Quality Control Technician 2nd shift

Cibo Vita; Totowa (NJ); On-site; USD 38,000 - 50,000; Full time

Job summary

Cibo Vita in Totowa, New Jersey, is searching for a Quality Control Technician responsible for monitoring production lines to ensure food safety and quality standards. This role involves a variety of tasks including daily inspections, conducting audits, and maintaining records.

The ideal candidate should have GMP experience, strong communication skills, and be bilingual in Spanish and English. This position offers the opportunity to make a significant impact within the company.

Qualifications

• Experience in GMP within a manufacturing environment.
• Knowledge of safety rules and regulations.
• Basic computer skills.

Responsibilities

• Perform daily inspections and ensure quality control tests.
• Conduct GMP audits and handle HACCP records.
• Communicate nonconforming products to appropriate personnel.

Skills

GMP experience

Bilingual (Spanish/English)

Good communication skills

Attention to detail

Job description

Job Description

The Quality Control Technician will be responsible for monitoring production lines. This role offers responsibility, variety, and the satisfaction that your role makes a real impact on our success. The position will report to the Quality Control Supervisor. Ensure that all raw material and finished goods meet all quality and food safety standards.

Responsibilities

• Perform daily pre-operational inspections and closing cleaning inspections.
• Ensure that quality control tests are effectively conducted.
• Conduct daily GMP audits.
• Check label accuracy and integrity.
• Handle HACCP & SQF record keeping.
• QC Checklist.
• Label Inspection-CCP#1.
• Metal Detector Monitoring Form.
• Lot Inspection and other necessary forms.
• Conduct micro test sampling.
• Prepare customer samples.
• Conduct sensory evaluation.
• Take all measures necessary to ensure food safety.
• Calibrate equipment.
• Allergen validation testing.
• ATP testing.
• Assist in implementing corrective action required as a result of audit.
• Ensure nonconforming product is handled appropriately.
• Communicate nonconforming product to appropriate personnel.
• Follow up with the HOLD procedure.
• Other duties will be added as necessary.

Requirements

• GMP experience in manufacturing environment.
• Working knowledge of safety rules, regulations and training.
• Bilingual (Spanish/English).
• Good communication skills.
• Basic computer skills.
• Attention to detail.
• Ability to work in a team environment.