The Lab Technician II provides support in the manufacture of synthetic RNA vaccines through performance in making RNA to filling of final product and diluent.

* Prepare solutions and equipment

* Produce upstream bulk/antigen in accordance with standard operating procedures (SOP's)

* Conduct filling of vaccine and diluent

* Run label line for labeling vaccine

* Maintain inventory of supplies physically and in JDE

* Launch work orders in JDE for solutions and batch records, as needed

* Cleaning of laboratories and equipment

* Perform duties in accordance with standard operating procedures

* Assist in the transfer, as needed, of the SRV platform to the Ceva Verona location.

* Assist in the maintenance of the SRV procedures, batch records, and assist in implementation of new or improved processes as needed.

* Accurately complete all necessary documentation in accordance with good documentation practices

* Train junior staff, as needed

* Additional duties as assigned

* Shape solutions out of complexity - work to evolve immediate environment

* Client focus - Make sure needs and requests are treated equally and in a positive way

* Collaborate with empathy - Fully takes part in the working group to share information, listens to others and have a clear idea of the decisions taken

* Engage and develop - Open to share knowledge and receive feedback from others

* Drive ambition and accountability - Ensure accuracy of work with the use of KPI's and responsible commitment

* Influence others - Show structure and confidence while speaking and guiding others

* Strong mathematical aptitude

* Good verbal and written communication skills

* Ability to work overtime as needed

* Knowledge and practice of aseptic technique and clean room behavior

* Knowledge of Microsoft office

* Follow all relevant department policies, procedures, SOPs, and other requirements during project execution

Education -

* Bachelor's degree in a biological science field (i.e. microbiology, virology, biochemistry, molecular biology, or immunology) required

Work Experience -

* Two or more years of laboratory experience required, or a combination of education and experience

* Experience working in aseptic production environments required

* Experience in FDA or EU GMP regulated environment desired

Other (consider certifications, specialized knowledge and/or training, etc.) - A working knowledge of microbiology, molecular biology and/or biochemistry; additional experience in related areas of biologics production, quality control, quality assurance and/or research desired.

* Able to read, write legibly, and communicate in English

* Standing for long periods of time

* Frequent repetitions of bending, twisting, lifting arms above head, wrist and shoulder movements

* Visual inspection

* Dexterity: Frequent fine motor movement

* Lifting up to 50 lbs

* Daily dressing and operating in clean room required garments and PPE

* Clean room manufacturing laboratory in dedicated and sterile full suit gowns, including face mask

* 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