JOB DESCRIPTION SUMMARY

As the Quality Assurance Intern, you will be responsible for supporting our Quality Assurance team by assisting in maintaining GMP compliance, participating in investigations of quality-related incidents, and contributing to process improvements to ensure adherence to regulatory standards and site quality objectives.
GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

REQUIRED QUALIFICATIONS:

• Currently pursuing (or recent graduate of) a college certification or degree in Quality Assurance, pharmaceutical sciences, chemistry, biology, or a related field
• Must be willing to go in office in Mississauga, ON
• Knowledge of quality assurance principles, regulatory requirements, and industry guidelines (e.g., cGMP)
• Strong attention to detail and ability to meticulously follow instructions and procedures.
• Excellent organizational and documentation skills.
• Strong computer skills including proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
• Strong analytical and problem-solving abilities.
• Effective communication skills, both verbal and written.
• Ability to work independently as well as in a team environment.

DESIRED QUALIFICATIONS:

• Graduate of (or current student of) a Quality Assurance and Regulatory Affairs program
  We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership –always with unyielding integrity.
  Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
  

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LI-Hybrid

• Assist in executing quality control procedures and protocols to ensure compliance with regulatory requirements, industry standards, and internal quality guidelines.
• Participate in investigations of quality-related incidents, deviations, and non-conformities, and collaborate with cross-functional teams to implement corrective and preventive actions (CAPAs).
• Collect, organize, and analyze data from investigations to identify trends, patterns, and areas for improvement.
• Support compliance activities by reviewing and ensuring adherence to applicable regulations, guidelines, and quality standards (e.g. cGMP).
• Contribute to process improvement initiatives by suggesting and implementing efficiency enhancements, quality control optimization, and best practices.
• Collaborate effectively with colleagues and cross-functional teams to ensure open communication, knowledge sharing, and alignment of quality objectives.
• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
• Complete all planned Quality & Compliance training within the defined deadlines.
• Assist in product batch release activities.
• Participate in annual GMP Record reviews.
• Identify and report any quality or compliance concerns and take immediate corrective action as required.
• Identify and ensure timely closure of quality investigations for the site.