Manufacturing Technician I - Nucleotide - Monday-Friday 6:00AM-2:30PM

CEVA Logistics; Wisconsin; On-site; USD 35,000 - 50,000; Full time

Job summary

Ceva Logistics 在威斯康星州 Verona 招聘一位制造技术员 I，专注于合成 RNA 疫苗的生产。该职位涉及设备准备、支持生产流程和執行标准操作程序。理想候选人应具备相关工作经验和科学背景，可以在快节奏的环境中独立工作，确保产品的质量和安全。加入这样一家研发驱动的创新公司，为动物健康行业的未来贡献您的力量。

Benefits

健康保险

401(k) 计划

带薪休假

Qualifications

• 至少有一年在 cGMP 环境中的工作经验，优先考虑。
• 相关的科学或动物领域工作经验或实验室经验者优先。
• 对 cGMP 和 CGLP 程序的知识是可取的。

Responsibilities

• 在指导下准备设备和溶液。
• 支持上游生产流程，并遵循操作规范。
• 参与疫苗和稀释剂的填充操作。
• 遵循认证取样程序，执行清洁和消毒任务。
• 记录所有活动，并遵守 cGMP 要求。

Skills

沟通技巧

团队合作

操作设备能力

遵循规定能力

细节关注

Education

中学文凭或 GED

生命科学领域的学士或副学士学位

Tools

实验室设备

Job description

Manufacturing Technician I - Nucleotide - Monday-Friday 6:00AM-2:30PM

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

SHIFT: MONDAY-FRIDAY, 6:00AM-2:30PM

Job Summary and Purpose:

The Lab Technician I will support in the manufacture of synthetic RNA vaccines through performance in making RNA to filling of final product and diluent.

Responsibilities and Key Duties:

·Assist with preparation of equipment and solutions under guidance

·Support upstream production processes in accordance with SOPs

·Participate in filling operations for vaccine and diluent

·Operate standard production equipment (e.g., autoclaves, pumps, pH meters, labeling)

·Follow certified sampling procedures after training

·Prepare solutions and equipment

·Perform scheduled cleaning and sanitation of lab spaces and equipment

·Assemble and disassemble equipment for production tasks

·Record all activities accurately in compliance with cGMP requirements

·Follow established inventory control practices; update JDE as directed

·Wear required PPE and follow all safety protocols

·Adhere to SOPs and contribute to a safe, organized work environment

·Assist in the maintenance of procedures, batch records, and assist in implementation of new or improved processes as needed

·Collaborate effectively with peers and supervisors

·Participate in cross-training and ongoing skill development

·Perform other duties as assigned to support production

Core Competencies:

·Shape solutions out of complexity – Work to evolve within immediate environment

·Client focus - Make sure needs and requests are treated equally and in a positive way

·Collaborate with empathy - Fully take part in the working group to share information, listen to others and have a clear idea of the decisions taken

·Engage and develop - Open to share knowledge and to receive feedback from others

·Drive ambition and accountability - Ensure accuracy of work with the use of KPI's and a responsible commitment

·Influence others -Show structure, confidence while speaking and guiding others

Technical / Functional Competencies:

·Able to operate technical machinery and possibly computerized equipment (machine controls and instrumentation)

·Know main production procedures on equipment as qualified and consult documentation if needed

·Able to follow instructions and production schedules

·Understand all regulations (health/safety, quality and environment standards) applicable to scope

·Can use main IT tools to perform his/her job in production

·Understand lean philosophy and purpose

·Can apply performance management tools per KPI follow-up

·Apply basic lean tools as per 5S, standard work

·Ability to consider production standards (time, raw materials/ productivity, final quantity)

·Actively contributes to projects and provides input

·Excellent writing and communication, interpersonal and organization skills

·Knowledge and practice of aseptic technique and clean room behavior

·Must be able to work both independently and in a fast-paced team environment

Qualifications:

Education

·High School Diploma or GED required, Bachelor/Associate degree in life-science field, preferred

Work Experience

·Minimum of one-year in a cGMP environment, preferred

·Related scientific, animal field work experience or experience in lab environment, preferred

Other (consider certifications, specialized knowledge and/or training, etc.)

·Knowledge of cGMP and CGLP procedures is desirable; Experience with Lean Manufacturing is preferred

Physical Requirements:

• Ability to read, write, and communicate effectively in English.
• Prolonged periods of standing, as well as occasional bending, stooping, pushing, pulling, reaching above shoulders, and stretching.
• Ability to lift and carry up to 25 pounds frequently, and up to 50 pounds occasionally.
• Hand-eye coordination and manual dexterity sufficient to operate laboratory equipment, including manual valves and other tools.
• Ability to perform visual inspections with or without corrective lenses.
• Daily use of personal protective equipment (PPE) and adherence to cleanroom garment requirements.

Working Conditions:

·Clean room manufacturing laboratory in dedicated sterile gowning and PPE

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.

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您的简历:

Education
High School Diploma or GED required, Bachelor/Associate degree in life-science field, preferred

Work Experience
Minimum of one-year in a cGMP environment, preferred
Related scientific, animal field work experience or experience in lab environment, preferred

OtherKnowledge of cGMP and CGLP procedures is desirable; Experience with Lean Manufacturing is preferred