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Quality Control Sample Technician

Date: Feb 16, 2021

Location: West Haven, CT, US, 06516

Company: Glanbia

Quality Control Sample Clerk

 

POSITION PURPOSE: 

  • Works in the Quality Control Department logging raw material samples and production samples.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:

    • Logs in all raw material samples, inspects sample as specified in lab assay report, and makes notes.
    • Logs in all production samples, inspects sample as specified in lab assay report, and makes notes.
    • Prepares appropriate laboratory assay package detailing the analytical work for QC lab including a copy of the batch sheet, weighing tape log, label and outside assay paperwork. Forward the package to lab.
    • Composites multiple samples and coordinates the mailing to outside laboratories as specified in lab assay report
    • Log all raw materials and production samples in NAV.
    • Organizes the weekly storage bins for all incoming samples including those that are archived.
    • Makes folders for new products.
    • Boxes and records samples for storage and future sample retrieving.
    • Moves sample boxes to staging and or storage area.
    • Checks temperature of the ovens and records the temperature.
    • Files batch sheets, makes folders, and at the end of the year archives the batch sheets.
    • Comply with Current Good Manufacturing Procedures and Good Laboratory Practices for all laboratory tests.
    • Ability to work in a fast turnaround laboratory environment.
    • Notifies proper personnel of non-compliance.
    • Completes additional tasks and projects as assigned by management.

 

EDUCATION AND EXPERIENCE:

  • Minimum education: High School degree or GED.
  • Minimum experience:  0-2 years related work experience in food, dietary supplements, pharmaceutical or related industry.  This could be internship/student work experience.

 

JOB KNOWLEDGE, SKILLS AND ABILITIES:

  • General Knowledge of the nutritional food manufacturing process.
  • Ability to work with all levels of employees in a productive manner.
  • Working knowledge of cGMP and GLP regulations helpful.
  • Must be able to complete forms and write in a legible manner.
  • Ability to multi-task and bring tasks to completion.
  • Must be computer literate and able to learn how to use the company’s computer system.
  • Must be able to speak, read and write English fluently.
  • Must have good attention to detail.

 

SUPERVISORY RESPONSIBILITIES:

  • None

 

TRAINING REQUIREMENTS:

  • Sexual Harassment Prevention.
  • SOPs as required.
  • Lab Safety.
  • On going cGMP and GLP training to stay current with all areas required by the company.
  • Any other recommended/required training.

 

PHYSICAL REQUIREMENTS:

  • Regularly required to sit, stand, reach, bend, kneel, stoop, crouch, and walk about the building.
  • May be required to push and or pull carts with wheels containing product being moved about the building.
  • Medium physical effort required.
  • Continuous mental and visual attention required.
  • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
  • Light to Moderate physical effort required.
  • Must be able to lift 55lbs approximately every 2 weeks or more frequently as needed.
  • Fine manual motor dexterity required to complete forms, other paperwork and to perform computer data entry.

 

 

PERSONAL PROTECTIVE EQUIPMENT:

  • Lab coats as required.
  • Safety Glasses as required.
  • Gloves as required.
  • “Dust” masks as needed/required.
  • Any other PPE as required/recommended.

 

WORK ENVIRONMENT:

  • Works in a climate controlled laboratory.

 

OTHER:

  • Will be required to perform other duties as requested, directed or assigned.


Nearest Major Market: New Haven
Nearest Secondary Market: Hartford