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Job Location | Guelph, ON |
Education | Not Mentioned |
Salary | Not Disclosed |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Full Time |
The Johnson & Johnson Guelph site is a member of the Johnson & Johnson Family of Companies, the worlds most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. In Canada, Johnson & Johnson Inc. markets innovative consumer products focusing on skin and hair care, baby care, wound care, oral health and womens health as well as a broad range of well-known and trusted over-the-counter products.Johnson & Johnson Inc. employs approximately 400 people at its Guelph, Ontario manufacturing site.Role summary:To support aspects of Quality Systems related to products manufactured at the Johnson & Johnson Guelph Campus. To enable quality assurance activities that support product launch, product approval, post launch changes and document management processes. To assist in the management, development and implementation of processes/activities associated with the Tru specification and document system, EtQ Change Control, Standard Operator Procedures (SOPs), controlled document issuance and other document management processes. If you are looking for a role in which to gain an understanding of a Q&C program within a regulated GMP environment, this role is for you!Major responsibilities: