– Contribute to the maintenance and continuous improvement of the Record Management systems and processes
– Perform the creation and revision of site and/or corporate level quality documents that support operations to ensure compliance with company guidelines and quality standards
– Perform activities associated with the receipt, retrieval, maintenance and tracking of records utilizing the record management system
– Perform routine administrative activities such as filling, scanning, and archiving
– Create and edit controlled documents consistent with current formats
– Support the QA Manager in analyzing quality data
– Liaise with external Vendor on the maintenance of compactors and off-site storage of records
– Support regulatory inspections by providing document administrative and record retrieval tasks
Job Requirements:
– Must have a Bachelor’s degree
– Technically savvy on MS Office applications
– Experience in the medical device or related industry is an asset
– Knowledgeable in the healthcare/pharmaceutical quality regulations and compliance
– Knowledgeable in audits and inspections
– Effective time management skills
– Ability to work in a team environment and independently
If you think you are the right candidate for the role, please email your updated resume in Word to [email protected] AND EARN A $50 GIFT CARD! For more details, click here.
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