PR · On-site
Contract General The Project Manager will be responsible for leading and coordinating Capital ... Ability to work in office, manufacturing, laboratory, utility, and production environments.
Quick apply
PR · On-site
Contract General The Project Manager will be responsible for leading and coordinating Capital ... Ability to work in office, manufacturing, laboratory, utility, and production environments.
Quick apply
PR · On-site
Contract General The Project Manager will be responsible for leading and coordinating Capital ... Ability to work in office, manufacturing, laboratory, utility, and production environments.
The ideal candidate will bring strong laboratory expertise, scientific problem-solving skills, and ... Establish and manage timelines to ensure project deliverables are completed on schedule.
Quick apply
The ideal candidate will bring strong laboratory expertise, scientific problem-solving skills, and ... Establish and manage timelines to ensure project deliverables are completed on schedule.
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
Punta Santiago, PR · On-site
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 ...
Punta Santiago, PR · On-site
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 ...
Punta Santiago, PR · On-site
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 ...
Punta Santiago, PR · On-site
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
PR · On-site
Medical
Dental
Vision
Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Direct startup, commissioning, and qualification of critical manufacturing and laboratory equipment ...
Quick apply
PR · On-site
Medical
Dental
Vision
Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Direct startup, commissioning, and qualification of critical manufacturing and laboratory equipment ...
Juana Diaz, PR · On-site
$18.50 - $24.50/hr
Knowledge and compliance with Good Laboratory Practices (GLP) and safety knowledge and reagents management as per SDS. * Knowledge and skills in analytical equipment. * Knowledge in chemistry ...
Juana Diaz, PR · On-site
$18.50 - $24.50/hr
Knowledge and compliance with Good Laboratory Practices (GLP) and safety knowledge and reagents management as per SDS. * Knowledge and skills in analytical equipment. * Knowledge in chemistry ...
Villalba, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Villalba, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
$18.50 - $24.50/hr
Knowledge and compliance with Good Laboratory Practices (GLP) and safety knowledge and reagents management as per SDS. * Knowledge and skills in analytical equipment. * Knowledge in chemistry ...
New
$18.50 - $24.50/hr
Knowledge and compliance with Good Laboratory Practices (GLP) and safety knowledge and reagents management as per SDS. * Knowledge and skills in analytical equipment. * Knowledge in chemistry ...
New
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
Quick apply
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
Quick apply
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
Quick apply
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
Quick apply
PR · On-site
This role is fully on-site and will focus on the execution, documentation, and lifecycle management of cleaning validation activities for manufacturing equipment, utilities, and laboratory ...
Villalba, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Villalba, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Humacao, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
Humacao, PR · On-site
Minimum 6-10 years of experience managing capital projects and programs consisting of facility infrastructure & engineering projects, manufacturing construction projects, laboratory projects, and/or ...
| Aspect | Laboratory Manager | Laboratory Supervisor |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in a science or related field; often a master's or higher for advanced roles | Usually requires a bachelor's degree in a relevant science field; certifications may enhance prospects |
| Work Environment | Oversees entire laboratory operations, manages staff, budgets, and compliance | Supervises daily lab activities, ensures procedures are followed, and supports staff |
| Employer & Industry Usage | Common in research, clinical, and industrial labs | Found in similar settings, often reporting to the Laboratory Manager |
Laboratory Managers focus on overall lab operations, strategic planning, and compliance, while Laboratory Supervisors handle daily supervision and task management. Both roles require relevant science credentials and are essential for efficient lab functioning.
The most popular types of Laboratory jobs in Puerto Rico are:
For Laboratory Manager jobs in Puerto Rico, the most frequently searched job titles are:
The top searched job categories for Laboratory Manager jobs in Puerto Rico are:
Cities in Puerto Rico with the most Laboratory Manager job openings:

Contractor
Re-posted 17 days ago
Location: Manatí & Barceloneta, Puerto Rico (On Site)
Industry: Pharmaceutical Manufacturing
Position Type: Contract
General Job Description
The Project Manager will be responsible for leading and coordinating Capital Projects, Automation, Utilities, Infrastructure, and Commissioning & Qualification (C&Q) projects within pharmaceutical manufacturing environments. This role oversees project planning, execution, timelines, resource allocation, and stakeholder communication while ensuring compliance with GMP regulations and industry standards. The Project Manager will work cross-functionally with Engineering, Automation, Validation, Quality, Manufacturing, Facilities, Utilities, Construction teams, and external vendors to ensure successful project delivery.
Job Overview
We are seeking a motivated and detail-oriented Project Manager with experience supporting pharmaceutical capital projects, automation initiatives, utility systems, infrastructure improvements, and Commissioning & Qualification (C&Q) activities. The ideal candidate will possess strong leadership, communication, and organizational skills and be capable of managing multiple projects while ensuring compliance with regulatory and quality standards. This individual will play a key role in driving project execution from initiation through completion.
Main Responsibilities
• Lead and manage pharmaceutical capital, automation, utilities, infrastructure, and C&Q projects from planning through completion.
• Develop project schedules, timelines, budgets, and resource plans.
• Coordinate cross-functional teams including Engineering, Automation, Validation, Quality, Manufacturing, Facilities, Utilities, Construction, and external vendors.
• Monitor project progress and ensure milestones and deliverables are met.
• Identify project risks and develop mitigation strategies.
• Track project scope and manage changes effectively.
• Ensure compliance with GMP, FDA, and industry regulatory requirements.
• Support commissioning, qualification, validation, and startup activities for systems, equipment, facilities, and utilities.
• Manage projects involving automation systems, process control systems, utilities, facility infrastructure upgrades, and sterile manufacturing support systems.
• Facilitate project meetings and provide status updates to stakeholders and leadership.
• Maintain project documentation and ensure proper record management.
• Support continuous improvement initiatives and project execution strategies.
General Requirements
• Strong understanding of pharmaceutical manufacturing environments.
• Knowledge of Commissioning & Qualification (C&Q) lifecycle activities.
• Familiarity with GMP regulations and quality standards.
• Experience supporting capital projects, automation systems, utility systems, facility infrastructure projects, or construction activities within regulated environments.
• Knowledge of automation platforms, process control systems, Computer Systems Validation (CSV), or related technologies is preferred.
• Strong project planning and organizational skills.
• Excellent communication and stakeholder management abilities.
• Ability to prioritize multiple tasks and manage competing deadlines.
• Proficiency in Microsoft Office Suite and project management tools.
• Ability to work independently and in a team-oriented environment.
• Strong problem-solving and analytical skills.
Education
• Bachelor’s degree in Engineering, Life Sciences, Pharmaceutical Sciences, Project Management, Construction Management, or related technical field.
• Project Management certifications (PMP or similar) are a plus.
Experience
• Minimum of 3 years of experience in Project Management within pharmaceutical, biotech, medical device, or regulated manufacturing environments.
• Experience supporting Capital Projects, Automation Projects, Utilities Systems, Infrastructure Projects, Construction Projects, or Commissioning & Qualification (C&Q) activities preferred.
• Experience managing cross-functional teams and project deliverables.
• Experience working with sterile manufacturing environments, process control systems, automation platforms, utilities, or facility infrastructure projects is highly desirable.
• Knowledge of pharmaceutical processes and regulatory environments preferred.
Physical Requirements
• Ability to work in office, manufacturing, laboratory, utility, and production environments.
• Ability to stand, walk, sit, and move throughout facilities for extended periods.
• May require occasional lifting of up to 20 lbs.
• Ability to wear required Personal Protective Equipment (PPE) in manufacturing areas.
• May require occasional travel to client sites or project locations.
• Ability to access controlled manufacturing, utility, construction, and cleanroom environments as needed.