• Clinical Supplies Associate - Logistics

    Job Locations - | US-PA
    Posted Date 2 weeks ago(8/6/2018 10:21 AM)
  • Overview

    Do you want to be responsible for packaging and labeling duties per standard operating procedures within Clinical Supplies



    Who are we?

    We Are PRA.


    We are 15,000+ employees strong, operating in more than 85 countries. We are committed to saving lives, and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We are getting live saving drugs into the hands those who need them most.


    Who Are You?


    You are an experience professional with a passion for clinical supplies. You are organized, but flexible and adaptable to unexpected changes. You can easily envision the bigger picture, without losing sight of the day-to-day tasks. You can provide excellent leadership to not only your project teams, but also to clients. You are excited and enthusiastic. You motivate your teams to do great work and collaborate easily with your clients. Most of all, you want to do it in a place where you’re more than an employee number. A place you love working.


    Still here? Good. Because if this is you, we’d really like to meet you.


    1. Receipt of shipments
      • Bulk Goods Locations (Carousel, Cold Vaults, Warehouse, Freezers)
      • Receipt Process
      • Receiving Documentation
      • POMS Transactions
      • SAP Transactions
      • Scale Check Procedure
    2. Processing CPOs
      •  Staging Material for Packaging CPOs
      •  Processing Movement of Material for CPOs in POMS
    3. Clinical Drug Returns, Relabeling, Discards
      • Processing of Clinical Drug Returns
      • Relabeling of Bulk Material and Finished Goods
      • Processing Clinical Drug Discards, R431 Procedure
    4. Cycle Counts and Freezer/Cold Vault Maintenance
      • Bulk Cycle Counts
      • Freezer and Cold Vault Chart Inspection and Changes


    • HS diploma required 
    • Read, write and speak fluent English language.
    • 1-3 years applicable experience in GMP environment preferred
    • SAP experience a plus
    • 4 year degree preferered
    • Prior experience in planning, labeling, packaging, and shipping of clinical supplies and work experience in a regulated environment preferred.

    Addtional Needs - Quality Control and Knowledge of GMP/SOP compliance is a plus


    To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.


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