Scientist I - Genomics

The Molecular Research Scientist I works with the Genomic Platforms team. The Scientist will manage the molecular aspects of the Respons Prescription SRV program and supports the overall program goals and strategy of the group which will include significant laboratory activities such as the synthesis of pathogen target genes and construction and assessment of SRV candidates. The Scientist will also amplify large quantities of DNA to be used in SRV production. The Scientist will also assist with USDA submissions and on-site audits.

• Respons Prescription implementation and laboratory management.
• Designing and ordering genes of interest (sequences supplied).
• Synthesizing and cloning new genes into the Response vector plasmid.
• Screening clones to identify 100% accurate plasmids.
• Amplifying and purifying DNA for new MSQs.
• Appropriately uses and maintains lab equipment. Ensures safe removal of waste. Manages lab needs (i.e. reagent supply).
• Prepares, purifies, qualifies and labels reagents for experiments and continuously monitors the stock.
• Ensures proper documentation and recording of the test in the lab journal and/or electronic database.
• Respons Prescription MSQ DNA release testing.
• Carries out routine analytical assays accurately. Strictly adheres to lab methodologies and protocols.
• Calculates results.
• Generates Certificate of Quality for each MSQ.
• Compliance
• Maintaining accurate inventories for all long-term bacterial storage samples and MSQ DNA stored at GIC.
• Ensures proper documentation of R&D related activities and assays.
• Contributes to SOP writing and complies with all related activities and assays.
• Stores and manages samples, strictly following R&D rules.
• Molecular cloning and DNA analysis techniques (e.g. bacterial transformation, nucleic acid purification, restriction enzyme digest, gel electrophoresis, spectrophotometric analysis, Next Generation Sequencing).
• Overseeing/organizing shipment of MSQ DNA to Verona.
• Assist with USDA submissions and on-site audits.

* Drive ambition and accountability - shows concerns for reaching targets; ensures the accuracy of his/her own work using KPIs and a responsible commitment

* Influence others - communicates clearly

* Engage end develop - values learning for oneself and others

* Collaborate with empathy - Response to cooperation requests. Fully participates in the working group to share information and work with others

* Client focus - responds appropriately to needs and requests

* Shape solutions out of complexity - accepts the need for flexibility. Works and evolves with his/her immediate environment

• Communication and presentation skills - verbal, written communication and capacity to crate impactful presentations, clear documentation (Fundamental)
• Scientific knowledge to be able to make technical decisions for development and to interpret results (Fundamental)
• Molecular biology techniques and assays
• Scientific writing - (Fundamental)
• Analytical skills - knowledge of molecular biology test methods: (Fundamental)
• Regulatory & Quality knowledge (Fundamental)
• Project Management (Fundamental)

* Strong ability to work independently and develop an expanding technical and theoretical knowledge base

Education - Requires a MS in Molecular Biology, Cell Biology, Immunology, Virology or related field, or BS with relevant laboratory experience, PhD degree considered a plus

Work Experience - Three years relevant laboratory experience in industry or academia is preferred; focus on molecular cloning, analysis, and sequencing.

Other (consider certifications, specialized knowledge and/or training, etc.) -

• Proficiency in aseptic techniques
• Detail oriented with an ability to independently record scientific progress
• Understand molecular and cellular biology techniques. Previous experience with virology and viral vector construction as an alternative.

N/A

N/A

< 5% time spent traveling

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

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