Quality Control Research Associate II

R&D Partners; Santa Monica (CA); On-site; USD 41,052 - 51,329; Full time

Benefits offered by this job

Medical insurance – PPO, HMO & HSA

401k plan

Employee Assistance Program

Long-term disability

Weekly payroll

Online timecard approval

Job summary

Join a dynamic pharmaceutical company as a Quality Control Research Associate II. In this role, you will be integral to ensuring product quality through non-routine analysis of raw materials and finished products. Your expertise in Quality Control Analytical Testing will be essential as you evaluate equipment, maintain compliance, and assist in training staff. This position offers a unique opportunity to contribute to a leading firm in the pharmaceutical industry, where your skills will help shape the future of healthcare. Enjoy a comprehensive benefits package and a supportive work environment that values your contributions and fosters professional growth.

Qualifications

• 2+ years of experience in Quality Control Analytical Testing in a GMP environment.
• Bachelor's degree in a scientific discipline required.

Responsibilities

• Evaluate and install new equipment, ensuring compliance with regulations.
• Troubleshoot instrumentation and maintain laboratory standards.

Skills

Quality Control Analytical Testing

Good Manufacturing Practices (cGMP)

Good Laboratory Practices (GLP)

Troubleshooting

Microsoft Office

Education

Bachelor's degree in scientific discipline

Tools

ELISA

Flow Cytometry

PCR

Job description

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This range is provided by R&D Partners. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$29.80/hr - $37.26/hr

Pharmaceutical company is hiring a Quality Control Research Associate II for a 6-month contract. You will conduct non-routine analysis of raw materials, intermediates, and finished product samples.

Responsibilities

• Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
• Perform reviews of assays and maintain laboratory in a state of compliance.
• Troubleshoot instrumentation and test methods.
• Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs).
• Writes and executes protocols and SOPs.
• Assists in the training of QC staff as needed.

Qualifications

• Bachelor's degree in scientific discipline.
• 2+ years of Quality Control Analytical Testing experience (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
• Working knowledge and proficiency with Microsoft Office software.

Pay

$29.80-$37.26/hr

Why Choose R&D Partners?

As an employee, you have access to a comprehensive benefits package including:

• Medical insurance – PPO, HMO & HSA
• 401k plan
• Employee Assistance Program
• Long-term disability
• Weekly payroll
• Online timecard approval

R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

R&D Partners is an equal-opportunity employer.

Seniority level

Associate

Employment type

Full-time

Job function

Research

Industries

Staffing and Recruiting and Pharmaceutical Manufacturing