Production Tech 1-3rd Shift
Company: bioMerieux
Location: Chesterfield
Posted on: March 5, 2026
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Job Description:
The Production Technician I position is responsible for the
operation of high speed equipment used in the production and
packaging of VITEK 2 cards in a cGMP compliant manner. The position
may perform or assist in the setup, operation, inspection,
maintenance, troubleshooting and cleaning of equipment used
throughout the VITEK 2 Card Manufacturing and Packaging
processes.Additionally, this individual will be responsible for
completing production batches and corresponding documentation for
the associated tasks, AQL inspections, reworks and material
reconciliation that goes along with the batch.Contribute to
building a positive work environment. Primary Duties 1. Execute
production activities per approved Manufacturing Directions while
maintaining compliance with all job related SOPs. 2. Ensure that
all batch records are completed in an accurate, thorough, and
timely manner. 3. Execute validation protocols associated with
manufacturing/packaging equipment and procedures including
revalidation as required to maintain systems in a validated state.
4. Provide assistance with the review and revision of Manufacturing
Directions and SOPs necessary for the manufacture and packaging of
product. 5. Certified in operation of at least one high speed
manufacturing equipment efficiently and effectively, in some cases
highly automated, using HMI/SCADA interfaces. 6. Engage in
cage/rack movement, maintain product segregation, retrieve and
organize raw materials, and ability to learn fork truck operation.
7. Follow appropriate departmental cleaning procedures to ensure
adequate cleaning of the manufacturing areas. 8. Setup high speed
manufacturing equipment, within defined tolerances, to ensure
product runs are started on time and within established guidelines.
9. Comply with all safety policies and procedures at all times. 10.
Appropriately use PPE (Personal Protection Equipment) as required
to perform routine and non-routine duties. 11. Maintain all work
areas in a well-organized, clean and tidy manner at all times in
compliance with cGMP requirements. 12. Perform all work in
compliance with company quality procedures and standards. 13.
Performs other duties as assigned. Qualifications No experience
required; at least 1 year experience in FDA regulated manufacturing
environment and GMP is desired. Knowledge, Skills, and Abilities
Technical learning aptitude to quickly understand and acquire new
technical knowledge and skills. Attention to detail and the ability
to accurately interpret technical documentation are critical
Ability to perform computer applications including learning and
performing SAP transactions Ability to perform necessary
calculations and complex task sequences in order to meet production
requirements Written Communications - including the ability to
communicate technical data in written form Effective verbal
communication skills Effectively navigate social interactions in
the workplace Participate in a way that enhances team performance
and cohesion. Working Conditions and Physical Requirements Ability
to remain in stationary position, often standing, for prolonged
periods. Ability to ascend/descend stairs, ladders, ramps, and the
like. Ability to wear PPE correctly most of the day. Ability to
operate heavy machinery. Ability to adjust or move objects up to 50
pounds in all directions. Ability to stand for 8-12 hours. Ability
to work overtime as required to cover a 24/7 operation. Extensive
standing, repetitive hand and arm motions, ability to climb steps.
Must be able to push a wheeled cage that can weigh up to 600 lbs
fully loaded. Operating within cool temperature and low humidity
conditions within the production room.Constant noise is common due
to the operation of the air-dry chamber, taping and pouching
equipment. Excellent personal hygiene required.Appropriate gowning
requirements necessary for the production areas.Gloves are required
to handle the product. Hairnet, clean room gowns and/or lab coats
are required. Safety glasses and hearing protection are required
personal protective gear. Occasional environmental odors may be
prevalentThe estimated salary range for this role is between $17.50
and $19.50. This role is eligible to receive a variable annual
bonus based on company, team, and individual performance per
bioMerieux's bonus program. This range may differ from ranges
offered for similar positions elsewhere in the country given
differences in cost of living. Actual compensation within this
range is determined based on the successful candidate's experience
and will be presented in writing at the time of the offer.In
addition, bioMérieux offers a competitive Total Rewards package
that may include:·A choice of medical (including prescription),
dental, and vision plans providing nationwide coverage and
telemedicine options·Company-Provided Life and Accidental Death
Insurance·Short and Long-Term Disability Insurance·Retirement Plan
including a generous non-discretionary employer contribution and
employer match.·Adoption Assistance·Wellness Programs·Employee
Assistance Program·Commuter Benefits·Various voluntary benefit
offerings·Discount programs·Parental leavesbiojobsPandoLogic.
Category: , Keywords: Production Technician
Keywords: bioMerieux, O'Fallon , Production Tech 1-3rd Shift, Manufacturing , Chesterfield, Missouri