Job Details
Job Title: Manufacturing Support Coordinator
Location: St. Louis, MO
Contract: 6 Months
Job Description:
How will you make an impact?
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/she will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to preparation and organization of the manufacturing suites.
What will you do?
Perform cleaning of manufacturing suites
Assist with delivery of raw materials and consumables to the manufacturing suites.
Ensure lines, kits, and assemblies are moved to the manufacturing suites to meet processing needs to prevent delay.
Confirm formulations are available prior to need. Ensure formulations move to manufacturing suites for production processing needs.
Support ancillary tasks on the manufacturing floor such as fit and finish, material stock/supply and equipment staging.
Participate in shift exchanges, 1-1 s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities).
How will you get here?
Education:
High school degree required. Associates in a relevant scientific discipline preferred.
Experience:
No experience required, but 1-3 years of relevant experience in a manufacturing and/or GMP environment preferred, preferably in pharmaceutical manufacturing.
Knowledge of cGMP practices seen as a plus
Professional Skills:
MS Office
Inventory Management SAP experience a plus.
Time management and prioritization
Detail oriented.
Results driven.
Abilities
Able to read, write, and communicate in English.
Able to understand and carry out instructions.
Organized
Reliable
Active communication (written and verbal)
Able to work in an environment of change.
Able to work independently and as part of a team.
Able to recognize problems developing, not just occurring.