Vaccine Process Transfer Technician

Ceva Santé Animale; Verona (AR); On-site; USD 60,000 - 80,000; Full time

Job summary

Ceva Animal Health is seeking a GID Technician in Verona, WI to assist in developing and transferring vaccine processes from lab to industrial scale. You will participate in industrialization strategies, batch preparation, risk assessments, and process improvement to support GMP-compliant production.

Responsibilities include performing laboratory work, assisting in technology transfer to Industrial Operations, ensuring quality standards, and maintaining accurate documentation under supervision.

Qualifications

• Education – BA/BS in Microbiology or Biology or Chemistry/Pharmacology or related areas of expertise.
• Work Experience – Minimum 2 years' work experience in aseptic processing, fermentation, cell culture, and assays in research and/or manufacturing environment is preferred.
• Other- Basic knowledge in Microbiology and Chemistry, tissue culture, and virus titration or prior virology experience a plus.

Responsibilities

• Assist in the industrial development, process, and product improvement of viral, bacterial, parasitic and/or recombinant vaccines of licensed and unlicensed vaccines.
• Oversees the manufacturing and/or analytical testing of development and first commercial batches.
• Industrialization Strategy Definition and Management: Executes the manufacturing & testing according to the industrial development and process transfer rationale to anticipate industrial needs.
• Batch Manufacturing Preparation: Orders, receives & identifies materials and components; manages inventory; tests feasibility at lab scale.

Skills

Process Transfer

GMP knowledge

Laboratory testing

Bioprocess

Quality standards

Education

BA/BS in Microbiology

Biology

Chemistry/Pharmacology

Job description

Ceva Animal Health is seeking a GID Technician in Verona, WI to assist in developing and transferring vaccine processes from lab to industrial scale. You will participate in industrialization strategies, batch preparation, risk assessments, and process improvement to support GMP-compliant production.

Responsibilities include performing laboratory work, assisting in technology transfer to Industrial Operations, ensuring quality standards, and maintaining accurate documentation under supervision.