Quality Systems and Compliance Fall 2024 Co-Op
at Johnson Johnson
Guelph, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Aug, 2024 | Not Specified | 12 May, 2024 | N/A | Outlook,Computer Skills,Communication Skills,Collaboration,Microbiology,Chemistry,Excel,Organization Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
WHO WE ARE
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made up with 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.
Responsibilities:
This position’s primary responsibility is to assist with implementation of quality systems based on business, regulatory, and customer requirements. This role has responsibility to assist with Change Management, Specification/Document Management, Systems Support (P360), and Marketed Product Stability Support. These Quality Systems activities support product launch, product release processes, life cycle management, and post market surveillance. This role ensures that Kenvue Canada operates in compliance with internal procedures, Canadian regulatory requirements, and Kenvue Quality Standards.
Key Responsibilities:
- Administrator for EtQ Symphony system, a repository for change control, corrective action, and investigation documents.
- Author and revise documents then lead routing of document for approvals through the TRU system.
- Liaison with multiple business partners through troubleshooting EtQ Symphony problems and ensure timely action to meet metrics.
- Create change control meeting agendas, notifications, and action list generation and complete metrics.
- File documentation, distribute and organize samples. (as required)
- Lead and provide support to continuous improvement initiatives within the Quality Compliance department through effective review and analysis of information.
- Support monthly Kenvue Franchise/Commercial Quality metrics meetings. Collect, compile, and present monthly metrics to Leadership and appropriate stakeholders/SMEs. (as required)
- Complete administration activities for Marketed Product Stability program
- Source, review, and route Marketed Product Stability results in alignment with Kenvue local procedures and Canadian regulations
- Support Annual Product Quality Review program in alignment with Kenvue local procedures and Canadian regulations (as required)
Working Conditions
- Appropriate safety measures must be monitored and followed (Internal & External)
- Ergonomic considerations (workstation design, sitting, reaching, standing)
- Flexible work model (i.e remote) can be considered
- Periodic travel may be required
Qualifications
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
A science-based discipline such as chemistry microbiology or engineering
Proficient
1
Guelph, ON, Canada