QC Biochemist

job summary:
Join a Top-Tier Global Pharma Leader as an MCS Associate Quality Control. This 100% onsite role is a 1-year contract supporting the release and characterization testing of drug substances and products. We are seeking a self-starting professional with a strong foundation in GMP practices and bioassay execution to join our collaborative team in Thousand Oaks.

location: Newbury Park, California
job type: Contract
salary: $25.00 - 27.32 per hour
work hours: 9 to 5
education: High School

responsibilities:

• Execute cell-based potency assays and ligand-binding assays (e.g., ELISA) to support release, characterization, and stability testing.
• Perform core laboratory techniques including precise pipetting, preparation of serial dilutions, and reagent/standard preparation.
• Maintain and monitor cell cultures to ensure cell health and continuous assay readiness.
• Operate and maintain specialized laboratory equipment, including plate readers and automated liquid handling systems.
• Document all test results and laboratory activities in strict accordance with cGMP requirements and SOPs to ensure data integrity.
• Manage inventory of critical reagents and reference standards, coordinating ordering to meet production timelines.

 
qualifications:
Required:

• Bachelor's degree in Life Sciences (Biology, Chemistry, Biochemistry) or equivalent experience.
• Hands-on experience in a regulated QC/GMP laboratory environment (Pharma, Biotech, or Academia).
• Demonstrated proficiency in analytical testing, specifically ELISA or cell-based assays.
• Strong technical skills in pipetting, serial dilutions, and general assay setup.
• Ability to work Monday-Friday (8:00 AM - 5:00 PM) with occasional weekend overtime (~once a month).

Preferred:

• Experience using automated liquid handling systems.
• Proficiency in data entry within electronic laboratory notebooks and LIMS.
• Strong conflict resolution skills and ability to work effectively within a small, matrixed team.

#LI-PV1

skills: Good Laboratory Practices (GLP), Cell-based Assays, SOP Development, Good Manufacturing Practices (GMP), Quality Control (QC), Quality Control Testing


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on randstadusa.com.


Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).


This posting is open for thirty (30) days.

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.


Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.


We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.