QC Inspector

Ultimate Staffing; Camarillo (CA); On-site; USD 32,000 - 33,000; Full time

Job summary

Ultimate Staffing in Camarillo is seeking a Quality Control Inspector to perform inspections across incoming materials, in-process items, and finished goods, ensuring compliance with quality standards and SOPs. The position offers a 5:00 AM to 1:30 PM schedule, Monday through Friday, on a direct hire basis, with a second shift available; pay ranges from $23 to $24 per hour.

Requires understanding of global pharmaceutical regulations (ISO 9001/13485 and 21 CFR Parts 210/211 or 820) and at least

Qualifications

• Understanding of global pharmaceutical product regulations (ISO 9001/13485, 21 CFR Parts 210-211/820).
• Experience performing GMP operations following SOPs, maintaining training and documentation.
• Minimum 2 years' experience with technical documentation for quality activities in pharma/medical device environments.
• Strong organizational, communication, and teamwork skills.

Responsibilities

• Perform quality control inspections at all production stages.
• Inspect incoming materials, in-process, and finished goods.
• Document observations and recommend process improvements.
• Initiate nonconformance reports and support quality investigations.
• Ensure compliance with quality standards and procedures.
• Coordinate with multiple facilities within a 2-mile radius.

Skills

GMP operations

Quality inspections

Document control

Nonconformance reports

Regulatory knowledge

Education

High School Diploma

Tools

Calipers

Tape measures

Rulers

Pin gauges

Job description

Quality Control Inspector Needed in Camarillo

Pay range: $23 - $24/hour

Monday - Friday

5am - 1:30pm

(2nd shift also available)

Direct Hire

Must Have

• Understanding of global pharmaceutical product regulations with experience with ISO 9001 manufacturing.
• 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.

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.

Key responsibilities include conducting incoming, in-process, and final inspections, documenting findings, initiating nonconformance reports, supporting quality investigations, and ensuring compliance with quality standards and procedures.

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.
• o Incoming inspections
• o In-process inspection.
• o Final Inspection release of finished goods.
• o Document review.
• o 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.