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

Integra LifeSciences

Director, Quality Microbiology

Anasco, PR

$166K - $228K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Contamination control systems (monitoring, gowning, aseptic techniques, cleaning, etc.) The ... Create and sustain long-term strategies and advise a team of managers and scientists across the ...

TELEVICENTRO OF PUERTO RICO

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 ...

Integra LifeSciences

Manufacturing Operator I -Lyo

Anasco, PR · On-site

$17.25 - $20.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Integra LifeSciences

Manufacturing Operator I -Lyo

Anasco, PR · On-site

$17.25 - $20.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

FITS LLC

Quality Specialist

Juncos, PR · On-site

Project Management skills. * Shift: Administrative shift, and according to business needs ... Technical Writing, Quality Systems (Deviations, Change Control) and Maintenance (PM, Work Orders ...

FITS LLC

Specialist Quality Assurance

Juncos, PR · On-site

Project Management skills. * Shift: Administrative shift, and according to business needs ... Picture yourself in a lab... with all the equipment you need to put your multitasking, scientific ...

FITS LLC

Change Control Specialist

Juncos, PR · On-site

For Manufacturing Services in the Quality Systems area. WHAT MAKES YOU A FIT: The Technical Part ... Project Management skills. * Shift: Administrative and according to business needs. * Experience in:

EssilorLuxottica

Lab Technician

San Juan, PR · On-site

$12.25 - $16.50/hr

  • Medical

  • Vision

  • Life

  • Retirement

  • PTO

Because quality care helps us see the joy in life. Because learning from the best, makes us all ... Keeps management informed of potential safety opportunities (i.e. broken tiles, equipment, etc.

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Showing results 21-40

All JobsQuality Control Lab JobsQuality Control Lab Manager JobsQuality Control Lab Manager Jobs in Puerto Rico

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 are the key skills and qualifications needed to thrive as a quality control lab manager?

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 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 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 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:

Quality Control Lab Manager jobs near you

JT619 - SPECIALIST QA

Quality Consulting Group

Juncos, PR • On-site

Contractor

Posted 6 days ago

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
  • Review, approve, and maintain manufacturing process documentation (MPs) in compliance with cGMP requirements
  • Review, approve, and ensure accuracy, completeness, and traceability of GMP documentation, including protocols, reports, investigations, and quality records
  • Approve process validation protocols and reports, including PPQs and cleaning validation documentation
  • Participate as Quality representative on incident triage teams, ensuring timely and compliant decision-making
  • Review and approve planned incidents, deviations, and nonconformances, ensuring appropriate risk assessment and documentation
  • Approve Environmental Characterization and environmental monitoring reports
  • Release and maintain compliance of sanitary utility systems
  • Represent Quality Assurance on New Product Introduction (NPI) teams
  • Lead and document investigations, root cause analyses, and CAPA development
  • Lead and support site audits, including internal, external, and regulatory inspections
  • Own, maintain, and continuously improve site quality program procedures
  • Serve as QA Manager designee on the local Change Control Review Board (CCRB)
  • Review and approve risk assessments and mitigation strategies
  • Support automation systems, including review of validation and change documentation
  • Support facilities, utilities, and environmental compliance programs

Qualifications:
  • Possess a BS in Science, Engineering, Physics, Biology, Chemistry or related fields.
  • Experienced working in biopharmaveutical industry, quality organization supporting deviations, validation reports, qualifications, investigations.
  • 5 years of experienced in a highly regulated environment.
  • Experience in Quality and Compliance, experience with validation protocols and reports for clean utilities, manufacturing processes, cleaning processes, equipment, computerized systems, change control records, deviations, etc.
  • Experience in biological processes
  • Strong knowledge and hands-on experience with Aseptic manufacturing processes
  • Change Control Experience
  • Proven experience with NPI, Change Control, FATs, Validation, PPQs, and Cleaning Validation
  • Manufacturing and laboratory experience required
  • Demonstrated expertise in GMP documentation practices, including protocol/report review, investigations, and regulatory submissions
  • Strong understanding of manufacturing, distribution, QA/QC/QAL, validation, and process development activities
  • 8hrs Monday to Friday (Administrative), available nonstandard as needed.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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