Receiving Associate

Corin•Raynham, MA

13h•$19

About The Position

Corin is recruiting for a Receiving Associate to join the team on temporary to permanent basis. The key element of this role is to coordinate the efficient receipt, storage, movement to quality, and distribution of all materials delivered to Corin’s Distribution Center in Raynham, MA. The key results are: Prompt receipt and processing of all incoming packages Updating and maintaining SAGE (ERP system) where all transactions are tracked Clear and tidy workspace

Requirements

A high school diploma, GED, or equivalent
Computer literacy - can send professional emails, basic Excel skills and read key documentation
A can-do attitude - if you are keen, motivated, reliable and not afraid to work hard
Willing and able to lift objects to 25lbs
Worked in a Warehouse environment previously
Good manufacturing practice experience preferably
Strong computer skills: Excel experience required; ERP experience strongly preferred
The ability to work as part of a team but take ownership of individual tasks
Strong communication skills, both written and verbal

Nice To Haves

Warehouse, distribution or logistics experience would be an advantage but the above is more important to us.
Previous experience within a managerial or leadership role.
Medical device industry experience would be an advantage
Previous knowledge of Sage would be advantageous

Responsibilities

Receipt and process all deliveries including booking onto the SAGE stock system
Ensure stock accuracy on all stock control software
Ensure good housekeeping of the work area
Support distribution and loaner as requested
Support in all other goods Inwards tasks and functions as and when required to include: Receipt, inspect, and provide appropriate storage for all medical device final packaging material
RMA Processing
Process expired goods that have been returned
Prepare production material paperwork and issue it to the shop floor
Adhere to Quality Management System (QMS) requirements in line with Corin’s ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820.
Ensure that process and timeline requirements for Corrective & Preventive Actions (CAPA) are met by Corin’s Standard Operating Procedures (SOPs) and in support of Corin’s Global Objectives for CAPA.