Core Technician I

About the role

The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical‑grade products. The core tech will also be responsible for maintaining, stocking, and set‑up of the clean‑room environment.

Responsibilities

• Participates in the Environmental Monitoring process as part of GMP production of viral therapies.
• Performs cell culture and product purification using aseptic technique when required.
• Coordinates EM equipment needs with the QC EM team for manufacturing processes.
• Drafts, completes, and revises manufacturing documents, including batch records and EM forms.
• Prepares buffers and components, including operation of a steam autoclave.
• Operates manual, semi‑automated, and automated equipment in support of routine clinical production.
• Operates environmental monitoring equipment such as Solairs, ApexZ50, and active counters.

Skills

• Aseptic technique and experience in cell culture and serological methods (preferred).
• Ability to pass Class 10,000 gowning qualification.
• Proficient with computer software, including Microsoft Office; strong organization, record‑keeping, project management, and time‑management abilities.
• Effective written and oral communication; team‑oriented, capable of independent work, and a strong work ethic.

Qualifications

• 1–3 years of relevant experience.
• Basic laboratory experience with a Bachelor’s degree, or intermediate laboratory experience within a cGMP clinical production environment combined with a high‑school diploma.
• Laboratory experience preferred.
• Bachelor’s degree in Life Sciences preferred.