Chemist with HPLC & Protein Exp (Entry Level)

Job Title: MCS Associate Quality Control

Location: Thousand Oaks CA – 100% Onsite

Duration: 6 Months with possible extension.

Terms: Contract W2

Description:

Note:

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

Contract Duration: 6 months to start

Location: Thousand Oaks, CA (100% on-site)

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

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 with 2 YOE.

• 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.

• Strong fundamental laboratory skills with a demonstrated ability to accurately follow established laboratory procedures.

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. Lab performs compendial based testing (e.g. pH, Protein Concentration, Water Testing, Endotoxin, Appearance, Color, Clairty)

Key Responsibilities

• Perform routine laboratory procedures and analytical testing in a regulated QC environment

• Document, calculate, compile, interpret, and enter laboratory data accurately and in a timely manner

• Operate, maintain, and troubleshoot laboratory instruments and specialized equipment as required.

• Maintain laboratory reagents and maintain an inspection ready area

• Maintain complete and compliant laboratory documentation, including logbooks, worksheets, and electronic records

• Follow all applicable safety guidelines, cGMPs, and CFR requirements

• Maintain training records and comply with written procedures and laboratory systems

• Support controlled document updates and change implementation activities

• Identify and escalate compliance, safety, or data integrity issues as appropriate

• May recommend and implement improvements related to routine job functions