St. Louis, Missouri, United States of America
5 hours ago
Manufacturing Technician II

Work Schedule

12 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, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

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/Division Specific Information:
St. Louis, MO

United States

How Will You Make an Impact?:
The BAM Technician II is responsible for the routine performance of operations supporting the manufacture of commercial and clinical biologics. This role supports buffer and media formulation and environmental cleaning activities in accordance with established SOPs while maintaining strict compliance with cGMP documentation and safety practices.

A Day in the Life:
Prepare for and execute manufacturing batch records, work instructions, and SOPs with a strong focus on safety and right-first-time execution.

Weigh, transfer, and mix chemicals according to approved procedures.

Perform environmental cleaning and buffer/media formulation activities.

Document all activities in compliance with cGMP requirements.

Maintain cGMP compliance and follow all safety procedures, including proper use of personal protective equipment (PPE).

Complete preventative maintenance and work notification tasks on time.

Perform equipment testing and routine troubleshooting of process and analytical equipment.

Run in-process analytical testing as required.

Maintain raw material inventory using systems such as Kanban.

Maintain up-to-date training records.
 

Participate in safety inspections, improvement projects, and lean activities.

Participate in shift exchanges, 1:1s, and team meetings as needed to support operational demands.


Education:
High school diploma or equivalent required.

Experience:
1–3 years of relevant experience, or an equivalent combination of education and experience.

Experience with aseptic technique preferred.

Experience in a manufacturing and/or GMP environment preferred.



Knowledge, Skills, Abilities:
Understanding of processes with emphasis on the “why,” not just the “how.”

Knowledge of cGMP practices, aseptic techniques, and basic chemical concepts is a plus.



Physical Requirements / Work Environment
Occasional heavy lifting or moving of materials required.

Work performed in a manufacturing environment requiring adherence to safety and gowning requirements.



What We Offer:

Compensation
Competitive Pay
Performance Related Bonus where eligible
Annual merit performance-based increase

Excellent Benefits
Medical benefits
Paid Time Off/Annual Leave
Employee Referral Bonus
Career Advancement Opportunities

Confirmar seu email: Enviar Email