GMP Laboratory Technician: Cell Culture, Fill/Finish

Sunrise Systems, Inc.; Houston (TX); On-site; USD 42,000 - 70,000; Full time

Job summary

Sunrise Systems, Inc. is seeking a skilled technician to participate in aseptic processing of clinical-grade products, including cell culture, purification, formulation, and filling activities. You will also help maintain and stock clean room environments and support GMP production of viral products.

The role involves drafting and revising manufacturing documents, preparing buffers, and assisting in validation and troubleshooting of equipment. Strong communication and organization are essential.

Qualifications

• Bachelor's or associate's degree required.
• Experience with aseptic techniques preferred.
• Experience in cell culture and serological methods preferred.
• Ability to pass Class 10,000 gowning qualification.
• Strong written and oral communication; team-oriented and independent work skills.
• Proficiency with Microsoft Office and good record-keeping.

Responsibilities

• Participate in aseptic processing of clinical-grade product.
• Participate in GMP production of viral products.
• Cell culture and column chromatography using aseptic techniques.
• Draft, complete, and revise manufacturing documents (Batch Records, Specifications, Forms, Change Controls, Deviations, SOPs).
• Buffer and component preparation, including operation of steam autoclave.
• Fill/finish of viral products and cell banking.
• Assist in validation, changeover, data collection, and troubleshooting of process equipment.

Skills

Aseptic technique

Cell culture

Process purification

Documentation management

Time management

Team collaboration

Education

Bachelor's or Associate's degree

Tools

Microsoft Office

Job description

Sunrise Systems, Inc. is seeking a skilled technician to participate in aseptic processing of clinical-grade products, including cell culture, purification, formulation, and filling activities. You will also help maintain and stock clean room environments and support GMP production of viral products.

The role involves drafting and revising manufacturing documents, preparing buffers, and assisting in validation and troubleshooting of equipment. Strong communication and organization are essential.