QC Inspector

Base pay range: $23.00/hr - $24.00/hr

Schedule:

• Monday - Friday
• 7am - 3:30pm

Must Have:

• Understanding of global pharmaceutical product regulations, ISO 9001 and/or 13485:2003, 21 CFR Parts 210 and 211 and/or Part 820.
• Demonstrated ability to perform GMP operations following SOPs, maintaining training and good documentation practices.
• Minimum 2 years’ experience with technical documentation for quality activities, including quality inspections and corrective actions in pharmaceutical or medical device environment.

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

• Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements.
• Conduct inspection and testing related to:
  • Incoming inspections
  • In‑process inspection
  • Final inspection release of finished goods
  • Document review
• Initiate nonconformance reports (NCR).
• Perform all aspects of testing related to manufacturing.
• Support cross‑functional departments in investigating potential non‑conformance observed.
• Ensure 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.

• High school diploma or equivalent with 2 years of experience in quality control inspections.

• Understanding of global pharmaceutical product regulations, ISO 9001 and/or 13485:2003, 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 2 years’ experience with technical documentation for quality activities, including quality inspections and corrective actions in pharmaceutical or medical device environment.
• Solid organizational and planning skills.
• Effective communication skills, both verbal and written, with good interpersonal skills interdepartmentally and with external vendors and contractors.
• Ability to work effectively and efficiently in a team environment.
• Personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
• Personal accountability for results and integrity.
• Eagerness to learn and continuously improve.
• Uncompromising dedication to quality.
• Good general mathematical skills.
• Knowledge and use of measuring devices such as calipers, tape measures, rulers, pin gauges.

• Mid‑Senior level

• Full‑time

• Manufacturing, Production, and Quality Assurance

• Food and Beverage Manufacturing
• Manufacturing
• Pharmaceutical Manufacturing

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, and Los Angeles County Fair Chance Ordinance.