2018 MRL Resource Management Intern Job

Employer
Merck
Location
Gwynedd, PA, US
Posted
October 12 2017
Discipline
Other
Organization Type
Pharma
Requisition ID: ADM008688

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. 


 


Merck Research Lab is currently seeking an intern to assess the productivity of external partners within the Global Regulatory Affairs and Clinical Safety organization.   


The intern will work to identify findings to make recommendations to help optimize the organization’s operating model. By working across multiple functional areas, regions, and key stakeholders, the intern will:




  • Validate planning models  

  • Develop productivity metrics for a variety of activities performed externally
Qualifications


Education:

  • Required: Current student pursuing a BA/BS degree with a focus towards business operations and analytics.

  • Candidates must be returning to school in the Fall of 2018.

  •  Required Experience:

  • Candidates must have a business operations mindset

  • Candidates must have experience working with and analyzing qualitative and quantitative data sets

  • Candidates must be motivated, independent, and an out-of-the-box thinker

  • Candidates must be available to work full-time for 10-12 weeks beginning in May or June of 2018.

  • Preferred Experience:



  • Experience in productivity or process improvements (Six-Sigma, etc.)

  • Experience incorporating ambiguous data into analyses

  • Experience in business planning, metrics development, and/or business analytics role

  • Specific interest in pharmaceuticals and/or regulatory and safety is preferred.  


  • 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: Administrative Svcs Generic
    Other Locations:
    Employee Status: Temporary
    Travel: Yes, 5 % of the Time
    Number of Openings:
    Shift (if applicable):
    Hazardous Materials:
    Company Trade Name: Merck

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