• Coordinates and performs activities associated with daily lab operations including buffer preparation, environmental monitoring, equipment maintenance, lab maintenance (lab and labware cleaning), inventory of chemicals and document review. .• Writes internal reports, updates batch records.• Works with potentially hazardous materials.Experience:• 3 years of laboratory experience or equivalent• Demonstrates the knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Good Laboratory Practices (GLP).• Must be flexible and demonstrate the ability to switch priorities to meet business needs.• Associate degree in Life Science or related discipline is a plus.• Must be able to work in a fast-paced GMP regulated manufacturing environment working with time sensitive projects.• Verbal and written communication skills.• Computer and math skills.• Must be proficient with MS Outlook, Word, and Excel.• Capable of prioritizing daily work, and able to work both independently as well as with the team.Shift time :6:00 am to 2:30 pmVIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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