Overview
QC Inspector Jobs in Camarillo, California, USA at Ultimate Staffing
Quality Control Inspector Needed in Camarillo
Direct Hire and / or Temp to Hire Available
Base Pay Range: $21.00/hr – $24.00/hr
Schedule: Monday – Friday, 6:30am – 4:00pm (OT and Saturdays may also be available)
Must Have
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, including 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 tests during the manufacture of products. Inspects incoming materials and products at different stages of production. Records observations and makes recommendations for improving processes.
Essential Functions
Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements.
Initiate nonconformance reports (NCR).
Perform all aspects of testing related to manufacturing:
Incoming inspections
In-process inspection
Final Inspection release of finished goods
Document review
Support cross-functional departments in investigating potential non-conformance observed.
Ensure 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.
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, including 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, and 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 personal attributes: integrity, 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, and 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.
Seniority Level
Mid-Senior level
Employment Type
Full-time
Job Function
Manufacturing and Quality Assurance
Industries
Manufacturing
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Title: QC Inspector
Company: Ultimate Staffing
Location: Camarillo, California, USA
Category: Quality Assurance – QA/QC, Manufacturing / Production
