4 jobs found in Torrance, CA

Work Flexibility: Remote Staff Clinical Safety Specialist - Remote As a Staff Clinical Safety Specialist, you will serve as a clinical safety subject matter expert across multiple studies, leading safety event review, adjudication, reporting, and process oversight while partnering with cross-functional teams to support consistent and compliant clinical study execution. This role combines clinical safety expertise, regulatory knowledge, and operational leadership to ensure accurate assessment, documentation, coding, and reporting of clinical safety events across a global study portfolio. Work Flexibility: Remote What You Will Do Lead clinical safety oversight activities across assigned studies, including identification, assessment, adjudication, and reporting of adverse events and other safety-related events. Review and evaluate adverse events, serious adverse events, protocol-defined endpoints, and other safety signals to ensure accurate and timely...

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...

Work Flexibility: Onsite Stryker is hiring an Associate Manager, Quality Assurance in Irvine, CA to lead a high-performing Quality Operations team and drive quality excellence across manufacturing and business functions. In this role, you will provide leadership and direction for quality assurance activities with a strong focus on compliance, risk prevention, continuous improvement, and operational effectiveness. You will be responsible for ensuring adherence to Stryker Corporate and SGS requirements, Quality System Regulations, and applicable industry standards while fostering a culture of engagement, accountability, and quality ownership. This position plays a key role in delivering both compliance and business objectives, supporting product quality, process improvements, and overall organizational success. What you will do: Lead and develop a Quality Engineering team, providing guidance and support to manufacturing and cross-functional partners while promoting a...