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Food Industry Quality Control Jobs in Puerto Rico

PR

$17/hr

How about this one? We're seeking a Associate Quality Control - Incoming to work with one of out top biotechnology industry client at the East area of PR. With us, it's all about finding the job that ...

PR

$22 - $27/hr

What We Are Looking For The Quality Control Inspector (Construction) ensures that all civil construction activities meet contractual, regulatory, and industry standards. This role sits within the ...

PR · On-site

$90K - $110K/yr

Five or more years combined experience (or equivalent) in commercial construction industry as a Superintendent, QC Manager, Project Manager, or Project Engineer required, as well as two years ...

Sr Quality Engineer

Humacao, PR · On-site

$89K - $121K/yr

... industry. * Quality systems: Working knowledge of quality system expectations, including documentation, nonconformance handling, corrective and preventive actions, change control, and audit readiness.

This role combines quality control activities (40%), compliance monitoring (30%), documentation ... industry standards, and customer specifications while maintaining comprehensive documentation of ...

New

Strong background in Quality/ QC within the Pharmaceutical and/ or Biotechnology industry. * Excellent oral and written communication skills required with the capability of clearly presenting and ...

... industry environments. * Strong experience in business administration, financial management ... Kaizen, Quality Control, or Food Safety. * Transformational leadership and strong results ...

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Food Industry Quality Control information

What is a food industry quality control?

A Food Industry Quality Control job involves ensuring that food products meet safety, quality, and regulatory standards. Professionals in this role inspect raw materials, monitor production processes, conduct tests, and document compliance with industry regulations. They identify and address potential contamination issues, enforce sanitation protocols, and collaborate with production teams to improve quality standards. This role is essential for maintaining consumer safety and brand reputation.

What does a food industry quality control do?

In Food Industry Quality Control, your daily tasks may include conducting routine inspections, performing laboratory tests on samples, and documenting results to ensure products meet established safety and quality standards. You will frequently monitor production lines, check compliance with sanitation protocols, and investigate any deviations from procedures. Collaboration with production staff, supervisors, and regulatory bodies is common, as you'll be responsible for addressing quality concerns in real-time. This role often requires a mix of hands-on work in manufacturing or lab settings and thorough, detailed reporting.

What are the key skills and qualifications needed to thrive in food industry quality control, and why are they important?

To thrive in Food Industry Quality Control, you need an in-depth understanding of food safety regulations, laboratory testing procedures, and keen attention to detail, often backed by a degree in food science or a related field. Familiarity with quality management systems (such as HACCP or ISO 22000), laboratory equipment, and data analysis software is crucial. Strong observational skills, problem-solving abilities, and effective communication help you collaborate with various departments and address issues quickly. These competencies are vital to ensuring products consistently meet safety standards and maintaining a company's reputation for quality.

What are popular job titles related to Food Industry Quality Control jobs in Puerto Rico?

For Food Industry Quality Control jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Food Industry Quality Control jobs in Puerto Rico look for?

The top searched job categories for Food Industry Quality Control jobs in Puerto Rico are:

Infographic showing various Food Industry Quality Control job openings in Puerto Rico as of August 2026, with employment types broken down into 83% Full Time, 10% Part Time, 2% Temporary, and 5% Contract. Highlights an 100% In-person job distribution.

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.