Quality Control Chemistry Associate

Now Hiring: Quality Control Chemistry Associate

Location: Santa Ana, CA area

Advantage Technical is hiring an experienced Quality Control Chemistry Associate. Join the team today where your skills in HPLC/UPLC analysis, GMP compliance, and chemical testing will directly support nationwide product distribution.

Qualifications

• A bachelor's degree in chemistry or related scientific discipline
• 2+ years of laboratory experience in a pharmaceutical, biotech, or medical device setting
• Proficient in chromatographic techniques (UPLC, HPLC, GC/MS, ICP/MS)
• Solid understanding of FDA, GLP, GMP, and USP guidelines
• Skilled in statistical data analysis and laboratory best practices
• Strong written and verbal communication, organizational, and time-management skills
• Ability to work independently and collaboratively in a fast-paced lab environment

Technical & Software Skills

• UPLC / HPLC / GC-MS / ICP-MS / HLPC-MS
• Microsoft Office Suite (Excel, Word, PowerPoint)
• Data analysis and laboratory information systems (LIMS)
• Project management and documentation software

Physical & Work Requirements

• Ability to stand, sit, stoop, and perform repetitive lab tasks
• Capable of lifting and handling up to 40 pounds
• Comfortable working in controlled lab environments with protective gear and equipment
• Occasional travel may be required

Position Overview

As a Quality Control Chemistry Associate, you will conduct both quantitative and qualitative analyses of finished pharmaceutical products, raw materials, and environmental samples. Your work ensures product quality, safety, and regulatory compliance with cGMP, GLP, and 21 CFR Part 11 standards. You'll collaborate closely with senior chemists to evaluate drug potency trends, support deviation investigations, and contribute to method development and validation.

Key Responsibilities

• Conduct HPLC/UPLC chemical testing and analysis on pharmaceutical products and raw materials
• Review, interpret, and document analytical data, chromatograms, and lab reports
• Assist in method validation and instrument troubleshooting (e.g., UPLC, HPLC, GC/MS)
• Prepare reagents and standards in compliance with USP and internal SOPs
• Investigate product deviations, non-conformances, and customer complaints
• Present technical findings, trends, and investigative reports to management
• Support internal audits and regulatory inspections (FDA, DEA, BOP, etc.)
• Maintain strict data integrity and ensure documentation adheres to GMP standards

Employee Benefits

• Medical, dental, vision, and pet insurance
• 401(k) Retirement Savings Plans
• Employee Assistance Program (EAP)
• Commuter/Parking Accounts
• People Perks
• Health Savings Account (HSA)
• AD & D Insurance

Pay | $27.58 - $29.05 per hour

Ready to advance your chemistry career in a high-impact pharmaceutical setting? Click "Apply Now" and take the next step in joining a quality-driven team committed to scientific excellence and public health.

The base pay range above represents the low and high end of the base compensation range we reasonably expect to pay for this position. Actual base compensation will vary and may be above or below the range based on various factors including, but not limited to, geographic location, actual experience, and job performance. This job posting is not a promise of any specific pay for any specific employee.

The range listed is just one component of the total compensation package for our employees. Based on the details of your position, we provide a variety of benefits to our employees, including medical, dental, and vision plans, pre-tax savings plans, pre-tax parking and commuter plans, supplemental health and welfare plans, a retirement savings plan, an employee assistance program, pet insurance, and paid holidays. Other rewards may include short-term incentives and paid time off.

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