Pharmaceutical Manufacturing Associate

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

Job summary

Astrix is seeking a Manufacturing Associate for its Fremont, CA facility to support assembly, packaging, filling, and inspection tasks.

The role requires GMP experience and a High School diploma, with biotech education a plus. Candidates should be able to stand for long periods and follow strict procedures. The position offers scheduled 2nd or 3rd shifts and a contract with extension potential.

Qualifications

• High School Diploma or equivalent with 1+ year GMP experience.
• Pharma/biotech 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

GMP experience

Pharmaceutical manufacturing

Detail oriented

Procedures follow

Education

High School Diploma or equivalent

Associate's/Bachelor's degree is a plus

Job description

Pay Rate Low: 24.00 | Pay Rate High: 25.00

Join a global, research-driven pharmaceutical manufacturer and help support the production of innovative treatments for patients with unmet medical needs.

Manufacturing Associate

Location: Fremont, CA

Contract With Potential To Extend (benefits Included)

Pay Rate: $24-$25/hr

Available Shifts

• 2nd Shift: Monday–Friday, 2:00 PM–10:30 PM
• 3rd Shift: Monday–Friday, 10:00 PM–6:30 AM

Key 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.

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.