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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.
Education
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)
Education
- High school diploma/GED minimally required.
- Associate's degree preferred but not required.
- 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 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
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