QA/QC Specialist

QA/QC Specialist $28 - $32 per hour | Valencia, CA | On‑site | Permanent Medical Device Company – QA/QC Specialist A global provider of isotope-based technology, developing and manufacturing products used in medical, scientific, and industrial applications. Why join us? Competitive Base Room for advancement Full Benefits 401K and more… Job Details Key Responsibilities Work under the direction of the Quality Systems, Regulatory, or Radioassay leadership to support and maintain compliance with established quality programs. Provide regular updates on QA and QC activities through reports and team discussions. Support the upkeep of a compliant Quality Management System aligned with ISO9001, ISO13485, MDSAP, FDA21CFR820, NRC, BIS, DOT, ISO17025, CEMark, and other applicable regulatory standards. Assist with ongoing regulatory compliance requirements and updates as needed. Perform final quality checks across product lines and review outgoing orders, with exceptions as directed by leadership. Manage nonconformance reports (NCRs), including issuance, tracking, resolution, and documentation. Maintain accurate filing and organization of all quality records and documentation. Monitor production activities to ensure adherence to established procedures. Identify opportunities for process improvements and recommend updates where appropriate. Conduct incoming inspections of materials and components. Verify accuracy and readability of engravings completed internally or by external vendors. Support dimensional inspections of manufactured components. Review domestic and international orders for regulatory and license compliance. Assist in managing document control systems and processes. Update and revise quality documentation, including procedures, forms, drawings, and records. Maintain documentation systems and tools such as BPM platforms, eQMS, or document management software. Support approval of design documentation and engineering change orders. Contribute to the maintenance of technical files for regulated products. Participate in internal and supplier audits under the supervision of a lead auditor. Provide training to staff on quality procedures and inspection methods as needed. Travel periodically between local facilities and to supplier sites for audits or training. Perform additional responsibilities as assigned. Qualifications High school diploma required; associate or bachelor’s degree preferred. At least 3 years of experience in quality control or quality assurance. Prior exposure to documentation control, record keeping, or inventory tracking is preferred. Skills and Experience Strong written and verbal communication skills. High level of attention to detail and accuracy. Experience using inspection tools such as calipers, micrometers, and optical measurement equipment. Ability to perform final inspections and receiving inspections independently. Comfortable working both independently and collaboratively. Strong organizational skills with the ability to manage shifting priorities. Proficient in Microsoft Excel, Word, and Access. Ability to lift up to 50 pounds. Willingness to travel between local sites as needed. Equal Opportunity Statement Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. #J-18808-Ljbffr