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Senior Associate Material Coordinator / Senior Project Manager

Verista Inc.Indianapolis, IN
On-site Full-time $87.8K/yr - $136.2K/yr

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Experience Level

Senior

Qualifications

To be successful in this role, candidates should possess strong analytical skills, a detailed understanding of SAP processes, and experience in material coordination within a clinical manufacturing environment. Strong communication skills and the ability to work collaboratively with multiple teams are essential.

About the job

Job Overview

Verista is comprised of 500 dedicated professionals collaborating with some of the most esteemed brands in the life sciences sector to address their business challenges. Our mission is to stimulate growth and foster innovation within the scientific community, aiding researchers, organizations, and companies in tackling some of the most urgent healthcare issues worldwide. At Verista, we offer groundbreaking solutions and services that facilitate informed decision-making, stemming from our substantial investment in our team and their capabilities.

Our growth is propelled by exceptional individuals who thrive in a collaborative environment and align with our mission to assist life sciences clients in enhancing lives. Our talented and committed professionals aim to make a significant impact each day.

Company Culture and Values:

  • We empower and support our colleagues.
  • We commit to client success at every opportunity.
  • We have the courage to do the right thing.
  • We foster an inclusive environment where colleagues feel respected, engaged, and challenged.
  • We continuously develop new skills and learn from our experiences to enhance our collective expertise.

The Clinical Material Coordinator and SAP Process Owner will oversee the business processes involved in inputting molecules into SAP and managing material movement within internal clinical trial manufacturing sites as well as external collaboration partners. This includes logistics related to drug substance and product shipping, sample storage, and raw material coordination. This pivotal role will support manufacturing across the Product Research and Development (PRD) Organization. The Material Coordinator will act as the liaison for Clinical Manufacturing organizations to optimize communications with Clinical Supply and Delivery and the associated QA teams.

Key Responsibilities:

  • Develop SAP and business processes to support material movements, both physically and within SAP and Quality Systems for all PRD organizations.
  • Maintain SAP data related to orders to support the organization, which includes:
    • Establishing new materials and purchasing information aligned with sourcing decisions.
    • Creating new vendor and customer numbers as required.
    • Establishing Source Lists for triangulated sales products as necessary.
    • Overseeing MRP (Manufacturing Resource Planning) actions from the demand point.

About Verista Inc.

Verista Inc. is a leading consultancy in the life sciences industry, committed to solving complex business challenges through innovative solutions and dedicated expertise. Our team of professionals strives to enhance lives by empowering our clients and fostering growth in the scientific community.

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