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MCS Associate Quality Control
Career Insights for Quality Assurance Auditor
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Scorecard
Based on California data
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What they do
A Quality Assurance Auditor regularly evaluates the quality control systems in place and verifies compliance with quality and safety standards.
$57,451 / year median in California
-4% projected decline
Job Description
Job Description
MCS Associate Quality Control Contract:
Thousand Oaks, California, US Salary Range:
28.00 - 29.00 |
Per Hour Job Code:
371606
End Date:
2026-10-11
Days Left:
29 days, 8 hours left Position
Details:
-
Job Title:
MCS Associate Quality Control
Location:
Thousand Oaks CA Duration:
12 months
Description:
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.
Salary and
Other Compensation:
The annual [salary/hourly rate] for this position is between $28.00 - 29.00 per hour. Factors which may affect pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.
Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements:
[medical insurance], [dental insurance], [vision insurance], [401(k) retirement plan], [life insurance], [long-term disability insurance], [short-term disability insurance],
[paid parking/public transportation], [Paid time off], [Days/hours of paid sick and safe time], [Days/hours of paid vacation time], [Weeks of paid parental leave], [Paid holidays annually], [any additional benefits applicable]. Job Requirement
Pipetting
ELISA
GDocP
Reach Out to a Recruiter
Recruiter
Phone
sakshi malviya
sakshi.malviya@collabera.com
Benefits
- Paid Time Off (PTO)
- Sick Leave
- 401(k) Plans
- Other Retirement and Savings