Manufacturing Technician - Batch & Fill; Verona, WI
Listed on 2026-07-08
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Manufacturing / Production
Manufacturing & Industrial Operations, Production QC/QA, Production Associate / Production Line
Location:
Verona, WI
Shift: Monday-Friday, 7:00 AM-3:30 PM
Job Summary and PurposeThe Lab Technician I supports laboratory operations by working directly with a variety of equipment including batching vessels, filling machines, and capping machines. This role involves handling inactivated bacterial and viral antigens, batching solutions, and semi‑finished products while adhering to aseptic techniques and current Good Manufacturing Practices (cGMP).
Responsibilities and Key Duties- Set up, operate, and perform turnaround of all processing equipment; includes working with chemicals, steam, compressed air, and pressurized vessels
- Operate batching vessels, filling machines, and capping machines
- Perform environmental monitoring during aseptic procedures
- Follow aseptic techniques during all applicable processes
- Conduct APHIS‑certified sampling procedures
- Operate general production equipment (e.g., autoclaves, pumps, scales, load cells, welders, sealers, particle monitors)
- Prepare chemical and biological solutions as required
- Perform daily cleaning and sanitation of labs and equipment
- Assemble batching and filling equipment for production processes
- Adhere to all SOPs and document activities in compliance with cGMP standards
- Maintain effective and professional working relationships across teams
- Comply with safety procedures and use appropriate personal protective equipment (PPE)
- Perform additional duties as assigned, including training others when capable
- Solutions out of Complexity – Adapt and respond effectively to dynamic lab environments
- Client Focus – Address internal and external needs with a balanced, solutions‑oriented approach
- Collaborate with Empathy – Share information openly and contribute meaningfully to team decisions
- Engage and Develop – Be open to learning, feedback, and knowledge sharing
- Drive Ambition and Accountability – Take ownership of work quality, timelines, and key performance indicators (KPIs)
- Influence Others – Communicate clearly and confidently with a structured and synthesized message
- Operate technical and computerized equipment (machine controls, instrumentation)
- Understand and follow primary production procedures and schedules; consult documentation when needed
- Learn and adhere to regulatory, health, safety, quality and environmental standards
- Utilize basic IT tools to support production tasks
- Apply lean manufacturing tools and support 5S and standard work practices
- Conduct basic analysis and problem‑solving; provide input to improvement initiatives
- Can provide basic coaching and apply lean tools as per 5S, standard work
- Understand production standards (e.g., time, materials, output targets)
- Contribute expertise to team projects as needed
- Strong writing, communication, and organizational skills
- Ability to work independently and as part of a fast‑paced team
- Effective planning and time‑management skills
Education:
Associate degree in a life‑science field, preferred
Work Experience:
1+ year experience in a cGMP environment preferred
Experience in a laboratory, scientific or animal‑handling field preferred
Other:
Familiarity with cGMP and CGLP procedures desirable
- Must be able to read, write legibly and communicate in English to understand safety instructions, procedures, and operational guidelines
- Must be able to squat, bend, and twist repetitively as part of the production process
- Must be able to stand for extended periods as needed for production activities
- Must be able to bend, stoop, push, pull and reach above shoulders
- Must be able to lift up to 25 pounds frequently and up to 50 pounds occasionally, following safe lifting procedures
- Must be able to perform visual inspection of products or materials to ensure quality and compliance
- Must be able to dress in and operate within cleanroom garments (e.g., gloves, gowns, masks, etc.) as required by safety and compliance protocols
- Must be able to perform repetitive wrist and shoulder rotations as part of the production process
- Must have sufficient manual dexterity to perform fine motor tasks, such as operating small tools or handling delicate materials
Clean room manufacturing laboratory: employees must follow strict hygiene protocols to maintain the controlled environment, including wearing cleanroom garments such as gloves, gowns, masks, and hairnets at all times to prevent contamination.
Travel RequiredNo travel required for this position.
Equal OpportunityCeva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
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