Manufacturing Associate I
The Manufacturing Associate I executes routine assembly and packaging operations in a GMP-regulated pharmaceutical manufacturing environment, supporting senior staff and ensuring compliance with standard operating procedures. The role involves equipment setup, minor repairs, documentation, and maintaining production area standards, contributing to efficient drug product manufacturing in a multi-product facility.
About Careertakes
👉 Important disclosure: Careertakes is a third-party recruiting platform supporting this hiring process. If selected, you will be employed directly by our client, Manufacturing — Biotechnology & Pharmaceutical.
Applicants for this role may also receive access to additional matched opportunities through the Careertakes platform.
What You’ll Do
This entry-level Manufacturing Associate I role supports assembly and packaging operations for drug product manufacturing in a multi-product facility for our Confidential Client. You will perform routine unit operations under limited supervision, assist senior staff, and follow cGMP and SOP requirements.
- Execute assembly and packaging tasks on automated and semi-automated equipment.
- Assist in setup, changeover, and minor troubleshooting of autoinjector assembly machines, pre-filled syringe assembly machines, and tabletop equipment.
- Retrieve components and tools from storage and ensure materials are stocked before operations.
- Document all activities accurately in controlled documents (batch records, logbooks, SOP attachments).
- Support visual inspection, filling, product/component movement, and cleanroom maintenance.
- Follow 5S and safety standards; identify and escalate unsafe conditions.
- Communicate clearly during shift hand-offs and assist relief personnel as required.
Qualifications & Skills
- Entry-level proficiency; 0–2 years preferred in GMP-regulated manufacturing.
- High school diploma required; Associate or Bachelor’s degree (or biotech vocational training) preferred.
- Minimum one (1) year work experience in a GMP-regulated industry preferred.
- Strong attention to detail and ability to follow written instructions.
- Basic math skills (addition, subtraction, multiplication, division, unit conversions).
- Good verbal and written communication; ability to work in small teams.
- Ability to learn basic computer functions (MS Office, Outlook) and follow computerized workflows.
- Willingness to obtain and maintain required qualifications and follow SOPs and cGMP practices.
Physical & Schedule Requirements
- Ability to stand for most of the shift and walk for prolonged periods.
- Schedule depends on assigned shift; regular attendance is required per company policy.
- Ability to perform routine material handling and light equipment movement.
Compensation & Location
- Pay Range: $19.51 — $24.51 per hour.
- Employment Type: Full-time.
- Job Location: Union City, CA (on-site).
- Employer: Confidential Client (manufacturing — biotechnology & pharmaceutical).
Why This Role?
- Gain hands-on experience in regulated manufacturing operations and medical device/drug-product assembly.
- Work with experienced production teams and grow technical skills in automated assembly and packaging.
- Competitive hourly pay with opportunities to develop additional qualifications.
Equal Opportunity & Hiring Transparency
Careertakes and our client are Equal Opportunity Employers committed to building a diverse and inclusive workforce. We prohibit discrimination or harassment of any kind. To support a fair and efficient hiring process, AI tools may be used to assist with application review or resume screening. These tools do not replace human decision-making. Final hiring decisions are made by people.
If you have questions about how your data is used, please contact us directly.
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