Job Description

Scientist I

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.

Your missions :

Location: Lenexa, KS


Job Summary and Purpose:




To function as a key contributor to the development and licensure of vaccines as well as new label claims or product improvement research of licensed vaccines. Ensure laboratory and clinical activities are performed in compliance with current scientific knowledge, quality and regulatory requirements. Support other departments for technical processes and organization.


Responsibilities and Key Duties:




Analytical


Independently perform a wide range of laboratory assays, such as classical microbiological techniques, general tissue culture, ELISA, Western blot, PCR, etc. Participate in development and validation of new analytical assays

Train other laboratory personnel in new techniques

Prepare data sets in spreadsheets for statistical analysis

Clinical


Organize and conduct/coordinate clinical trials

May act as a study monitor Prepare and process clinical samples

Communication


Independently source supplies in support of laboratory and clinical studies.

If required interacts with external collaborators in consultation with direct manager

Maintain regular inter and intradepartmental communication in support of ongoing projects

Present scientific literature for internal review
Scientific Writing/presentation


Maintain high quality laboratory documentation Author and edit laboratory methods, protocols, reports, and operating procedures of low to moderate complexity

Review technical documents for accuracy of timelines, methods, and data sets Prepare presentation using Microsoft PowerPoint for sharing of data
Laboratory Maintenance


Oversee the organization and maintenance of inventory records for freezers and contents

Oversee preparation of media, reagents, buffers and glassware used in laboratory tests

Set schedules and ensure completion of laboratory and equipment cleaning and maintenance

Adhere to appropriate safety requirements and protocols




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:




Working knowledge of microbiology techniques (aseptic technique, preparation of media, culturing organisms, etc.)

Experience performing laboratory assays Ability to participate in clinical trials

Ability to perform and interpret basic statistics Ability to design and propose experiments within one's scope of work

Ability to clearly and accurately write and present scientific information

Ability to work in a team setting




Qualifications:




Education - BA/BS in Microbiology, Biology, or related field





Work Experience - 5+ years of relevant experience, or a graduate degree (MS or PhD) in a related field


Other (consider certifications, specialized knowledge and/or training, etc.) Knowledge of virus propagation and titration techniques, experience in assay development and validation (e.g. PCR, ELISA, and Western blot), and experience using molecular techniques preferred





Physical Requirements:




Ability to read, write legibly, and communicate in English

Visual inspection




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

#USCEVA

Your profile :

Education - BA/BS in Microbiology, Biology, or related field


Work Experience - 5+ years of relevant experience, or a graduate degree (MS or PhD) in a related field


Other - Knowledge of virus propagation and titration techniques, experience in assay development and validation (e.g. PCR, ELISA, and Western blot), and experience using molecular techniques preferred