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QA Final Product Release Specialist
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.
Your
missions :
Location: Lenexa, KS
| Job Summary and Purpose: |
The Final Product Specialist is responsible for review of documentation completed for production, testing, labeling and shipping veterinary vaccine products. Upon completion of review, the Final Product Specialist decides if the materials are suitable for use, release and shipping.
| Responsibilities and Key Duties: |
* People
o Must work with staff across multiple departments during review, correction and finalization of documentation.
o Responsible to work with production and QC groups to identify needed changes in documents or improvements in documentation.
* Quality
o Responsible for review of production and testing records for completeness and accuracy.
o Responsible for review of all materials used in the production of final products.
o Utilization of the JD Edwards computer system to set the appropriate disposition of materials.
* Delivery
o Responsible for maintenance of product tracking databases.
o Responsible for tracking and trending documentation errors.
| Core Competencies: |
* Shape solutions out of complexity - Is open and curious of others' perspectives
* Client focus - Has in mind clients' satisfaction
* Collaborate with empathy - Has a positive attitude towards collaboration
* Engage and develop - Clarifies short-term directions
* Drive ambition and accountability - Proactively manages own and others work
* Influence others - Communicates transparently
| Technical / Functional Competencies: |
* Strong interpersonal communication skills with all levels of management from production floor to senior management
* Exceptional attention to detail and ability to maintain consistency
* Strong organizational skills; able to effectively manage more than one priority and/or project at once
* Excellent communication skills, both written and verbal
* Proficiency in and knowledge of Microsoft Office Suite, Google Suite and other common computer applications
* Ability to work independently, with minimal supervision while adhering to deadlines
* Ability to perform data analysis, understand technical data and problem solve
* Must have flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary.
| Qualifications: |
Education - B.S. degree in a science related field (or adequate relevant experience) preferred
Work Experience - Minimum of two years' experience or demonstrated competency in a regulated biotech, or pharmaceutical industry environment. Experience working with records and document auditing is preferred.
Other - Knowledge of familiarity with quality systems
| Physical Requirements: |
* Able to read, write legibly and communicate in English
* Capable of working extensively with computers, and communicating with colleagues
* Able to communicate data both verbally and visually
* Tasks frequently require prolonged mental and visual concentration
| Working Conditions: |
* N/A
| Travel Required: |
* N/A
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.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
Your profile :
Education - B.S. degree in a science related field (or adequate relevant experience) preferred
Work Experience - Minimum of two years' experience or demonstrated competency in a regulated biotech, or pharmaceutical industry environment. Experience working with records and document auditing is preferred.
Other - Knowledge of familiarity with quality systems