Pharma Manufacturing Technician - GMP, 2nd/3rd Shift

Astrix Inc.; Fremont (CA); On-site; USD 33,000 - 34,000; Full time

Benefits offered by this job

Benefits included

Job summary

Astrix Inc. in Fremont, CA is hiring a Manufacturing Associate to join a global, research-driven pharmaceutical manufacturer focused on innovative treatments. The role supports assembly, packaging, filling, and materials movement on 2nd and 3rd shifts, with pay of $24–$25 per hour.

Candidates should have a High School Diploma and 1+ year of GMP-regulated experience; biotechnology experience is a plus. The position requires adherence to cGMP procedures and the ability to stand for extended

Qualifications

• High School Diploma or equivalent plus 1+ year of GMP-regulated experience.
• Pharmaceutical or biotechnology manufacturing experience preferred.
• Biotechnology training or an Associate's/Bachelor's degree is a plus.
• Strong attention to detail and ability to follow written procedures and cGMP requirements.
• Ability to stand and walk for extended periods.

Responsibilities

• Perform assembly, packaging, filling, visual inspection, and material movement.
• Support equipment setup, changeovers, troubleshooting, and minor adjustments.
• Gather and stock production materials, tools, and supplies.
• Complete batch records, logbooks, and other required documentation.
• Maintain a clean, safe, and organized production environment.
• Escalate production, equipment, quality, and safety issues as needed.

Skills

Attention to detail

Follow written procedures

GMP experience

Physical endurance

Education

High School Diploma or equivalent

Associate's/Bachelor's degree a plus

Job description

Astrix Inc. in Fremont, CA is hiring a Manufacturing Associate to join a global, research-driven pharmaceutical manufacturer focused on innovative treatments. The role supports assembly, packaging, filling, and materials movement on 2nd and 3rd shifts, with pay of $24–$25 per hour.

Candidates should have a High School Diploma and 1+ year of GMP-regulated experience; biotechnology experience is a plus. The position requires adherence to cGMP procedures and the ability to stand for extended