Manufacturing Suite Coordinator II - Day Rotating Shift - B

ThermoFisher Scientific • Saint Louis, MO • 12h ago

Work Schedule

10 hr shift/days

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.)

Job Description

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location: St. Louis, MO

About the Role

The Manufacturing Coordinator plays a key role in supporting daily manufacturing operations by ensuring materials, equipment, and work areas are ready for execution. This position partners closely with Manufacturing, Supply Chain, and Quality teams to maintain production flow, support compliance, and ensure adherence to established processes and cadences within suite and BAM environments.

What You Will Do

Coordinate daily manufacturing activities to ensure material and operational readiness

Maintain gowning supplies across airlocks and production areas

Monitor and replenish suite-stocked materials (blue bins)

Perform routine inventory checks (including hydroxide counts) and update tracking systems

Ensure all required kits and materials are complete and staged prior to use

Support movement of buffers and materials across functional work areas

Inspect cold rooms for expired materials and escalate issues as needed

Review chain of custody reports and follow up on missing or delayed materials

Partner with supervisors and technicians to identify and address operational needs

Monitor production areas and coordinate movement of completed materials

Maintain cleanliness and organization of work areas, including MAL/PAL and core spaces

Execute end-of-shift cleaning and maintenance tasks

Perform routine walkthroughs to identify and document facility or process issues

Ensure training compliance and adherence to standard procedures

Minimum Qualifications

High school diploma or equivalent

1 year of experience in manufacturing, operations, or coordination roles or related field is required

Basic computer skills (Microsoft Office, Smartsheet or similar systems)

Strong communication skills (verbal and written)

Ability to multitask and manage priorities in a fast-paced environment

Strong interpersonal skills and ability to work cross-functionally

Good reading comprehension and ability to follow written procedures

High attention to detail and commitment to following standard processes

Ability to work independently and take initiative

Basic problem-solving skills and ability to escalate issues appropriately

Preferred Qualifications

Experience working in a GMP-regulated environment

Experience in manufacturing, operations, or coordination roles (biopharmaceutical preferred)

Familiarity with suite-based operations and/or BAM processes

Experience with SAP or other ERP systems

Key Competencies

Strong attention to detail and compliance mindset

Proactive and solution-oriented approach

Effective communication and teamwork

Ability to adapt in a dynamic, fast-paced environment

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