qc technician
Job
Spherion
Fort Pierce, FL (In Person)
$46,800 Salary, Full-Time
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Job Description
Job details Summary Spherion $41,600 - $52,000 per year Permanent 8:00 AM - 5:00 PM Industry manufacturing & production (Production Occupations) Reference number S_174810 Job details The QC Technician is responsible for executing all quality assurance and food safety monitoring activities during plant operations for a orange juice processing facility. This role ensures compliance with 21 CFR 117 (FSMA Preventive Controls), 21 CFR 120 (Juice HACCP), GMP standards, and the company's Quality Management System (QMS). ... The QC Technician monitors production processes, verifies Critical Control Points (CCPs), performs in-process inspections, and ensures accurate documentation of quality records.
Perform routine in-process quality checks.?Verify lot coding and labeling accuracy.?Monitor fill weights and packaging integrity.
Sampling & Testing Support?
Collect production samples according to approved sampling plans.?Deliver samples to the Laboratory Technician for analytical testing.?Performs in-line and inbound tankers Brix, acidity, pH, pulp, and other juice quality tests.?Ensure proper sample traceability and documentation.
GMP & Sanitation Monitoring?
Monitor GMP compliance during production.?Conduct pre-operational inspections as assigned.?Verify sanitation activities meet established standards.?Enforce hygiene compliance on the production floor.
Documentation & Recordkeeping?
Accurately complete production quality records.?Maintain compliance with FDA documentation requirements.?Report deviations, non-conformances, and unusual conditions immediately.?Support product hold procedures as directed.
Non-Conformance & Escalation?
Immediately notify QA Supervisor of CCP deviations, out-of-specification conditions, or food safety risks.?Assist in containment of affected product.?Participate in root cause investigations as requested.
Audit & Inspection Support?
Maintain inspection-ready documentation.?Support internal audits.?Provide records during regulatory inspections as directed by the QA Supervisor.
Authority & Limits?
Place product on temporary hold pending QA Supervisor review.?Stop production momentarily if an immediate food safety risk is observed (with immediate notification).?Does not approve final product release or communicate with regulatory authorities. experience 1-4 years skills Associate's degree in Food Science or related field preferred.
Experience in food or beverage manufacturing preferred. qualifications Qualifications?
High school diploma required?1?3 years of experience in manufacturing setting. ?Knowledge of GMP and basic HACCP principles.
Knowledge & SkillsHard Skills?
Proficiency in English (written and verbal); Spanish language skills preferred.?Basic understanding of 21 CFR 117 and 21 CFR 120 requirements.?Ability to complete detailed documentation accurately.?Computer literacy and basic ERP/data entry skills.
Soft Skills?
Strong attention to detail.?Reliable and accountable.?Team-oriented and cooperative.?Ability to work in a fast-paced production environment.?Strong communication skills. education High School share this job. send via e-mail print it
Responsibilities:
In-Process Monitoring & CCP Verification Perform routine in-process quality checks. Verify lot coding and labeling accuracy. Monitor fill weights and packaging integrity. Sampling & Testing Support Collect production samples according to approved sampling plans. Deliver samples to the Laboratory Technician for analytical testing. Performs in-line and inbound tankers Brix, acidity, pH, pulp, and other juice quality tests. Ensure proper sample traceability and documentation. GMP & Sanitation Monitoring Monitor GMP compliance during production. Conduct pre-operational inspections as assigned. Verify sanitation activities meet established standards. Enforce hygiene compliance on the production floor. Documentation & Recordkeeping Accurately complete production quality records. Maintain compliance with FDA documentation requirements. Report deviations, non-conformances, and unusual conditions immediately. Support product hold procedures as directed. Non-Conformance & Escalation Immediately notify QA Supervisor of CCP deviations, out-of-specification conditions, or food safety risks. Assist in containment of affected product. Participate in root cause investigations as requested. Audit & Inspection Support Maintain inspection-ready documentation. Support internal audits. Provide records during regulatory inspections as directed by the QA Supervisor. Authority & Limits Place product on temporary hold pending QA Supervisor review. Stop production momentarily if an immediate food safety risk is observed (with immediate notification). Does not approve final product release or communicate with regulatory authorities.Working hours:
8:00 AM - 5:00PM Skills:
Associate's degree in Food Science or related field preferred. Experience in food or beverage manufacturing preferred.Education:
High School Experience:
1-4 yearsQualifications:
Qualifications High school diploma required 1-3 years of experience in manufacturing setting. Knowledge of GMP and basic HACCP principles. Knowledge & Skills Hard Skills Proficiency in English (written and verbal); Spanish language skills preferred. Basic understanding of 21 CFR 117 and 21 CFR 120 requirements. Ability to complete detailed documentation accurately. Computer literacy and basic ERP/data entry skills. Soft Skills Strong attention to detail. Reliable and accountable. Team-oriented and cooperative. Ability to work in a fast-paced production environment. Strong communication skills. If you have the experience and skills we are looking for, APPLYTODAY AT
https://www.spherion.com/ TODAY.MUST INCLUDE DETAILED RESUME WITH AT LEAST LAST 7 YEARS OF FULL WORK EXPERIENCE
Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). Show less Show more The QC Technician is responsible for executing all quality assurance and food safety monitoring activities during plant operations for a orange juice processing facility. This role ensures compliance with 21 CFR 117 (FSMA Preventive Controls), 21 CFR 120 (Juice HACCP), GMP standards, and the company's Quality Management System (QMS). The QC Technician monitors production processes, verifies Critical Control Points (CCPs), performs in-process inspections, and ensures accurate documentation of quality records.Responsibilities:
In-Process Monitoring & CCP Verification Perform routine in-process quality checks. Verify lot coding and labeling accuracy. Monitor fill weights and packaging integrity. Sampling & Testing Support Collect production samples according to approved sampling plans. Deliver samples to the Laboratory Technician for analytical testing. Performs in-line and inbound tankers Brix, acidity, pH, pulp, and other juice quality tests. Ensure proper sample traceability and documentation. GMP & Sanitation Monitoring Monitor GMP compliance during production. Conduct pre-operational inspections as assigned. ... Verify sanitation activities meet established standards. Enforce hygiene compliance on the production floor. Documentation & Recordkeeping Accurately complete production quality records. Maintain compliance with FDA documentation requirements. Report deviations, non-conformances, and unusual conditions immediately. Support product hold procedures as directed. Non-Conformance & Escalation Immediately notify QA Supervisor of CCP deviations, out-of-specification conditions, or food safety risks. Assist in containment of affected product. Participate in root cause investigations as requested. Audit & Inspection Support Maintain inspection-ready documentation. Support internal audits. Provide records during regulatory inspections as directed by the QA Supervisor. Authority & Limits Place product on temporary hold pending QA Supervisor review. Stop production momentarily if an immediate food safety risk is observed (with immediate notification). Does not approve final product release or communicate with regulatory authorities.Working hours:
8:00 AM - 5:00PM Skills:
Associate's degree in Food Science or related field preferred. Experience in food or beverage manufacturing preferred.Education:
High School Experience:
1-4 yearsQualifications:
Qualifications High school diploma required 1-3 years of experience in manufacturing setting. Knowledge of GMP and basic HACCP principles. Knowledge & Skills Hard Skills Proficiency in English (written and verbal); Spanish language skills preferred. Basic understanding of 21 CFR 117 and 21 CFR 120 requirements. Ability to complete detailed documentation accurately. Computer literacy and basic ERP/data entry skills. Soft Skills Strong attention to detail. Reliable and accountable. Team-oriented and cooperative. Ability to work in a fast-paced production environment. Strong communication skills. If you have the experience and skills we are looking for, APPLYTODAY AT
https://www.spherion.com/ TODAY.MUST INCLUDE DETAILED RESUME WITH AT LEAST LAST 7 YEARS OF FULL WORK EXPERIENCE
Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). Show less Show more key responsibilities In-Process Monitoring & CCP Verification?Perform routine in-process quality checks.?Verify lot coding and labeling accuracy.?Monitor fill weights and packaging integrity.
Sampling & Testing Support?
Collect production samples according to approved sampling plans.?Deliver samples to the Laboratory Technician for analytical testing.?Performs in-line and inbound tankers Brix, acidity, pH, pulp, and other juice quality tests.?Ensure proper sample traceability and documentation.
GMP & Sanitation Monitoring?
Monitor GMP compliance during production.?Conduct pre-operational inspections as assigned.?Verify sanitation activities meet established standards.?Enforce hygiene compliance on the production floor.
Documentation & Recordkeeping?
Accurately complete production quality records.?Maintain compliance with FDA documentation requirements.?Report deviations, non-conformances, and unusual conditions immediately.?Support product hold procedures as directed.
Non-Conformance & Escalation?
Immediately notify QA Supervisor of CCP deviations, out-of-specification conditions, or food safety risks.?Assist in containment of affected product.?Participate in root cause investigations as requested.
Audit & Inspection Support?
Maintain inspection-ready documentation.?Support internal audits.?Provide records during regulatory inspections as directed by the QA Supervisor.
Authority & Limits?
Place product on temporary hold pending QA Supervisor review.?Stop production momentarily if an immediate food safety risk is observed (with immediate notification).?Does not approve final product release or communicate with regulatory authorities. experience 1-4 years skills Associate's degree in Food Science or related field preferred.
Experience in food or beverage manufacturing preferred. qualifications Qualifications?
High school diploma required?1?3 years of experience in manufacturing setting. ?Knowledge of GMP and basic HACCP principles.
Knowledge & SkillsHard Skills?
Proficiency in English (written and verbal); Spanish language skills preferred.?Basic understanding of 21 CFR 117 and 21 CFR 120 requirements.?Ability to complete detailed documentation accurately.?Computer literacy and basic ERP/data entry skills.
Soft Skills?
Strong attention to detail.?Reliable and accountable.?Team-oriented and cooperative.?Ability to work in a fast-paced production environment.?Strong communication skills. education High School share this job. send via e-mail print it
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