QA Technician I (Verona, WI)

QA Technician I (Verona, WI)

The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Yourmissions :

Location : Verona, WI

Job Summary and Purpose :

Responsible for assuring the consistent quality of products and services by examining and reporting on the adequacy and / or deficiencies associated with documentation created during manufacturing and testing activities from receipt of inbound materials to final product shipment. This position will also support and assist with the day-to-day administration of the company's quality systems and document control programs.

Responsibilities and Key Duties :

• Review records and data for accuracy and adherence to internal procedures, good manufacturing practices, and regulatory requirements; using a guided processes for direction
• Conduct authorized sampling of final products
• Schedule and coordinate processing of final product samples for shipment
• Maintain inventory of final product retention samples and final product stability samples
• Understand and apply the Quality Management System (QMS) procedures and policies
• Issue records for process execution
• Perform release of inbound materials and in-process materials using the guided process
• Record and track data for trending and / or evaluation
• Update and maintain tracking log systems
• Assist with the administration of quality documents and the document control system
• Assist with the organization and maintenance of quality department files
• Explain and role model the expected 'quality behaviors' on the shopfloor

Core Competencies :

Technical / Functional Competencies :

Qualifications :

Education - Bachelor's degree in biological science or Quality Management System (QMS), preferred, or Associates degree plus equivalent work experience

Work Experience - Minimum of one year of experience, preferred or demonstrated competency in a regulated biotech, or pharmaceutical industry environment. Experience with record and document auditing, preferred

Physical Requirements :

Working Conditions :

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.

669B

USCEVA

Yourprofile :

Education - Bachelor's degree in biological science or Quality Management System (QMS), preferred, or Associates degree plus equivalent work experience

Work Experience - Minimum of one year of experience, preferred or demonstrated competency in a regulated biotech, or pharmaceutical industry environment. Experience with record and document auditing, preferred