Core Technician I

Responsibilities:

• Participates in the Environmental Monitoring process as part of GMP production of viral therapies
• Cell culture and product purification using aseptic technique when required
• Coordinates EM equipment needs with QC EM team for Manufacturing processes
• Drafting, completion and revision of manufacturing documents including Batch Records and EM forms
• Buffer and component preparation including operation of steam autoclave
• Operation of manual, semi-automated and automated equipment in support of routine clinical production
• Operating Environmental monitoring equipment such as Solairs, ApexZ50, active counters

Requirements:

• Aseptic technique and experience in cell culture and serological methods preferred
• Able to pass Class 10,000 gowning qualification
• Computer software skills including Microsoft Office, organization skills, recordkeeping skills, ability to manage multiple projects, time management skills.
• Written and oral communication skills, team oriented, independent work skills, strong work ethic
• 1-3 Years Experience
• Basic Lab experience with a Bachelor's degree or Intermediate Lab experience within a cGMP clinical production environment and a High School Diploma.
• Lab experience preferred.
• Bachelor's Degree in Life Sciences preferred