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Quality Control Lab Manager Jobs in Puerto Rico (NOW HIRING)

PR · On-site

$90K - $110K/yr

Join RQ Construction as a Construction Quality Control Manager (CQCM) in Aguadilla, Puerto Rico! Join our Field Operations team and support exciting military construction projects in Aguadilla ...

The Quality Inspector will support the Construction Quality Control (CQC) plan by monitoring field ... Associate or Bachelor's degree in Civil Engineering, Construction Management, or related field.

PR

$22 - $27/hr

Project Manager or Quality Control Manager Compensation Range: $22-$27 per hour About Ceres Caribe Ceres Caribe was founded in Puerto Rico in 1998 after Hurricane Georges. It has since grown to be ...

Use computer systems (e.g., LIMS, OEFM, SAP) to manage sample testing, document results, and ... Apply to be a Associate Quality Control today! Kelly PR Offers! * Exposure to a variety of career ...

PR

$17/hr

Use computer systems (e.g., LIMS, OEFM, SAP) to manage sample testing, document results, and ... Apply to be a Associate Quality Control today! Kelly PR Offers! * Exposure to a variety of career ...

Manage quality control and assurance activities at the manufacturing site , ensuring alignment with global standards. * Lead and develop Site Quality Team members: Set quality and performance ...

PR · On-site

... C of PET radiopharmaceuticals. The position may be required to perform various radiation safety and quality related tasks as directed by management. Job Responsibilities and Duties: • Ensure ...

PR · On-site

Programming Operations Manager Functional reporting / escalation: President of Programming ... technical quality transmission of WAPA TV and all associated signals (WAPA América, digital ...

Join us in developing treatments, finding cures, and pioneering the path from lab to life while ... Expertise in JSC document management and change control processes. Johnson & Johnson is an Equal ...

Manufacturing Operator I -Lyo

Anasco, PR · On-site

$17.25 - $20.75/hr

Contact QC lab to coordinate the sampling and testing of materials. 21. Propose revisions to standard operating procedures. 22. Performs other activities as required by the supervisor. DESIRED ...

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Quality Control Lab Manager information

What does a Quality Control Lab Manager do?

A Quality Control Lab Manager oversees the daily operations of a laboratory to ensure that products meet industry and safety standards. They supervise lab staff, develop testing protocols, review test results, and maintain compliance with regulatory guidelines. The manager is also responsible for training employees, troubleshooting equipment, and implementing improvements to lab processes. Their work is crucial in guaranteeing the quality and safety of products before they reach consumers.

What is the difference between Quality Control Lab Manager vs Quality Control Technician?

AspectQuality Control Lab ManagerQuality Control Technician
CredentialsBachelor's degree in science or related field; often certifications in quality managementAssociate's or bachelor's degree; relevant technical certifications
Work EnvironmentLaboratories, overseeing testing processes and staffLaboratories, performing tests and data collection
ResponsibilitiesSupervising testing activities, managing staff, ensuring complianceConducting tests, recording results, maintaining equipment

The main difference between a Quality Control Lab Manager and a Quality Control Technician lies in their responsibilities and level of oversight. The manager oversees testing operations, manages staff, and ensures quality standards, while the technician performs the actual testing and data collection. Both roles require relevant scientific credentials and work in laboratory environments, but the manager holds a broader supervisory role.

What are some common challenges faced by a Quality Control Lab Manager, and how can they be addressed?

Quality Control Lab Managers often face challenges such as ensuring compliance with evolving regulatory standards, maintaining the accuracy and reliability of test results, and managing a diverse team of technicians. To address these issues, managers must stay updated on industry regulations, implement rigorous training programs, and foster open communication within the team. Effective use of laboratory information management systems (LIMS) and regular audits can also help maintain high-quality standards and streamline workflows.

What are the key skills and qualifications needed to thrive as a Quality Control Lab Manager, and why are they important?

To thrive as a Quality Control Lab Manager, you need a solid background in chemistry or biology, experience in laboratory operations, and often a relevant degree or certification. Familiarity with laboratory information management systems (LIMS), analytical instrumentation, and quality standards such as ISO or GMP is typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring compliance. These skills and qualities are crucial to maintain product quality, regulatory adherence, and efficient laboratory performance.
What are popular job titles related to Quality Control Lab Manager jobs in Puerto Rico? For Quality Control Lab Manager jobs in Puerto Rico, the most frequently searched job titles are:
What job categories do people searching Quality Control Lab Manager jobs in Puerto Rico look for? The top searched job categories for Quality Control Lab Manager jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Quality Control Lab Manager jobs? Cities in Puerto Rico with the most Quality Control Lab Manager job openings:

Validation Specialist - QC Equipment (CSV Focus)

Technical and Engineering Consulting

Yauco, PR • On-site

Other

Posted 26 days ago


Job description

Position Overview

Technical & Engineering Consulting is seeking a Validation Specialist with strong Computer System Validation (CSV) experience to support Quality Control (QC) laboratory equipment qualification in a regulated pharmaceutical environment.

This role will focus on analytical laboratory systems, including FTIR Spectrophotometers (Identification testing) and Endotoxin testing systems (e.g., Nebula), ensuring compliance with cGMP, Data Integrity, and regulatory expectations.

Key Responsibilities
  • Execute qualification and validation activities for QC laboratory equipment and computerized systems
  • Develop and/or support protocol generation (IQ, OQ, PQ)
  • Perform protocol execution and discrepancy resolution
  • Support review and approval of validation documentation
  • Ensure compliance with CSV lifecycle requirements (GAMP 5 approach preferred)
  • Utilize electronic document management systems (EDMS) for documentation control
  • Support data integrity assessments and audit readiness
  • Collaborate with QC, QA, IT, and Validation teams
  • Ensure alignment with QC lab requirements and regulatory standards (FDA, cGMP)
Required Qualifications
  • Bachelor's degree in Microbiology, Chemistry, Engineering, or related field
  • 3-5 years of experience in validation within regulated environments (Pharma / Biotech / Medical Devices)
  • Hands-on experience with QC laboratory equipment qualification
  • Strong knowledge of Computer System Validation (CSV)
  • Experience with analytical instrumentation (e.g., FTIR, endotoxin systems)
  • Familiarity with:
    • cGMP regulations
    • Data Integrity (ALCOA+)
    • Validation lifecycle documentation
Preferred Qualifications
  • Experience with FTIR Spectrophotometer (ID testing)
  • Experience with Endotoxin testing systems (Nebula or similar)
  • Knowledge of LIMS, Empower, or other lab systems
  • Experience with TrackWise, Kneat, or similar validation systems
  • Familiarity with GAMP 5 methodology
Key Skills
  • Strong technical writing and documentation skills
  • Attention to detail and compliance mindset
  • Ability to work cross-functionally in fast-paced environments
  • Problem-solving and analytical thinking