R&D Technician I
CEVA Logistics, Lenexa, KS, United States
Vos missions :
Provide essential support for the development and licensure of vaccines, expansion of label claims, and research aimed at improving existing products. Assist in laboratory and clinical activities while ensuring strict adherence to quality standards and regulatory requirements.
Location
Lenexa, KS
Support of Laboratory Activities
Execute laboratory assays with accuracy and consistency, following established SOPs, protocols, and quality standards.
Collect and document experimental data, ensuring completeness, accuracy, and data integrity.
Prepare media, reagents, buffers, solutions, and glassware required for routine and specialized laboratory procedures.
Maintain and propagate a variety of culture systems, including primary and secondary cells, immortalized cell lines, embryos, and bacterial cultures.
Assist in the organization, tracking, and maintenance of laboratory inventory, including freezer and consumable records.
Manage routine supply ordering and ensure timely availability of materials to support ongoing projects.
Perform routine equipment checks, coordinate maintenance needs, and ensure proper functioning of laboratory instruments.
Support laboratory safety and cleanliness by adhering to established cleaning schedules, waste management processes, and safety protocols.
Learn, adopt, and apply new laboratory techniques as required to support evolving research priorities.
Maintain high‑quality laboratory documentation, including accurate lab notebook entries, batch records, and electronic data logs.
Support of Clinical Activities
Assist in the execution and operational support of clinical studies in alignment with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Prepare, label, and organize materials, kits, and supplies needed for clinical trial procedures.
Process, handle, and document clinical samples with precision, ensuring compliance with chain‑of‑custody guidelines and quality standards.
Maintain accurate clinical documentation and contribute to the organization of study‑related materials.
Laboratory Maintenance
Maintain an organized, safe and efficient lab environment, including accurate records of inventory, supplies, and equipment status.
Ensure all media preparation, reagent preparation and cell culture activities adhere to established protocols and best practices.
Follow all safety guidelines, including proper use of PPE, hazardous material handling and adherence to regulatory and institutional requirements.
Participate in laboratory audits, safety inspections, and continuous improvement initiatives as needed.
Core Competencies
Shape solutions out of complexity
Client focus
Collaborate with empathy
Engage and develop
Drive ambition and accountability
Influence others
Technical / Functional Competencies
Experience in microbiology techniques, including aseptic handling, media preparation, and organism culturing.
Familiarity with a variety of laboratory assays and related methodologies.
Ability to contribute effectively to clinical trial activities in compliance with protocols.
Written and verbal communication skills in English, with the ability to produce clear and accurate documentation.
Competence in performing experiments within defined scope and following established procedures.
Skilled in preparing and presenting scientific information clearly and accurately.
Demonstrated ability to collaborate and work effectively in a team‑oriented environment.
Qualifications
Education: Associate’s degree in microbiology, biology or related field with 2 years of relevant experience or BA/BS in microbiology, biology or related field.
Work Experience: Background in aseptic techniques, cell culture, and animal handling is preferred.
Physical Requirements
Visual inspection: Tasks frequently require prolonged mental and visual concentration.
Able to lift 50 lbs.
Working Conditions
May use hazardous chemicals to complete tasks.
Work in laboratory and animal facility setting using required personal protective equipment.
Travel Required
N/A
Other Information
This job description is intended to convey information essential to understanding the scope of the job and the 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.
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Provide essential support for the development and licensure of vaccines, expansion of label claims, and research aimed at improving existing products. Assist in laboratory and clinical activities while ensuring strict adherence to quality standards and regulatory requirements.
Location
Lenexa, KS
Support of Laboratory Activities
Execute laboratory assays with accuracy and consistency, following established SOPs, protocols, and quality standards.
Collect and document experimental data, ensuring completeness, accuracy, and data integrity.
Prepare media, reagents, buffers, solutions, and glassware required for routine and specialized laboratory procedures.
Maintain and propagate a variety of culture systems, including primary and secondary cells, immortalized cell lines, embryos, and bacterial cultures.
Assist in the organization, tracking, and maintenance of laboratory inventory, including freezer and consumable records.
Manage routine supply ordering and ensure timely availability of materials to support ongoing projects.
Perform routine equipment checks, coordinate maintenance needs, and ensure proper functioning of laboratory instruments.
Support laboratory safety and cleanliness by adhering to established cleaning schedules, waste management processes, and safety protocols.
Learn, adopt, and apply new laboratory techniques as required to support evolving research priorities.
Maintain high‑quality laboratory documentation, including accurate lab notebook entries, batch records, and electronic data logs.
Support of Clinical Activities
Assist in the execution and operational support of clinical studies in alignment with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Prepare, label, and organize materials, kits, and supplies needed for clinical trial procedures.
Process, handle, and document clinical samples with precision, ensuring compliance with chain‑of‑custody guidelines and quality standards.
Maintain accurate clinical documentation and contribute to the organization of study‑related materials.
Laboratory Maintenance
Maintain an organized, safe and efficient lab environment, including accurate records of inventory, supplies, and equipment status.
Ensure all media preparation, reagent preparation and cell culture activities adhere to established protocols and best practices.
Follow all safety guidelines, including proper use of PPE, hazardous material handling and adherence to regulatory and institutional requirements.
Participate in laboratory audits, safety inspections, and continuous improvement initiatives as needed.
Core Competencies
Shape solutions out of complexity
Client focus
Collaborate with empathy
Engage and develop
Drive ambition and accountability
Influence others
Technical / Functional Competencies
Experience in microbiology techniques, including aseptic handling, media preparation, and organism culturing.
Familiarity with a variety of laboratory assays and related methodologies.
Ability to contribute effectively to clinical trial activities in compliance with protocols.
Written and verbal communication skills in English, with the ability to produce clear and accurate documentation.
Competence in performing experiments within defined scope and following established procedures.
Skilled in preparing and presenting scientific information clearly and accurately.
Demonstrated ability to collaborate and work effectively in a team‑oriented environment.
Qualifications
Education: Associate’s degree in microbiology, biology or related field with 2 years of relevant experience or BA/BS in microbiology, biology or related field.
Work Experience: Background in aseptic techniques, cell culture, and animal handling is preferred.
Physical Requirements
Visual inspection: Tasks frequently require prolonged mental and visual concentration.
Able to lift 50 lbs.
Working Conditions
May use hazardous chemicals to complete tasks.
Work in laboratory and animal facility setting using required personal protective equipment.
Travel Required
N/A
Other Information
This job description is intended to convey information essential to understanding the scope of the job and the 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.
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