Biologics QC Operations Manager

Zoetis; Charles City (IA); On-site; USD 120,000 - 180,000; Full time

Job summary

Zoetis in Charles City, IA seeks a senior Quality Control leader to manage all QC operations and Animal Test facilities, ensuring vaccines meet US, EU and international regulatory requirements. You will oversee 4 QC departments, ensure product testing alignment with cGMPs, manage LIMS, and lead compliant documentation and regulatory inspections.

Responsibilities include directing test record reviews, coordinating schedules with manufacturing and planning, and driving regulatory readiness and

Qualifications

• BS/BA in science related field with 9-13 years of experience OR MBA/MS in science related field with 7-11 years of experience.
• Proficient in Microsoft Word, Excel, and PowerPoint, with the ability to leverage advanced features for data analysis, reporting, and presentation development.
• Strong written and oral communication skills
• Knowledge of USDA, EU, and Animal Welfare Act guidelines

Responsibilities

• Oversee day to day activities in the Quality Control laboratories and Animal Test facility.
• Advise Management of regulatory deficiencies and recommend appropriate regulatory actions when products do not meet Zoetis or government requirements.
• Actively participate in regulatory inspections of the Charles City facility.
• Direct the review of test records, batch records, SOPs, and validation protocols as necessary.
• Establish systems to assure audit readiness of testing documentation.

Skills

Leadership

Quality Control

Regulatory

cGMP

USDA/APHIS

Education

BS in science

MBA/MS in science

Tools

LIMS

Job description

Zoetis in Charles City, IA seeks a senior Quality Control leader to manage all QC operations and Animal Test facilities, ensuring vaccines meet US, EU and international regulatory requirements. You will oversee 4 QC departments, ensure product testing alignment with cGMPs, manage LIMS, and lead compliant documentation and regulatory inspections.

Responsibilities include directing test record reviews, coordinating schedules with manufacturing and planning, and driving regulatory readiness and