Manufacturing Associate I

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

Job summary

Astrix Technology in Fremont, California is seeking a Manufacturing Associate I to support drug product operations in a GMP environment. You will perform routine assembly and packaging tasks under supervision, and assist with equipment setup and documentation.

This entry-level role requires a high school diploma and an interest in biotech/pharmaceutical manufacturing. Training is provided, with shift options and a 15% shift differential for the 3rd shift.

Qualifications

• High school diploma required or equivalent.
• Bachelor's/associates degree preferred in biotech or related field.
• Experience in GMP-regulated environment is preferred.

Responsibilities

• Perform routine assembly and packaging tasks in a GMP drug manufacturing environment under limited supervision.
• Support with assembly and packaging activities in the designated production area.
• Assist with equipment troubleshooting, changeovers, and minor repairs.
• Set up autoinjector and syringe assembly equipment and semi-automated tabletop machines with required tools and documentation.
• Complete batch records, logbooks, and SOP attachments accurately; report events to supervisor.
• Maintain production areas per 5S standards including cleaning and sanitization.
• Verify calibration and complete required logbooks.
• Support visual inspection and filling operations as needed.
• Ensure components, materials and supplies are stocked ahead of operations.
• Move product, components, and equipment within the assembly, packaging, and CNC areas.
• Communicate effectively with relief personnel during shift change.
• Identify unsafe conditions and escalate appropriately.

Skills

Organizational skills

Mathematical skills

Attention to detail

SOP adherence

Education

High school diploma

Associate's or Bachelor's degree preferred

Tools

MS Office

Outlook

Job description

Manufacturing Associate I

Manufacturing

Fremont, California, US

• Added - 17/08/2026

Pay Rate Low: 24 | Pay Rate High: 25

Position Overview

We are partnering with a growing multi-product pharmaceutical manufacturing facility to place Manufacturing Assembly & Packaging Associates supporting drug product operations. This is a great opportunity for an entry-level candidate with GMP exposure to join a structured team performing assembly, packaging, and equipment support functions under the guidance of senior associates.

Shift

3rd Shift, beginning 8/24/2026 through 12/30/2026 (facility shutdown in late December). A subset of the team will be asked to return on 2nd Shift (Monday-Friday, 2:00 PM-10:30 PM) through the end of the following year, based on team fit.

Compensation

$24-$25/hr Shift Differential: 15%, effective first day of work

What You'll Do

• Perform routine assembly and packaging tasks in a multi-product drug manufacturing environment under limited supervision, following standard operating procedures.
• Support Senior and Master Associates with assembly and packaging activities in the designated production area.
• Assist with equipment troubleshooting, changeovers, and minor repairs or adjustments.
• Help set up automated autoinjector and pre-filled syringe assembly equipment, as well as semi-automated tabletop machines, including gathering tools, parts, and required documentation.
• Complete all documentation accurately in batch records, logbooks, and SOP attachments; report events and issues to the production supervisor.
• Maintain production areas in accordance with 5S standards, including cleaning, waste removal, and sanitization.
• Verify equipment calibration and complete required logbooks.
• Support visual inspection and filling operations as needed.
• Ensure components, materials, and supplies are stocked ahead of operations.
• Move product, components, and equipment within the assembly, packaging, and CNC areas.
• Communicate effectively with relief personnel during shift change.
• Identify and escalation unsafe conditions or practices appropriately.

What We're Looking For

• High school diploma plus a minimum of one (1) year of experience in a GMP-regulated industry.
• Associate's or Bachelor's degree, or biotechnology vocational training, preferred.
• Prior experience in a GMP environment within biotechnology or pharmaceuticals strongly preferred.
• Strong organizational skills and ability to work effectively in small teams.
• Basic mathematical skills, including addition, subtraction, multiplication, division, and conversions.
• Strong attention to detail with the ability to read, comprehend, and follow written instructions.
• Basic computer proficiency, including MS Office and Outlook.
• Willingness to adhere to all SOPs, cGMP requirements, and company policies and procedures.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

#INDBH

#LI-DNI

Position Overview

We are partnering with a growing multi-product pharmaceutical manufacturing facility to place Manufacturing Assembly & Packaging Associates supporting drug product operations. This is a great opportunity for an entry-level candidate with GMP exposure to join a structured team performing assembly, packaging, and equipment support functions under the guidance of senior associates.

Shift

3rd Shift, beginning 8/24/2026 through 12/30/2026 (facility shutdown in late December). A subset of the team will be asked to return on 2nd Shift (Monday-Friday, 2:00 PM-10:30 PM) through the end of the following year, based on team fit.

Compensation

$24-$25/hr Shift Differential: 15%, effective first day of work

What You'll Do

• Perform routine assembly and packaging tasks in a multi-product drug manufacturing environment under limited supervision, following standard operating procedures.
• Support Senior and Master Associates with assembly and packaging activities in the designated production area.
• Assist with equipment troubleshooting, changeovers, and minor repairs or adjustments.
• Help set up automated autoinjector and pre-filled syringe assembly equipment, as well as semi-automated tabletop machines, including gathering tools, parts, and required documentation.
• Complete all documentation accurately in batch records, logbooks, and SOP attachments; report events and issues to the production supervisor.
• Maintain production areas in accordance with 5S standards, including cleaning, waste removal, and sanitization.
• Verify equipment calibration and complete required logbooks.
• Support visual inspection and filling operations as needed.
• Ensure components, materials, and supplies are stocked ahead of operations.
• Move product, components, and equipment within the assembly, packaging, and CNC areas.
• Communicate effectively with relief personnel during shift change.
• Identify and escalation unsafe conditions or practices appropriately.

What We're Looking For

• High school diploma plus a minimum of one (1) year of experience in a GMP-regulated industry.
• Associate's or Bachelor's degree, or biotechnology vocational training, preferred.
• Prior experience in a GMP environment within biotechnology or pharmaceuticals strongly preferred.
• Strong organizational skills and ability to work effectively in small teams.
• Basic mathematical skills, including addition, subtraction, multiplication, division, and conversions.
• Strong attention to detail with the ability to read, comprehend, and follow written instructions.
• Basic computer proficiency, including MS Office and Outlook.
• Willingness to adhere to all SOPs, cGMP requirements, and company policies and procedures.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

#INDBH

#LI-DNI

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.