

Pinnaql

Sr Engineer

Juncos, PR · On-site

$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 ...

Pinnaql

Sr Engineer

Humacao, PR · On-site

$105K - $145K/yr

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

Pinnaql

Sr Engineer

Barceloneta, PR · On-site

$88K - $121K/yr

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

Validation & Engineering Group, Inc.

Sr Engineer

Humacao, PR · On-site

$105K - $145K/yr

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

Veg Group

Sr Engineer

Humacao, PR · On-site

$75 - $100/hr

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

Validation & Engineering Group, Inc.

Sr Engineer

Manati, PR · On-site

$88K - $121K/yr

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

Pinnaql

Sr Engineer

Juana Diaz, PR · On-site

$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 ...

Validation & Engineering Group, Inc.

Sr Engineer

Humacao, PR · On-site

$105K - $145K/yr

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

Saic

ZSU FT Air Traffic Control Instructor-II

Carolina, PR · On-site

$90 - $120/hr

Direct experience as a Certified Professional Controller (CPC) at the San Juan CERAP (ZSU) is ... Operational Experience with ATC simulators including scenario design for simulation platforms (e.g.

New

Veg Group

Engineer

Juncos, PR · On-site

$60 - $80/hr

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Operations Engineering: * Function as a technical expert to equipment or systems regarding ...

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Director Laboratory Operations information

What is a director laboratory operations?

A Director of Laboratory Operations oversees the daily functions, strategic planning, and overall efficiency of a laboratory. They are responsible for ensuring compliance with regulations, managing budgets, and coordinating staff to maintain high-quality standards. This role often involves optimizing workflows, implementing new technologies, and collaborating with leadership to support research or clinical objectives. Strong leadership, problem-solving, and laboratory management experience are essential for success in this position.

What are the typical career advancement opportunities for someone in a director laboratory operations role?

A Director Laboratory Operations can pursue advancement to executive roles such as Vice President of Laboratory Services, Chief Operating Officer, or even Chief Scientific Officer, depending on the organization’s structure. This role provides valuable leadership experience and exposure to high-level strategy, budgeting, and cross-departmental collaboration. Many directors also expand their expertise by leading larger teams, overseeing multiple laboratory sites, or participating in organizational growth initiatives. Continued professional development and success in this position often open doors to significant influence on company direction and industry innovation.

What are the key skills and qualifications needed to thrive in the director laboratory operations position, and why are they important?

To excel as a Director Laboratory Operations, you need strong leadership abilities, extensive experience in laboratory management, and an advanced degree in a scientific or technical field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (such as CLIA, CAP, or ISO), and safety protocols is crucial. Excellent communication, strategic thinking, and problem-solving skills distinguish top performers in this role. These competencies ensure efficient laboratory operations, regulatory adherence, and effective team leadership in a complex and fast-paced environment.

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

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

What job categories do people searching Director Laboratory Operations jobs in Puerto Rico look for?

The top searched job categories for Director Laboratory Operations jobs in Puerto Rico are:

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

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

Director Laboratory Operations jobs near you
Infographic showing various Director Laboratory Operations job openings in Puerto Rico as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution.

Sr Engineer

Pinnaql

Humacao, PR • On-site

$105K - $145K/yr

Full-time

Re-posted 28 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.

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