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Quality Assurance Intern jobs at Ge Healthcare in Canada

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23.08.2025
GEH

GE HealthCare Quality Assurance Intern Canada, Ontario

Limitless High-tech career opportunities - Expoint
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...
Description:
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.


Responsibilities:

  • 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.

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

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.

Show more
Limitless High-tech career opportunities - Expoint
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...
Description:
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.


Responsibilities:

  • 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.

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

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.

Show more
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