4 jobs found in San Diego, CA

Work Flexibility: Onsite Schedule: 1st Shift, Monday to Friday start time between 8AM - 5:00PM Overtime based on business needs   What you will do - The Document Control Coordinator supports Operations, R&D, RA and QA activities by preparing, reviewing, routing, approving and archiving Quality System documents as well as the following below:   Review change orders and associated documentation to ensure compliance to company document and change control procedures. Supports the management of hardcopy and digital Quality System files Updates and maintains Document Control related logs Guides companywide on Quality System, Document Control function Tracks and facilitates timely documentation review and implementation. Verification of completion of DCO/ECO-related activities, such as material disposition and training to ensure closure of DCO/ECO following completion of these activities. Establish and maintain record retention timelines Assist...

Work Flexibility: Not available What You Get Out of the Internship     At Stryker, we believe that developing the next generation of talent is just as important as developing life-changing medical technologies. As an intern, you won’t just observe — you’ll contribute to meaningful projects, gain exposure to leaders who will mentor you, and experience a culture of innovation and teamwork that is shaping the future of healthcare. As an intern, you will:      Apply classroom knowledge and gain experience in a fast-paced and growing industry setting    Implement new ideas, be constantly challenged, and develop your skills    Network with key/high-level stakeholders and leaders of the business    Be a part of an innovative team and culture    Experience documenting complex processes and presenting them in a clear format        Who we want     Challengers. People who seek out...

Work Flexibility: Hybrid or Onsite Senior International Regulatory Affairs Specialist Irvine, CA Join a team focused on bringing medical technologies to market while ensuring compliance with global regulatory requirements. In this role, you will support regulatory strategy, submissions, and product lifecycle activities across a range of projects, partnering with cross-functional teams to navigate regulatory requirements and maintain product compliance in global markets. This position offers the opportunity to contribute to regulatory planning, agency interactions, and submission activities while collaborating with product development, quality, clinical, and manufacturing teams. 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 Assess regulatory intelligence and regulatory requirements to support local, regional, and global regulatory strategies. Evaluate...

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...