QC Inspector

Ultimate Staffing; Camarillo (CA); Presencial; USD 30.000 - 42.000; Jornada completa

Descripción de la vacante

Ultimate Staffing in Camarillo, CA is seeking a Quality Control Inspector for first or second shift to support manufacturing operations. The role requires hands-on inspections of incoming materials, in-process items, and finished goods with a strong focus on accuracy and regulatory compliance.

You will interpret blueprints and engineering drawings, use calipers and micrometers, maintain NCR/MRR records, and ensure documentation is complete in a cleanroom environment (ISO 7+).

Formación

• 2+ years of quality control inspection experience.
• Proficiency interpreting blueprints and engineering drawings.
• Experience with handheld measurement tools (calipers, micrometers, tapes).
• Cleanroom experience or ISO 7+ exposure.
• Familiarity with NCR/MRR non-conformance reporting.

Responsabilidades

• Perform quality inspections and tests across production processes.
• Inspect incoming materials, in-process items, and final products.
• Record observations and recommend process improvements.
• Initiate NCRs for non-conforming material.
• Ensure inspections are documented and traceable.
• Support safety requirements and housekeeping.

Conocimientos

QC inspections

Blueprint interpretation

Regulatory compliance

Attention to detail

Team collaboration

Educación

High School Diploma or equivalent

Herramientas

Calipers

Micrometers

Tape measures

Descripción del empleo

Quality Control Inspector Needed in Camarillo

Direct Hire

Pay range: $26/hour

1st Shift Available

Monday - Friday

5am - 1:30pm

2nd Shift Available (+$1.00/hour for shift differential)

Monday - Friday

3pm - 11:30pm

Must Have

• 2+ years of Quality Control Inspector experience
• Experience interpreting BluePrints / Engineering Drawings (very important and you must be highly proficient as they work with BluePrints all day)
• Experience using handheld measuring tools, including calipers, micrometers, and measuring tapes
• Cleanroom experience or exposure needed, preferably ISO 7 (or higher)
• Incoming raw material, in-coming, in-process, and final inspection experience
• Experience with non-conformance reporting, including NCR/MRR processes
• Flexibility to work overtime as business needs require, including weekends
• Ability to work in the cleanroom 85% - 90% of the time
• Prefered expereice with particualate matter inspections

Job Summary

Performs quality control inspections in all aspects of operations, checks, and test during the manufacture of products. Inspect incoming materials, and products at different stages of production. Records observations and make recommendations for improving processes.

Essential Functions

• Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements;
• Conduct inspection and testing related to:
  • Incoming product.
  • First article.
  • In-process.
  • Final.
• Initiate nonconformance reports (NCR).
• Performs all aspects of testing related to manufacturing.
  • Incoming inspections
  • In-process inspection.
  • Final Inspection release of finished goods.
  • Document review.
  • Supports cross functional departments investigate potential non-conformance's observed
• Ensures that all inspections and procedures are properly completed and documented.
• Perform pre and post-inspection of product gamma irradiation process.
• Approve or reject raw materials with respect to quality standards and communicate results to all pertinent parties.
• Initiate nonconformance reports (NCR) for all non-conforming material identified throughout operations
• Prepare and submit Metrics reports to the quality supervisor or QC lead
• Comply with all safety requirements ensuring work areas meet standards.
• May be required to report to multiple facilities within a 2-mile radius.
• Job Order document review and release
• Other duties as assigned

Education

• High School Diploma or equivalent with 2 years of experience in quality control inspections.

Required Experience & Competencies

• Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820.
• Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices.
• Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment.
• Solid organizational and planning skills required.
• Ability to communicate effectively, verbally and in writing, demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors.
• Must be able to work effectively and efficiently in a team environment.
• Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
• Must display personal accountability for results and integrity.
• Must display eagerness to learn and continuously improve.
• Must have uncompromising dedication to quality.
• Good general mathematical skills.
• General knowledge and use of measuring devices such as calipers, tape measures, rulers, pin gauges

All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, Los Angeles County Fair Chance Ordinance, and San Francisco Fair Chance Ordinance.