Quality Control Analyst I

Kelly Services; Lodi (CA); On-site; USD 34,000 - 49,000; Full time

Job summary

Kelly Science & Clinical is seeking a Quality Control Analyst I for a premier client in Lodi, CA. This role tests finished products and ensures compliance with GMP standards and FDA/ISO regulations, offering growth in a regulated laboratory environment.

The position focuses on documenting testing, data analysis against product specs, and contributing to continuous improvement across QC processes and lab operations; weekend/overnight schedule is required.

Qualifications

• High School Diploma (or equivalent) and at least 1 year of related experience, or an AA/Technical Trade Degree.
• Comfortable working in a fast-paced, high-throughput laboratory environment.
• Prior experience handling biological and chemical materials.
• Experience working in a GMP-compliant environment.

Responsibilities

• Perform and document laboratory testing of finished products per established procedures
• Analyze data based on product specifications and standardized methods
• Participate in continuous improvement efforts across QC processes, lab operations, and work environment

Education

High School Diploma (or equivalent)

AA/Technical Trade Degree

Job description

Kelly® Science & Clinical is seeking a Quality Control Analyst I for a premier client in Lodi, CA. This is a great opportunity to join an innovative molecular and diagnostics manufacturing company and gain valuable industry experience in a regulated laboratory setting.

Job Title:

Quality Control Analyst I

Schedule:

Sunday Through Wednesday, alternating Saturdays | 6:00 PM - 6:00 AM

Pay Rate:

$30.32/hour (this includes a night shift differential)

Position Summary:

The Quality Control Analyst I is responsible for finished product testing activities in accordance with GMP standards and FDA/ISO regulations. This role offers the opportunity to develop laboratory skills, support process efficiency initiatives, and pursue long-term growth within the quality control department.

Key Responsibilities:

• Perform and document laboratory testing of finished products per established procedures
• Analyze data based on product specifications and standardized methods
• Participate in continuous improvement efforts across QC processes, lab operations, and work environment

Minimum Qualifications:

• High School Diploma (or equivalent) and at least 1 year of related experience, or an AA/Technical Trade Degree
• Comfortable working in a fast-paced, high-throughput laboratory environment

Preferred Qualifications:

• Prior experience handling biological and chemical materials
• Experience working in a GMP-compliant environment

Important Application Note:

The Kelly® Recruiter will ask for your Month and Day of Birth (not the year) to submit your application into the client's system. This is a required step in the process.

What Happens Next:

Once you apply, you’ll move forward if your skills and experience align with the role. And even if this opportunity isn’t the right fit, you’ll remain part of the Kelly® Science & Clinical network for future openings tailored to your background.