Job Details

Note: This is a Quality Systems role focused on medical device manufacturing (onsite in Irvine, CA); candidates from IT/Software QA/Automation backgrounds will not be considered.

Job Description:

As a Quality Systems Analyst, you'll be at the forefront of transforming Client's procedures to establish Critical Care Quality Management System.

Key Responsibilities:

• You will be collaborating with cross functional stakeholders to understand business needs and develop requirements, processes and workflows.
• You will be supporting setting up and training of new Supplier Management Quality Systems for the new organization.
• You will partner effectively with all levels of the organization to drive results, proactively identify and resolve problems and escalate as required.
• Post spin off, you will support SQE team to ensure compliance to quality system specific and requirements. In addition you will continue to drive improvement of current practices and work with the appropriate functions to implement changes or participate in their implementation.

Additional Skills:

• Experience in a quality and/or manufacturing environment in the medical device industry required.
• Proven expertise in MS Office Suite.
• Good project management skills and related software tools preferred.
• Excellent written and verbal communication skills including negotiating and relationship management skills.
• Strong problem-solving and critical thinking skills.

Education and Experience:

• Bachelor's Degree or equivalent in in related field of study.
• Experience in a quality and/or manufacturing environment in the medical device industry required.
• 2-4 years of experience required.