Associate QC Systems Specialist

Zoetis Spain SL; Charles City (IA); On-site; USD 60,000 - 90,000; Full time

Job summary

Zoetis is seeking an Associate QC Systems Specialist to serve as SME for QC digital systems such as SAP, zLIMS, Binocs, and Veeva Vault. The role focuses on maintaining accurate master data and upholding biological testing specifications to ensure regulatory compliance.

You will work with Production, QA, Regulatory, GMT and Supply Chain to prioritize tasks, improve systems, and support continuous improvement as a self-starter. Strong communication and teamwork are essential.

Qualifications

• BA/BS in scientific discipline or business with 0–2 years experience (SAP/zLIMS experience highly desired).
• Strong communication, interpersonal and leadership skills.
• Ability to interact positively with colleagues at all levels, including senior leadership.

Responsibilities

• SME for QC digital systems including SAP, LIMS, Binocs, and Veeva Vault.
• Maintain current biological testing specifications and master data accuracy in the system.
• Ensure compliance with regulations including 9CFR and European Pharmacopeia; support sample receipt and stability testing.
• Maintain appropriate cGMP documentation and follow Zoetis Quality Standards, Policies and Procedures.

Skills

Microsoft Word

Excel

PowerPoint

Outlook

Veeva Vault

SAP

LIMS

zLIMS

Education

Bachelor's degree in scientific discipline or business

Tools

SAP

zLIMS

Job description

Role Description Position Summary: The Associate QC Systems Specialist acts as the QC Systems (SAP, zLIMS, Binocs and other digital systems for QC) subject matter expert. Maintains compliance through creation and maintenance of biological product specifications, ensuring the master data is accurate in the system,20-08 template accuracy, troubleshoots and participates with global teams to provide feedback, and support continuous improvement, . The successful candidate must be a self-starter and have the ability to prioritize work based on the needs of Production, Quality Assurance, Quality Control, Regulatory, GMT and Supply Chain.

Position Responsibilities: Subject Matter Expect (SME) for the QC digital systems including but not limited to SAP, LIMS, Binocs, and Veeva Vault Maintain current and initiate new biological testing specifications as required to ensure compliance Working knowledge of regulations for testing of biological products; including 9CFR and European Pharmacopeia Cross functional role within the Quality Control office area to support 2008/2020/CofA preparation and sample receipt/dispersal along with ensuring on time stability testing. Maintain appropriate departmental cGMP documentation. Follow all Zoetis Quality Standards, Policies and Procedures

Education and Experience: BA/BS degree in scientific discipline or business with 0-2 years experience (experience in SAP/zLIMS highly desired) or 8 years relevant experience. Demonstrated commitment to the Zoetis Core Beliefs and leadership competencies. Demonstrated ability to interact positively with all levels of colleagues including senior leadership. Demonstrated ability to achieve results. Strong communication (oral and written), interpersonal, and team/group interactive and leadership skills. Strong commitment to product quality, customer service, and continuous improvement.

Technical Skills Requirements: Proficient in Microsoft Word, Excel, PowerPoint, Outlook, ETS, Veeva Vault and SAP, LIMS Experience with 9CFR & EU regulatory requirements. Understanding of Outlines of Production/Special Outlines

Physical Requirements: Must be able to walk, sit, or stand for long periods of time. Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently. Must be able to work scheduled 40 hours with the ability to work overtime as needed. Frequent lifting and carrying of 5 to 50lbs. Regular reaching, bending, stooping, and twisting. Repetitive motion and substantial movement of the wrists, hands, and/or fingers. Full time Regular Colleague

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at [e-mail] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act.

All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact.

At Zoetis, our purpose is to nurture our world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues’ careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources.