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MCS Associate Quality Control
Contract: Thousand Oaks, California, US span>
Salary Range: 28.00 - 29.00 | Per Hour
Job Code: 371606
End Date: 2026-10-11
Days Left: 26 days, 20 hours left
- The role is 100% onsite in Thousand Oaks and follows a standard Monday–Friday 8 AM – 5 PM schedule.
- The ideal candidate will have a bachelor’s degree in a scientific discipline and prior academic or industry laboratory experience.
- They should be familiar with basic lab techniques including pipetting, weighing, calculations and dilutions, and be comfortable working in a GMP-regulated environment.
- Experience with multichannel pipetting and ELISA experience is a plus, but not required, as full training will be provided.
- Strong attention to detail, good documentation practices (GDocP), and comfort with lab notebooks and electronic systems are essential.
Job Details:
- Under general supervision, this position will perform routine procedures and testing in support of the lab.
- This position will be responsible for one or more of the following activities:
- Performing routine laboratory procedures
- Routine analytical testing
- Documenting, computing, compiling, interpreting, and entering data
- Maintaining and operating specialized equipment
- Initiating and / or implementing changes in controlled documents.
- Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.
- Preferred Qualifications Ability to adhere to regulatory requirements, written procedures and safety guidelines.
- Ability to evaluate documentation/data according to company and regulatory guidelines Ability to organize work, handle multiple priorities and meet deadlines.
- Strong written and oral communication skills.
- Must be detail orientated.
- Must be flexible and adaptable to changing priorities and requirements. Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance.
- Demonstrates understanding of when and how to appropriately escalate.
- May identify, recommend and implement improvements related to routine job functions. Must learn and comply with safety guideline and cGMPs.
Job Requirement
- Pipetting
- ELISA
- GDocP
Reach Out to a Recruiter
- Recruiter
- Phone
- sakshi malviya
- sakshi.malviya@collabera.com