Work Schedule
12 hr shift/nights

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Manufacturing Coordinator 1 - Nights

Location/Division Specific Information

St. Louis, MO / Drug Substance Division - This is one of the five divisions that make up the Pharma Services Group. We specialize in both small and large molecule development and commercial drug substance services. This allows us to serve the needs of Small/Emerging, Mid-Sized, and Large Pharma sectors globally!

• Ensure all consumables for production processes are accounted for upon delivery to stage process consumables in an organized manner for ease of use in production set-ups
• Assist with obtaining and placement of raw materials and consumables at/from the wipe-down station for entrance into the suite
• Collaborate with production support groups to ensure lines, kits, and assemblies are ready when needed within manufacturing and any missing components can be acquired timely.
• Ensure material kits are complete and available for manufacturing use prior to set up of process step. Confirm buffers are available prior to need. Ensure buffers move to the downstream manufacturing suites so production processing is not halted and on time processing needs are met

• Support ancillary tasks on the manufacturing floor such as fit and finish, material stock/supply and equipment staging.
• Assist with inventory counts within the production suites and coordinates results with Inventory Leads and Procurement.
• Performs or assists with investigations when discrepancies of inventory are discovered.
• Assist in all manufacturing process functions, such as maintaining suite, supplies with site SOPs and policies.
• Ensure tasks are completed with a method of prioritization - interpret production schedules and complete tasks accordingly.
• Participate in shift exchanges, 1-1's, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities).

• High school diploma or GED is required. Associates in a relevant scientific field preferred.

• 0-3 confirmed experience in a related field (regulatory cleaning/manufacturing preferred)
• Science experience related to pharmaceutical industry preferred.
• Must be a self-starter who can take general concepts and direction and produce desirable results.
• Basic knowledge of GMP/GLP regulations in cGMP/cGLP manufacturing environment preferred.

• Understanding 'why' and not just the 'how' of processes and practices
• Knowledge of cGMP practices, aseptic techniques, or chemical concepts seen as a plus

• Proficient with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS .
• Word and MS PPT is required.
• Inventory Management - SAP experience a plus.
• Time management and prioritization.

• Ability to read, write and speak English fluently.
• Ability to understand and carry out instructions.
• Good problem-solving and critical thinking skills.
• Excellent organization skills.
• Effective communication (written and verbal).