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Job Details

Regulatory Affairs Specialist Operations

Company name
Valeant Pharmaceuticals International

Location
Bridgewater, NJ

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Profile

Overview
Valeant Pharmaceuticals International, Inc. is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization\u2019s potential and what we hope it will become.
 
The Regulatory Affairs Operations Specialist is responsible for updating global regulatory information in Global RIM system, and generating relevant reports from the system. The person will also assist the electronic/paper compilation and submittal of Regulatory submissions to Health Authorities.
 
Update regulatory data in Global RIM system, and assist publishing regulatory submission documents for global submissions
Responsibilities

Update regulatory data in RIM systems and generate reports from the system.
Archive documents according to archiving and document retention strategies
Promote and support RA system usage
Work with RA Ops managers to ensure readiness of submission documents in accordance with agency guidance
Perform QA/QC for submission documents and deliverables for submission-readiness
Promote document authoring standards
Other job responsibilities as needed
Key Relationships: Internal business functions related to managing global regulatory information, and publishing global regulatory submission documents

Qualifications

Working knowledge and understanding of regulatory requirements and regulations
Understanding of the drug development process
Working knowledge of electronic submission requirements to Health Authorities
Knowledge of good documentation practices and requirements for managing regulated records
Capable of utilizing IT systems supporting regulatory affairs such as document management, electronic publishing, and submission systems (e.g., SharePoint, Documentum, InSight Manager)
Skilled in basic technologies (e.g., MS Office Applications, Adobe Acrobat, MS Project)
Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies
2 years combined pharmaceutical experience and regulatory experience preferred
Bachelor\u2019s degree preferred

Be Aware of Recruiting Fraud
Valeant is an EEO/AA employer M/F/D/V.
 
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
 
To learn more please read Valeant\u2019s Job Offer Fraud Statement.

Company info

Valeant Pharmaceuticals International
Website : http://www.valeant.com

Company Profile
Valeant Pharmaceuticals International, Inc. (NYSE/TSX: VRX) is a multinational specialty pharmaceutical and medical device company that develops, manufactures and markets a broad range of prescription and non-prescription pharmaceutical products that make a meaningful difference in patients’ lives throughout more than 100 countries. Valeant’s primary focus is in the areas of dermatology and eye health.

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