Quality Scientist II — Vaccine QC & Analytical Testing

zoetis; Charles City (IA); On-site; USD 65,000 - 85,000; Full time

Job summary

Zoetis in Charles City, IA seeks a Quality Scientist II to execute cGMP-compliant quality testing for vaccines and antigen stocks. The role involves constructing and testing using egg-based methods, supporting qualification/validation, transfers, and related projects in the QA/QC labs.

The candidate will perform analyses for incoming, in-process, and finished goods, write SOPs, participate in investigations, and ensure documentation is maintained. Collaboration across departments is essential.

Qualifications

• Knowledge of cGMP/GLP requirements.
• Proficient with Microsoft Word, Excel, and PowerPoint.
• Ability to work independently and as part of a team.
• Strong attention to detail.

Responsibilities

• Testing of samples from manufacturing to ensure Quality and compliance.
• Analyses including extraneous, sterility, stability, inactivation, and potency testing.
• Maintain testing schedules with minimal direction.
• Execute and report validation studies.
• Write and revise SOPs and standard methods.
• Support investigations using DMAIC process.
• Clean and maintain lab equipment and facilities.
• Navigate QC software packages used during routine work.
• Prepare media and reagents.
• Participate in Media Fill inspections.
• Monitor lab equipment and performance.
• Maintain cGMP documentation and execute written procedures.
• Work effectively in a team and communicate across departments.

Skills

cGMP/GLP

MS Office

Attention to detail

Independent worker

Education

BS/BA in science

Tools

Laboratory software

Job description

Zoetis in Charles City, IA seeks a Quality Scientist II to execute cGMP-compliant quality testing for vaccines and antigen stocks. The role involves constructing and testing using egg-based methods, supporting qualification/validation, transfers, and related projects in the QA/QC labs.

The candidate will perform analyses for incoming, in-process, and finished goods, write SOPs, participate in investigations, and ensure documentation is maintained. Collaboration across departments is essential.