Senior Upstream Biologics Formulation Technician (cGMP)

RiseMe; St. Louis (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Annual bonus

Healthcare

Employee benefits

Job summary

Thermo Fisher Scientific in St. Louis, MO is seeking a Senior Formulation Technician to support commercial and clinical biologics manufacturing.

You will perform upstream (cell culture) activities, aseptic operations, and large-scale bioreactor work (50L–2000L) under cGMP guidelines. Responsibilities include executing batch records, maintaining logs and SOPs, and contributing to investigations and lean activities.

Qualifications

• Two years of experience in manufacturing, operation, or a lab setting.
• Experience in a cGMP environment preferred.

Responsibilities

• Execution of manufacturing batch records, work instructions and/or SOPs, with focus on proactive ‘right the first time’ executions. Assist with batch record reconciliation.
• Assist in all Department functions, such as maintaining suite, supplies, equipment, logbooks and data in accordance with site SOPs and policies.
• Documentation of all activities to meet cGMP requirements. Complete document reviews and revisions. Daily record review, tasks, and databases. Participate/Lead in shift exchanges, 1-1’s, meetings, attend meetings as needed to facilitate area needs based on changes, etc. (lean activities).
• Support a quality investigation by answering questions and making suggestions for improvement.
• Practices and promotes safe work habits and adheres to safety procedures and guidelines.
• Critical evaluation of processes, including foresight and thinking ahead.
• Ensure tasks are performed with a method of prioritization - interpret production schedules and complete tasks accordingly.

Skills

Critical thinking

Math skills

MS Office

Education

HS Diploma or equivalent

Job description

Thermo Fisher Scientific in St. Louis, MO is seeking a Senior Formulation Technician to support commercial and clinical biologics manufacturing.

You will perform upstream (cell culture) activities, aseptic operations, and large-scale bioreactor work (50L–2000L) under cGMP guidelines. Responsibilities include executing batch records, maintaining logs and SOPs, and contributing to investigations and lean activities.