6 jobs found in Ventura, CA

Work Flexibility: Onsite Summary: This role provides hands-on technical support for manufacturing process development, equipment installation and validation, and documentation required to successfully launch and sustain production processes. The position partners closely with Engineering and Operations to troubleshoot issues, support continuous improvement initiatives, and ensure compliance with quality, GMP, GDP, and safety requirements. A key focus of this role is supporting production readiness through process stabilization and training during new process implementations. What you will do: Develops and recommends procedures and methods and prepares technical reports and documentation. Performs technical evaluations of events to determine root cause and recommends corrective action. Actively interface with cross-functional team members always practicing good teamwork in support of day to day operating requirements. Monitoring and management of manufacturing...

Work Flexibility: Onsite Schedule: Monday- Friday 3:30pm-11:30 pm with overtime as needed by the business. What You'll do: Provide technical support to engineers and scientists on a variety of projects and initiatives. Set up, operate, and maintain equipment used in testing, manufacturing, or technical processes. Troubleshoot equipment, process, and production issues to identify and resolve problems efficiently. Perform routine technical tasks following established procedures, work instructions, and quality standards. Assist with technical evaluations and root cause investigations to support corrective actions and continuous improvement efforts. Collect, organize, and analyze technical data, maintaining accurate reports and documentation. Collaborate with cross-functional teams to support projects, meet deadlines, and achieve operational goals. Maintain compliance with safety, quality, and operational requirements while supporting daily activities....

Work Flexibility: Hybrid or Onsite Location: 510 Technology Drive STE #300, Irvine, CA Schedule : Monday – Friday, 8am – 5pm Overtime based on business needs What you will do The Customer Service Representative serves as the primary point of contact for customers before and after sales, supporting the sales team by fostering strong client relationships that directly impact service and product revenue. This role involves handling customer inquiries, coordinating with internal departments to resolve issues related to product information, pricing, shipping, warranty claims, and repairs, while also identifying new and add-on business opportunities. Serve as a liaison for internal and external customers, answering calls and processing email requests with professionalism and accuracy Place and process product orders while partnering with the Warehouse and Logistics team to ensure timely distribution Build and maintain strong relationships with customers and...

Work Flexibility: Onsite Schedule: Monday - Friday, 6:00am- 2:30pm, OT as needed by the business What You'll Do Serve as the quality subject matter expert for product and process quality standards. Ensure compliance with cGMPs and regulatory requirements (FDA, BSI, TUV, and other medical device agencies). Act as the first point of contact for daily production line quality issues. Investigate product and process concerns, identify root causes, and support corrective actions. Partner with Quality Engineers and cross-functional teams to reduce risk and improve processes. Deliver defect awareness and quality training to production associates. Support the management and disposition of non-conforming materials and products. Segregate and contain product when quality discrepancies are identified. Conduct audit readiness checks and support internal quality audits. Monitor, trend, and analyze key quality metrics and performance data. Review customer...

Work Flexibility: Hybrid or Onsite Staff International Regulatory Affairs Specialist Irvine, CA In this International Regulatory Affairs role, you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways. This is a meaningful opportunity to drive operational excellence, collaborate across global teams, and directly influence our ability to deliver safe, effective products to patients internationally. Work Flexibility: Hybrid: candidates must reside within commuting distance of Irvine, CA and be able to work onsite several days per week. What You Will Do Evaluate products, product changes, and manufacturing changes to determine regulatory classification, jurisdiction, submission requirements, and approval pathways. Assess regulatory intelligence and evaluate evolving regulations to support local, regional, and global regulatory strategies. Advise cross-functional teams on regulatory requirements throughout...

Work Flexibility: Onsite Schedule: Monday - Friday, 3:30pm- 12:00am, OT as needed by the business What You'll Do Serve as the quality subject matter expert for product and process quality standards. Ensure compliance with cGMPs and regulatory requirements (FDA, BSI, TUV, and other medical device agencies). Act as the first point of contact for daily production line quality issues. Investigate product and process concerns, identify root causes, and support corrective actions. Partner with Quality Engineers and cross-functional teams to reduce risk and improve processes. Deliver defect awareness and quality training to production associates. Support the management and disposition of non-conforming materials and products. Segregate and contain product when quality discrepancies are identified. Conduct audit readiness checks and support internal quality audits. Monitor, trend, and analyze key quality metrics and performance data. Review...