Production Support Technician I
Thermo Fisher Scientific

Job Info

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Job Description

Job Title: Manufacturing Technician 1 (Production Support- Facility Cleaning)

When you join us at Thermo Fisher Scientific, you will be part of a hard-working, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Location/Division Specific Information St. Louis, MO

The St Louis site is a fast-paced, 24/7 biologic drug substance manufacturing facility with approximately 800 employees; by year-end, we will be closer to 1k due to a site expansion project going on now. Overall, this GMP facility is focused on cell process development to support the clinical phase and commercial manufacturing by producing products to treat a variety of chronic health conditions, including cancers and other life-threatening diseases and COVID-19.

Shift Hours:

12-hour shift- 05:30am - 6:00pm, 3-2-2 schedule (Work Friday, Saturday and Sunday- Off Monday and Tuesday- Work Wednesday and Thursday. Schedule flips, Off Friday, Saturday and Sunday- Work Monday and Tuesday- Off Wednesday and Thursday)

Discover Impactful Work:

The candidate will be responsible for the daily cleaning of operations areas, routine and non-routine, in support of the manufacture of commercial and clinical biologics. These support activities consist of environmental cleaning per established standard operations procedures and in compliance with cGMP documentation practices.

A day in the Life:

Preparing for and execution of routine cleaning of manufacturing and support areas, per work instructions, and/or SOPs, with focus on "right the first time" executions.

• Complete tasks in order of prioritization
• Documentation of all activities to meet cGMP requirements. Maintain cGMP compliance in assigned work and follow all safety procedures, to include the use of Personal Protective Equipment.
• Complete preventative maintenance and work notification tasks on time, independently.
• Draft, review, and revise documents as necessary, SOP's, Logbooks, etc.
• Maintain up to date training assignments
• Participate in other required activities (perform safety inspections; participate in improvement projects, etc.)
• Participate in shift exchanges, 1-1's, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities)

Keys to Success:

Education

• High school diploma/GED minimally required.
• Associate's degree preferred but not required.

Experience

• 0-1 years of experience required.
• Experience in a clean room and/or GMP environment preferred.
• Ability to work independently on routine tasks, needing support to resolve complex issues.

Knowledge, Skills, Abilities

• Knowledge of cGMP practices seen as a plus
• Able to gown into and work in a clean room environment
• MS Office proficiency
• Strong prioritization skills
• Detail oriented
• Results driven
• Safety Attitude
• Able to read, write, and communicate in English
• Able to understand and carry out instructions
• Reliable
• Strong communication (written and verbal)
• Effectively multi-task
• 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
• Occasional heavy lifting or moving required

Must be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions or hair care products

This job has expired.