QC Inspector

Ultimate Staffing; Camarillo (CA); On-site; USD 33,000 - 39,000; Full time

Job summary

Ultimate Staffing is hiring a Quality Control Inspector in Camarillo to perform inspections across all manufacturing stages, ensuring compliance with regulatory and internal standards. The role involves reviewing raw materials, in-process items, and finished goods, with emphasis on NCR/MRR processes and meticulous documentation.

The ideal candidate has at least 2 years in quality control, hands-on experience with calipers, micrometers, and tapes, and the flexibility to work overtime, including

Qualifications

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

Responsibilities

• Perform quality inspections across operations, checks and tests during manufacturing.
• Inspect incoming materials and products at different production stages.
• Record observations and recommend process improvements.
• Ensure inspections and procedures are completed and documented.
• Initiate NCRs for non-conforming materials.
• Prepare and submit metrics reports to QC lead or supervisor.
• Support safety requirements and maintain clean work areas.
• May report to multiple facilities within a 2-mile radius.

Skills

Quality control

Measurement tools

Cleanroom exposure

Inspection skills

NCR/MRR processes

Overtime availability

Education

High School Diploma or equivalent

Tools

Calipers

Micrometers

Measuring tapes

Job description

Quality Control Inspector Needed in Camarillo

Direct Hire

Pay range: $$26/hour

Monday - Friday

5am - 1:30pm

Other Start Times Available

Must Have

• 2+ years of Quality Control Inspector experience
• 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

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.