Quality Inspector

Pharmatech, Inc.

Quality Inspector

Lindon, UT
Full Time
Paid
  • Responsibilities

    1. JOB SUMMARY

    1. Receiving inspectors work in manufacturing environments where they complete the following tasks: inspect parts and materials, identify defects, verify whether products meet standards.

    2. They are responsible for creating and performing tests, identifying errors, and providing feedback to verify that a final product meets the quality requirements documented in the batch record. Ensures control during the production process.

    2. DUTIES & RESPONSIBILITIES

    Collect, prepare, inspect, sample, process, and document all raw materials to be transferred to the quality control lab and stored.

    Create and place expiration date labels on all raw materials.

    Ensure all raw materials have declared allergens and enforce the Allergen Management Program.

    Attend meetings required by quality management.

    Deliver daily reports on management status.

    The quality control inspector will perform cleaning inspections according to current procedures.

    Perform required testing. ( Allergens , Gluten Free, ATP, Environmental)

    Ensure GMP standards by supporting the company in the associated reports.

    Is responsible for ensuring frequent inspections according to the procedures and standards of our HCCA.

    Fill out records according to good documentation practices.

    The inspector will be responsible for verifying the scales and the quality of the products before they leave our facilities with the frequencies defined in the Batch records.

    Ensure samples required during production, for shipment to the laboratory, retentions and/or clients

    **3. EDUCATION & EXPERIENCE **

    High school diploma or equivalent.

    Experience in quality control or similar roles in the food or dietary supplement industry.

    Proficiency in using scales, PG meters, density meters, and other instruments for quality control monitoring.

    **4. SKILLS & ABILITIES **

    Knowledge and understanding of GMP standards.

    Understanding of contamination risks. Attention to detail.

    Clearly recording inspections on company-approved forms.

    Recording situations that may affect the integrity of the production process.

    Dexterity, physical strength and physical endurance, ability to move pallets, lift materials

    Preferably bilingual (English – Spanish)

    **
    **

    5. SOP’S & TRAINING

    1. 503 Deviation - Reprocessing Report

    2. 546 Collection of Customer/Laboratory Samples

    3. 509 Non-Conformances, Corrective and Preventive Action (CAPA)

    4. 300 Receiving of raw material, components, and finished goods

    5. 501 Personnel (cGMP)

    6. 522 Batch Production Records

    7. 547 Sampling Bubble Cleaning

    8. SSOP-002 Liquids Weigh Up Room Cleaning

    9. SSOP-004 Liquids Compounding Room 1

    10. SSOP-010 Liquid Production Drain Cleaning

    11. SSOP-013 Trash Bin Cleaning

    12. SSOP-014 Utensil Cleaning

    13. Others that are required and associated with the management of receipt of materials.

    6.0 WORKING CONDITIONS

    WORK ENVIRONMENT/

    PHYSICAL DEMANDS While performing the duties of this job, the employee is required to sit, stand, and lift and move objects weighing up to 50 pounds on a regular basis.

    Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus.

    Will be using a computer during your workday.