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Qa Intern Jobs
Company | GE HealthCare |
Address | Mississauga, Ontario, Canada |
Employment type | TEMPORARY |
Salary | |
Category | Medical Equipment Manufacturing,Hospitals and Health Care,Pharmaceutical Manufacturing |
Expires | 2023-07-30 |
Posted at | 10 months ago |
Summary
Description:
The QA Intern is responsible for maintenance of Quality System metrics, reporting and operating mechanisms to help drive the site quality objectives.
Key responsibilities include:
Relocation Assistance Provided: No
Description:
The QA Intern is responsible for maintenance of Quality System metrics, reporting and operating mechanisms to help drive the site quality objectives.
Key responsibilities include:
- Participate in investigations of quality-related incidents, deviations, and non-conformities, and collaborate with cross-functional teams to implement corrective and preventive actions (CAPAs).
- Assist in executing quality control procedures and protocols to ensure compliance with regulatory requirements, industry standards, and internal quality guidelines.
- 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.
- Collect, organize, and analyze data from investigations to identify trends, patterns, and areas for improvement.
- Collaborate effectively with colleagues and cross-functional teams to ensure open communication, knowledge sharing, and alignment of quality objectives.
- Identify and ensure timely closure of quality investigations for the site.
- 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.
- Participate in annual GMP Record reviews.
- Assist in product batch release activities.
- Complete all planned Quality & Compliance training within the defined deadlines.
- Identify and report any quality or compliance concerns and take immediate corrective action as required.
- Ability to work independently as well as in a team environment.
- Strong analytical and problem-solving abilities.
- Strong computer skills including proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Strong attention to detail and ability to meticulously follow instructions and procedures.
- Currently pursuing a college certification or degree in Quality Assurance, pharmaceutical sciences, chemistry, biology, or a related field (or recently graduated).
- Excellent organizational and documentation skills.
- Knowledge of quality assurance principles, regulatory requirements, and industry guidelines (e.g., cGMP)
- Effective communication skills, both verbal and written.
Relocation Assistance Provided: No
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