Manufacturing Technician I - Batch & Fill (Verona, WI)

CEVA Logistics; Wisconsin; On-site; USD 45,000 - 65,000; Full time

Job summary

CEVA Logistics 在威斯康星州招聘制造技术员I，主要支持实验室运营。该职位要求操作多种设备并遵循无菌技术和良好生产规范。成功应聘者应具备生命科学领域的副学士学位，至少1年以上相关工作经验及对示范程序的熟悉。

Qualifications

• 具有在cGMP环境下工作的1年以上经验。
• 熟悉cGMP和CGLP程序。
• 倾向于有精益生产经验。

Responsibilities

• 设置、操作和处理所有加工设备。
• 在无菌程序中执行环境监测。
• 按照cGMP标准记录活动。

Skills

解决方案复杂

客户关注

同理心协作

推动雄心和问责

Education

生命科学领域的副学士学位

Job description

Manufacturing Technician I - Batch & Fill (Verona, WI)

公司的成功取决于与我们合作的充满激情的员工。

让我们一起分享才华。

作为动物保健领域的全球领导者，Ceva Animal Health 相信我们的成功与我们充满激情的员工息息相关，他们为所有动物研究、开发、生产和提供创新的健康解决方案，为我们这个多样化星球的未来做出了贡献。

我们致力于确保为农场动物（家禽、猪和反刍动物）、伴侣动物（狗和猫）以及野生动物提供最高水平的护理和福祉。

事实上，我们的 “护佑健康 与您同行”愿景强调人、动物和地球的健康与福祉是完全相互关联的。Ceva 比以往任何时候都更加致力于 “一体健康 ”的理念。

作为我们 “多元化、公平和包容 ”政策的一部分，Ceva Animal Heath 致力于雇佣残障人士，并将在整个面试过程中提供合理便利，以确保所有应聘者都能获得包容和无障碍的体验。如需申请便利，请联系Ceva人才招聘团队的成员。



您的任务 :

Location: Verona, WI

Job Summary and Purpose:

The 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

Core Competencies:

·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

Technical / Functional Competencies:

·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

Qualifications:

Education: Associate degree in 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 (consider certifications, specialized knowledge and/or training, etc.): Familiarity with cGMP and CGLP procedures desirable

Lean Manufacturing experience preferred

Physical Requirements:

·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.

Working Conditions:

Clean room manufacturing laboratory, where employees are required to follow strict hygiene protocols to maintain the controlled environment. This includes wearing cleanroom garments such as gloves, gowns, masks, and hairnets at all times to prevent contamination.

Travel Required:

This job description is intended to convey information essential to understanding the scope of the job and general nature and level of work performed by job holders within this job.This job description is not intended to be an exhaustive list of qualifications, skills, duties and responsibilities or working conditions associated with the job.This job description is not an employment contract.Ceva reserves the right to modify job duties and/or job descriptions at any time to meet the needs of the business.

*VEVRAA Federal Contractor

**Ceva 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 anyother characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.

669B

#USCEVA

您的简历:

Education: Associate degree in life-science field, preferred

Work Experience: 1+ year experience in a cGMP environment preferred
Experience in a laboratory, scientific or animal-handlingfield preferred

Other - Familiarity with cGMP and CGLP proceduresdesirable
Lean Manufacturingexperience preferred