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.