3rd Shift Cell Therapy Production Associate (GMP)

Orcabiosystems; Sacramento (CA); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Pre-IPO equity

Annual bonus

Medical, dental, vision benefits

PTO

401(k)

Life and disability coverage

Parental leave

On-site lunches

Job summary

Orca Bio operates a Sacramento, CA clinical manufacturing facility focused on high-precision cell therapies. The Associate, Cell Therapy Production role involves executing GMP manufacturing runs, cleaning and maintaining equipment, and documenting activities in a regulated environment.

You will collaborate with QC, QA, and Materials Management to ensure compliant production and continuous improvement, while meeting strict quality standards and SOPs.

Qualifications

• BS or MS in biology or related field, with GMP familiarity.
• 1–2 years in process sciences, discovery or manufacturing.
• Aseptic techniques and cleanroom experience.

Responsibilities

• Operate and monitor automated equipment for cell processing, expansion, and filling in Grade B/C cleanrooms.
• Follow SOPs and batch records to perform production activities.
• Maintain quality documentation and participate in investigations and deviations.
• Collaborate with Materials Management, QC, and QA for GMP manufacturing runs.
• Support continuous improvement and on-call rotation as needed.

Skills

Visual acuity 20/20

Aseptic techniques

Attention to detail

Strong work ethic

Interpersonal skills

Team collaboration

Communication

Education

BS in Biology or related field

MS in Biology or related field

Tools

Automated manufacturing equipment

GMP documentation systems

Job description

Orca Bio operates a Sacramento, CA clinical manufacturing facility focused on high-precision cell therapies. The Associate, Cell Therapy Production role involves executing GMP manufacturing runs, cleaning and maintaining equipment, and documenting activities in a regulated environment.

You will collaborate with QC, QA, and Materials Management to ensure compliant production and continuous improvement, while meeting strict quality standards and SOPs.