Remotely
regulatory affairsregulatory submissionslabelingms officeall otheredmsrimglsdocx tool
Job Description
📋 Description
- Assist with creation and maintenance of labeling in RIM/global systems for products (Rx, OTC
- Support lifecycle management of product submissions and authorizations in RIMGLS.
- Manage US SPL and CA XML-PM listings and products in development.
- Represent Regulatory Labeling-Operations in cross-functional meetings.
- Provide guidance to internal customers on regulatory labeling issues.
- Educate teams on regulatory information topics and ensure timely labeling responses.
🎯 Requirements
- Bachelor’s in pharmacy, biology, chemistry, or related sciences; or Associate’s with 8+ years
- 3+ years in regulatory affairs, R&D, or related area.
- Experience in global matrix environments with strong communication and attention to detail.
- Experience with electronic submissions, software tools, and data standards; regulatory strategy
🎁 Benefits
- Comprehensive benefits package
- Opportunity for career development
- Inclusive, diverse workplace
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