2018 MRL Regulatory Portfolio and Submission Management Intern Job

Employer
Merck
Location
Gwynedd, PA, US
Posted
October 12 2017
Organization Type
Pharma
Requisition ID: REG003147

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.



Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 


 


The Regulatory Portfolio and Submission Management (RPSM) Organization is responsible for the execution of regulatory strategy to get and keep products on the market through the authorization, planning, and management of timely, compliant, and high quality regulatory and safety submissions. 

  • The Intern position within RPSM would be involved with the supporting activities tied to submission delivery. 

  • Daily activities may involve but are not limited to coordination of data in regulatory systems, support of process improvement initiatives, and completion of supporting documentation.   

  • The Intern position will/may also work directly with the Regulatory Submission Manager (RSM) or Regulatory Report Coordinator (RRC) to assist with the creation and project management of routine periodic submission plans to ensure correct components and timelines are captured to support on-time, right first time release of regulatory and safety submissions. 
Qualifications



Education:

  • Required: Current student pursuing a BA/BS degree in a Life Sciences discipline, Biology, Biochemistry, Immunology, Microbiology, Molecular Biology, Physiology, or other Biology related degree program. 

  • Required Experience:


    • Must have excellent written and verbal communication and interpersonal skills 

    • Strong document management and organizational skills

    • Project management  

    • Initiative, leadership, and ownership of deliverables

    • Be a self-starter, fast learner and able to multi-task and work in fast-paced team environment

    Preferred Experience:

  • Proficient with computer systems (MS Office necessary; Advanced Excel and Word skills preferred) and document management systems (i.e. FirstDoc, Documentum, SharePoint)

  • Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 


     


    If you need an accommodation for the application process please email us at staffingaadar@merck.com.


      


    Search Firm Representatives Please Read Carefully: 


    Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.


     


    Visa sponsorship is not available for this position.


     


    For more information about personal rights under Equal Employment Opportunity, visit:


     


                EEOC Poster


                EEOC GINA Supplement 




    FTP2018



    Job: Regulatory Affairs Generic
    Other Locations:
    Employee Status: Temporary
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    Company Trade Name: Merck