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QC Line Inspector in Culver City, CA at Volt

Date Posted: 3/14/2019

Job Snapshot

  • Employee Type:
    Contingent
  • Job Type:
  • Duration:
    24 weeks
  • Date Posted:
    3/14/2019
  • Job ID:
    157378
  • Contact Name
    Volt Branch
  • Phone
    310-316-8523

Job Description

* For IMMEDIATE consideration please email your resume to kbonilla@volt.com or contact VOLT and ask for Kathryn Bonilla at 562-384-5327 for more information about this position. *


I have a Tempt-to- Hire position for a QC Line Inspector that we are looking to hire IMMEDIATELY for a Personal Care Product manufacturing company. Below is the description:

Job Description:
Job Title: QC Line Inspector

 City: Culver city- relocating to Bell, CA
State: California
Job Duration: Temp-to-hire
Full-Time/Part-Time: Full-Time / Hourly
Schedule: M-F Must be flexible to OT and possible weekends
Pay Rate: $16/hr

Job Description

Basic Purpose

Perform finished product inspection to ensure products distributed to customer meet specifications. Functions include but not limited to: Inspect production line before start of production; Inspect finished products; Approve production set-up; Verify information on the batch records; Provide assistance to Production for self-inspection; Prepare and file batch records; Maintain Finished Product Standards; Perform any other functions requested by any Quality Department Supervisor.

Responsibilities

  • Prepare product standards with proper information and submit to lead/supervisor for approval. After new revision is approved, remove previous product standard from the cabinet.
  • Verify components used on each filing line are labeled properly
  • Perform production line in-process inspections in accordance with current specifications. Record inspection result on Finished Product Inspection in a timely manner ( at the time is being performed, no back dated information is allowed)
  • Submit Component Reconciliation and Yield (F084) for OTC products immediately after each product is completed.
  • Monitor and verify calibration of equipment used to test or inspect materials; any equipment issue must be reported to immediate supervisor in a timely manner.
  • Pull QC approved retains, validation and stability samples as required.
  • File documentation and production batch records
  • Enter retain samples information into the retain samples log and maintain retain samples (each work order must have its own retain sample)
  • Record any unusual incident in comment section for each component during finished product inspection.
  • Initiate a QA HOLD, if product fails to meets requirements
  • Prepare and check the batch record to ensure all required documents are completed
  • Submit batch record to QA Lead for review within 24 hours of work order completion
  • Other duties and responsibilities as may be required by immediate supervisor or management team. Work with minimal supervision; must be responsible and able to timely initiate appropriate work activities
  • Assist the head of Quality Department to ensure quality records meet FDA and ISO 9001-2000 requirements.
  • Help manage all aspects of the quality program
  • Assist in preparation for different audits, i.e. FDA, ISO, NSF/Organic, IASC, Kosher, GFCO, etc.

Qualifications

  • Minimum of High School Graduate
  • At least two years' experience in manufacturing of FDA regulated products.
  • Knowledge of cGMP in pharmaceutical or cosmetic products.
  • Knowledge of sampling and measurement quality tools.
  • Good oral and written communication skills; speak and write English.
  • Basic mathematics skills.
  • Knowledge of ISO 9001 preferred.
  • Knowledge of using measurement tools and equipment's.
  • Excellent communication skills and ability to work with internal/external clients.
  • Ability to work in a team environment, prioritize and multi task.
  • Excellent organizational skills and strong computer experience.
  • Ability to work with a minimum of supervision.
  • Must be detail oriented and willing to learn new procedures.
  • Able to work any shift, and overtime as required.
  • Good problem solving and experience with cosmetic industry manufacturing process
  • Basic knowledge of GMP procedures and record keeping
  • Ability to perform product hold investigation and reporting
  • Takes initiative to champion quality improvement ideas.
  • Ability to maintain an effective working relationship with all contacts both inside and outside the company.
  • Ability to accept new ideas and implement change in processes and procedures as needed.
  • Overtime required as needed.

Kathryn Bonilla 
Recruiter  
Volt Workforce Solutions
1515 West 190th Street #103 Gardena, CA 90248
t 562.384.5327 |  310.316.8523 | 23510
kbonilla@volt.com