Within this role you will be a key member of an External Manufacturing Team who collaborates with various departments and manufacturing partners to ensure timely delivery of materials and on-time production and release of parenteral medicines.

This role works with minimal direction, proactively identifies and resolves issues that could impact production schedules and is capable of identifying and implementing meaningful change.

As an Associate Materials Specialist a typical day might include, but is not limited to, the following :

Acting as the subject matter expert for Oracle to process CMO Quotes (Project Plans / Work Orders) and invoices, tracking the status of PO approval

Maintaining critical data databases and ensuring accuracy and integrity of the data

Generating reports vital to manage production activities and provides input on key decisions

Tracking, trending and supervising information and data; preparing reports and analysing operations data

Identifying issues and taking the initiative to resolve them

Collaborating with Supply Chain Logistics in coordinating shipments and ensures timely deliveries

Ensuring accessible history of allocations, knowledge of material consumptions and calculates manufacturing yields in Oracle and other designated systems

Coordinating logistic documentation enabling shipments

This role might be for you if :

You demonstrate proficient skills in Excel, PowerPoint, Visio, Word, etc. in addition to experience working within shared work environments

You have strong interpersonal, written and oral communication skills

You show resilience and flexibility

To be considered for this opportunity you should have a BS / BA in scientific discipline and 0-2 years of related experience in cGMP manufacturing operations (clinical and / or commercial External Manufacturing) or equivalent combination of education and experience.

IREADV #JOBSIEPR #LI-Onsite

Last updated : 2024-05-24