QC Inspector

Ultimate Staffing Services; Camarillo (CA); On-site; USD 33,000 - 36,000; Full time

Benefits offered by this job

Excellent benefits package

Job summary

Ultimate Staffing Services is seeking a QC Inspector in Camarillo, CA to perform quality control inspections across manufacturing stages, including incoming, in-process, and final checks. This role requires hands-on experience with measuring tools and adherence to GMP standards.

The position offers direct hire, with a schedule Monday–Friday, 5am–1:30pm, and potential overtime including weekends. Strong documentation and teamwork are essential.

Qualifications

• 2+ years of quality control inspection experience.
• Experience using handheld measuring tools including calipers, micrometers, and measuring tapes.
• Cleanroom experience or ISO 7 exposure preferred.
• Incoming materials, in-process, and final inspection experience.
• Experience with non-conformance reporting including NCR/MRR processes.

Responsibilities

• Perform quality inspections across all manufacturing stages and ensure compliance with regulatory requirements.
• Conduct inspections and testing related to manufacturing processes.
• Initiate nonconformance reports (NCR) for identified non-conformances.
• Manage incoming, in-process, and final inspections and release of finished goods.
• Review documents and support cross-functional teams in investigations of potential non-conformances.

Skills

Quality control

Inspection

Documentation

SOP compliance

Math skills

Education

High School Diploma or equivalent

Tools

Calipers

Micrometers

Measuring tapes

Job description

QC Inspector (JN -052025-397726) Camarillo, California

Salary: USD24 - USD24 per hour + Excellent Benefits Package

Quality Control Inspector Needed in Camarillo -Multiple Openings

Direct Hire

Pay range: $$26/hour

Monday - Friday

5am - 1:30pm

Other Start Times Available

Must Have

• 2+ years of Quality ControlInspectorexperience
• Experience using handheld measuring tools, including calipers, micrometers, and measuring tapes
• Cleanroom experience or exposure, preferably ISO 7
• Incoming raw material, 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

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:
• 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