Quality Support Administrator Jobs

One of our clients is looking for a talented and highly motivated Quality Support Administrator. Please send your resume if you would like to pursue this opportunity and you authorize Infosoft to represent you for this position.

Here are the job position details for your review:

Job Title: Quality Support Administrator

Pay Rate: $20/Hr

Duration: 3 Months

Location: Issaquah, WA (Onsite)

Shift Timings : 1st Shift -(8:30 am to 5:00 pm)

This position is for the Healthcare Diagnostics division.

This position requires Contingent Workers to be fully vaccinated against COVID-19 unless they are granted a medical or religious exemption.

• The Quality Support Administrator is responsible for supporting QMS processes which may include, training, ship holds, risk management, CAPA, and other QMS-related activities.
• This role requires strong attention to detail, the ability to communicate, and a willingness to adapt to changing business needs.

Responsibilities may include some or all of the following:

• Other responsibilities as needed.
• Generates, reviews, and maintains QMS documents.
• Provides administrative support for external audits (regulatory or customer).
• Acts in a support capacity for critical QMS processes such as risk management, CAPA, document and change control, audits, training, and ship holds.
• Responsible for personal daily task management, training plans, and performance management.
• Reviews quality records for all related areas of responsibility.
• Assists with data preparation for Quality Management Reviews.

Pre-requisites

• Advanced knowledge of Microsoft Office applications, especially Word and Excel;
• Bachelor's degree in a scientific discipline or equivalent experience.
• 1+ years of Quality Management System (QMS) experience working in a regulated Good Manufacturing Process (GMP) environment

Personal competencies

• Ability to learn quickly and attention to detail.
• Capacity to easily adapt to changing priorities and timelines;
• Capacity to work both independently and in a team-oriented environment;
• Strong oral and written communication skills
• Ability to effectively complete the tasks entrusted;

Optional competencies

• Practical experience in a regulated industry
• Knowledge of regulatory requirements related to medical devices (Health Canada, FDA, TGA, etc.).
• Knowledge of international standards such as ISO 13485