Quality Control Associate

Aequor; Thousand Oaks (CA); On-site; USD 34,440 - 37,195; Full time

Job summary

A leading biotechnology company in Thousand Oaks, CA, is looking for an early-career professional for routine laboratory testing and Quality Control operations. Candidates should have a degree in Biological sciences or equivalent experience in QC GMP. Strong reliability, time management, and a collaborative attitude are essential. The role involves working under general supervision and adhering to safety guidelines and regulatory requirements. This is a contract position scheduled from Monday to Friday with a pay range of $25-$27 per hour.

Qualifications

• Recent graduate or candidate with hands-on QC GMP experience.
• Eager to learn analytical testing techniques.
• Comfortable with documentation systems.

Responsibilities

• Perform routine laboratory testing in support of Quality Control operations.
• Adhere to cGMP and safety guidelines.
• Support analytical testing and documentation.

Skills

Reliability

Time management

Collaborative attitude

Basic computer skills

Education

Bachelor’s in Biology, Chemistry, Biochemistry, or related field

Job description

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

Base pay range

$25.00/hr - $27.00/hr

Location: Thousand Oaks, CA

Terms: Contract W2

Duration: 12 Months Contract (Will Get Extended for Long)

Schedule: Monday–Friday, 8:00 AM–5:00 PM

Candidate must be someone near the office or can travel to the office without any problem.

Recruitment Consultant at Aequor Technologies | Pharma & Biotech Industry

The ideal candidate for this role is:

• A recent graduate (or early-career professional) with a Bachelor’s in Biology, Chemistry, Biochemistry, or related field, OR a candidate with hands‑on QC GMP experience who may not hold a degree.
• Highly trainable and eager to learn analytical testing techniques in a regulated QC lab.
• Brings strong reliability, time management, and a collaborative attitude to the team.
• Comfortable with basic computer skills and documentation systems.
• Familiarity with GMP principles is a plus, but not a strict requirement.

Job Summary

Under general supervision, this position performs routine laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good Manufacturing Practices (cGMP), safety guidelines, and regulatory requirements while supporting analytical testing, documentation, and laboratory operations.