Job Description

Reference # : 18-02967Title : Contract Project Manager (Regulatory & Compliance - TSE)
Location : Pennington, NJ
Position Type : Contract
Experience Level : Start Date / End Date : 03/19/2018 / 09/18/2018
Assignment Detail
Industry:Biotech/PharmaJob Category:Scientific / Clinical
Description
Contract Project Manager
(Regulatory & Compliance – TSE)

Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Contract Project Manager (Regulatory & Compliance - TSE) for our client in Pennington, NJ.

Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you are up to the challenge, then take a chance at this rewarding opportunity!

Job Responsibilities:
  • The candidate will be responsible for assisting in processes related to the clients TSE (Transmissible Spongiform Encephalopathies) program.
  • Develop an in-depth knowledge of global TSE requirements and be able to apply these requirements to the job.
  • Maintain TSE information repositories within BMS.
  • Effectively network with key business partners to achieve assigned objectives.
  • Evaluate documentation for compliance to current requirements and help with securing documentation for the preparation of clients TSE Regulatory Compliance product statements.
Job Requirements/Education:
  • Excellent oral and written communication skills.
  • Proficient navigation of electronic systems, (e.g., MS Excel, and Adobe Acrobat) including formatting and electronic management of data and information.
  • The candidate will have demonstrated ability to be a strong team member with the ability to drive projects to completion on time.
  • Knowledge of global BSE/TSE regulations and guidances a plus.
  • Knowledge of product formulation and manufacturing processes desirable.
  • Ability to handle multiple projects and prioritize work independently.
  • Basic understanding of the drug development process plus an integrated view of the technical, manufacturing and commercial aspects of the pharmaceutical business.
  • Minimum of 2-5 years of experience in the pharmaceutical industry with a BS degree in a scientific discipline, chemistry or pharmacy preferred.
  • Experience in GMP auditing and/or CMC regulatory a plus.

    Interested in applying?
    Contact Joy Retanan at (646) 695-2949 or at http://www.linkedin.com/pub/joy-retanan/85/4ba/333 or send your resume to Joy.Retanan@eclaro.com now.


    Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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