Sr. Formulation Technician - 2nd Shift

Thermo Fisher Scientific • St. Louis, MO

4d • Onsite

About The Position

Thermo Fisher Scientific Inc. is seeking an individual with outstanding work behaviors to join our team as a Downstream Processing Technician III in St. Louis. This is a manufacturing role where you will have the opportunity to contribute to the production of world-class products that make a difference in people's lives. As a Downstream Processing Technician III, you will play a meaningful role in our ambitious mission to enable our customers to make the world healthier, cleaner, and safer. You will work closely with a team of proven professionals to compete in a fast-paced environment, ensuring flawless execution of downstream manufacturing processes.

Requirements

• HS Diploma/ GED required
• 2 years relevant work experience is required
• Able to read, write, and communicate in English
• Able to understand and carry out instructions
• Reliable
• 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
• Seeks and welcomes feedback and responds to coaching.

Nice To Haves

• bachelor's degree preferred
• Experience in cGMP environment preferred
• Knowledge of cGMP practices, aseptic techniques, or chemical concepts- preferred
• Subject Matter Expert on downstream processing steps
• Qualified to train other employees- preferred
• Qualified to train (preferred) and guide employees.

Responsibilities

• Execution of manufacturing batch records, work instructions and/or SOPs, with minimal instruction on a day-to-day basis and a focus on proactive ‘right the first time’ executions.
• Assist with batch record reconciliation.
• Able to complete 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. Daily record review, tasks, and databases.
• Complete preventative maintenance and work notifications tasks on time. Perform equipment testing and routine trouble-shooting.
• Oversee and perform timely consumption of materials and completion of quality documentation in appropriate systems
• Identify deviations, aid in investigations/root cause analysis, and provide input on major/critical deviations.
• Complete validation protocols with minimal supervision or direction.
• Schedule activities and coordinate the shift huddle in absence of the supervisor. Act as liaison with other groups within the manufacturing organization and a Subject Matter Expert on a variety of downstream processing steps techniques.
• Participate in shift exchanges, 1-1’s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities).
• Practices and promotes safe work habits and adheres to safety procedures and guidelines.
• Provides feedback on document revisions and/or document management including batch production records and manufacturing procedures.

Benefits

• Thermo Fisher Scientific Inc. is an equal opportunity employer and offers accessibility services for job seekers requiring accommodations in the application process. If you require an accommodation or assistance due to a disability, please contact us at 1-855-471-2255. We value diversity and are committed to crafting an inclusive and collaborative environment where all perspectives are valued.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED