Valeant Pharmaceuticals

Project Manager, Quality

Location US-NJ-Bridgewater | US-NY-Rochester | US-FL-Clearwater | US-SC-Greenville
Job ID
9753
Category
Quality
Pos. Type
Full Time

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’s potential and what we hope it will become.

 

Project management lead for strategic projects within the Global QA organization. Drive consistent practices that efficiently & effectively achieve desired results.

 

This role does not have any direct reports. 

Responsibilities


This position will be responsible for several projects; number of project will vary and depend on resource demand. Projects are high impact (compliance risk or efficiency improvement) and high complexity (global or large teams). Position will touch all product categories (drug, device, consumer). The person in this role will be expected to teach and institute consistent PMO practices, and drive critical thinking to achieve effective results through tools like Six Sigma and Business Process Modeling.

  • Project Manager for select strategic projects
  • Increase QA efficiency & effectiveness by providing planned and on-the-job PMO methodology training to Team Members and leveraged Project Managers
  • Maintain PMO software and Sharepoint to effectively communicate with Team Members and Management
  • Leverage knowledge and tools such as Six Sigma and Business Process Modeling to improve Team efficiency and results
  • Develop and maintain monthly metrics and progress reports
  • Set-up & lead Team Meetings, issue minutes, communicate risk, escalate issues as needed to deliver projects on-time, compliant, and efficient results

Internal Customers/ Business Partners:

Global QA, Internal and External Manufacturing, Supply Chain

Regulatory Affairs, Medical Affairs, Clinical, R&D

Commercial

Qualifications

  • Minimum Bachelor’s Degree in scientific or engineering discipline. Project Management experience or equivalent proven capability. Skills set in some of the following areas: Six Sigma, Business Process Modeling, Quality Control, Quality Assurance, and Compliance. Track record of problem solver and team leadership. Experience working in a changing environment and fast-paced organization as a member of cross-functional and multi-national teams. Capability in MicroSoft Project, Excel, Visio, and PowerPoint. Experience with MicroSoft Project On-Line is a plus.
  • Minimum of 8 years in Medical Device and/or Pharmaceutical Industry, experience as a Project Manager or tangible Project Management experience with strong skills in some of the following areas QA/QC, Compliance, related Consulting.

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’s Job Offer Fraud Statement.

 

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